• Accurately store and organize products within the warehouse.
• Prepare customer orders for shipment according to established processes and procedures.
• Label and meter packages using various freight and shipping systems.
• Process orders accurately using the client's ERP system.
• Complete daily preparations for the following day's shipping activities.
• Maintain a safe, organized, and clean warehouse environment.
• Follow established warehouse safety procedures and operational standards.
• Support divisional initiatives as directed by management.
• Follow applicable Quality Management System (QMS), Environmental Management System (EMS), and other regulatory requirements.

• High school diploma or equivalent required.
• Strong attention to detail and commitment to order accuracy.
• Ability to follow established warehouse, shipping, and safety procedures.
• Dependable and able to work effectively in a fast-paced distribution environment.
• Ability to maintain an organized and clean work area.
• Experience with warehouse, shipping, distribution, freight, or ERP systems is beneficial.

Senior Cell Therapy Scientist

•  Develop, optimize, and transfer analytical methods for cell therapy product characterization and release using Design of Experiments (DoE). 
•  Design and execute exploratory studies to define critical quality attributes (CQAs) and improve analytical assays. 
•  Independently plan, execute, analyze, and interpret experimental data while recommending next steps. 
•  Perform analytical method risk assessments and implement improvements for robustness and regulatory compliance. 
•  Execute laboratory experiments and collaborate with junior scientists to generate high-quality analytical data. 
•  Analyze, summarize, and present scientific findings to cross-functional stakeholders. 
•  Support analytical method development, transfer, qualification, and lifecycle management for process development, product release, and stability testing. 
•  Trend assay performance data and establish appropriate analytical controls. 
•  Author SOPs, technical reports, qualification documentation, and regulatory submission materials. 
•  Collaborate with cross-functional development teams supporting cell therapy programs. 
•  Mentor and train junior laboratory personnel as needed. 
•  Ensure compliance with cGMP, Good Documentation Practices (GDP), Good Laboratory Practices (GLP), and applicable regulatory requirements. 

•  Master's degree in Immunology, Molecular Biology, Biochemistry, or related scientific discipline with 6-9+ years of industry experience in analytical development, QC, technology transfer, or analytical method lifecycle management OR
•  Ph.D. in a related scientific field with 2+ years of relevant industry experience. 
•  Extensive experience with flow cytometry and immunology-based analytical method development. 
•  Experience transferring analytical methods to QC laboratories. 
•  Demonstrated expertise in: 
  •  Analytical method optimization and remediation 
  •  CMC technology transfer 
  •  Analytical control strategies 
  •  Method qualification and validation 
•  Strong knowledge of Design of Experiments (DoE), statistical data analysis, capability assessments, and control charts. 
•  Working knowledge of ICH guidelines, USP, cGMP regulations, and industry best practices. 
•  Strong analytical thinking, troubleshooting, and problem-solving skills. 
•  Excellent written and verbal communication skills. 
•  Ability to manage multiple projects in a fast-paced environment. 
•  Commitment to laboratory safety and quality documentation. 

•  2+ years of cell therapy industry experience. 
•  Experience supporting stem cell or T-cell analytical control systems. 
•  Experience with one or more of the following: 
  •  ddPCR 
  •  qPCR 
  •  Cell imaging 
  •  Reporter-based potency assays 
  •  Cell engineering 
  •  Next-Generation Sequencing (NGS) 
  •  Metabolic analysis 

• Location: San Diego, California (Onsite) 
• Duration: 5-Month Contract 
• Employment Type: W-2 Only 
• No C2C
• Pay Rate: $60.00-$68.97/hour (DOE) 

• Ensure products are accurately received, organized, and stored within the warehouse.
• Accurately prepare customer orders for shipment according to established processes and procedures.
• Label, meter, and prepare packages using various freight and shipping systems.
• Process orders using the ERP system.
• Maintain a safe, clean, and organized warehouse environment.
• Complete daily preparations for the following day's shipping activities.
• Support divisional initiatives as identified by management.
• Follow applicable Quality Management System (QMS), Environmental Management System (EMS), and other regulatory requirements.
• Perform additional warehouse and shipping duties as assigned.

• High School Diploma or equivalent required.
• Ability to work accurately in a fast-paced warehouse/distribution environment.
• Strong attention to detail and ability to follow established procedures.
• Dependable and able to work the scheduled shift of 12:00 PM – 8:30 PM.
• Previous warehouse, shipping, distribution, ERP, or freight-system experience is beneficial.

• Closed-toe shoes must be worn at all times.
• Long pants are required; shorts are not permitted.
• Pants must be worn at waist level so undergarments are not visible.
• Hats of any type are prohibited.
• Hooded sweatshirts are permitted, but hoods must remain down.
• Tank tops and cutoff shirts are prohibited.
• Clothing displaying slogans, pictures, words, or images that could be interpreted as offensive is prohibited.
• Sunglasses may not be worn on the distribution center floor.

•  Coordinate the preparation, publishing, and submission of regulatory documentation for product registrations, primarily within the U.S. and EU markets. 
•  Prepare regulatory submissions in accordance with applicable Health Authority guidelines and internal standards and procedures. 
•  Format, publish, and perform quality reviews of regulatory documents to ensure compliance with submission requirements. 
•  Collaborate with Regulatory Leads, Managers, project leads, and cross-functional teams to gather required documents and information. 
•  Ensure regulatory submission deliverables are complete, accurate, and delivered according to established timelines. 
•  Maintain tracking systems to monitor submission status, milestones, deliverables, and deadlines. 
•  Support the management and maintenance of regulatory publication databases, repositories, and document management systems. 
•  Navigate U.S. Health Authority portals and other regulatory submission systems as required. 
•  Coordinate with internal stakeholders to facilitate efficient and timely submission activities. 
•  Manage multiple regulatory publishing projects simultaneously while maintaining a high level of accuracy. 
•  Maintain organized and compliant regulatory documentation throughout the submission lifecycle. 
•  Support compliance with applicable regulatory guidelines, internal procedures, and documentation standards. 

•  Bachelor's degree in Life Sciences, Regulatory Science, Quality, or a related field, or equivalent professional experience. 
•  Minimum of 5 years of experience in regulatory submission publishing or a closely related regulatory function. 
•  Proven experience preparing compliant regulatory submissions within the diagnostics, pharmaceutical, biotechnology, or life sciences industry. 
•  Experience supporting regulatory submissions for the U.S. and/or European Union markets. 
•  Familiarity with regulatory guidelines and requirements, including FDA, EMA, ICH, and GxP. 
•  Strong understanding of regulatory document preparation, formatting, publishing, and submission processes. 
•  Excellent attention to detail and organizational skills. 
•  Strong written and verbal communication skills. 
•  Ability to manage multiple projects, priorities, and deadlines in a fast-paced environment. 
•  Ability to collaborate effectively with Regulatory Affairs professionals, project teams, and cross-functional stakeholders. 

•  Microsoft Word 
•  Adobe Acrobat Pro 
•  ISI Toolbox 
•  Veeva RIMS 
•  U.S. Health Authority portals 
•  Document Management Systems (DMS) 
•  Gmail and Chat 
•  Industry-standard regulatory publishing and submission tools 

•  Previous experience within a diagnostics, pharmaceutical, or biotechnology organization. 
•  Advanced experience with regulatory publishing and submission software. 
•  Experience with Veeva RIMS and regulatory document management systems. 
•  Experience navigating U.S. Health Authority submission portals. 
•  Knowledge of FDA and EU regulatory submission expectations. 
•  Demonstrated ability to independently coordinate multiple regulatory publishing deliverables and deadlines. 

• Execute FAR 15 subcontracts in accordance with FAR, DFARS, and applicable regulations.
• Develop strong negotiation strategies for contract execution.
• Manage key program suppliers.
• Train and mentor team members.
• Build supplier strategies to deliver best value.
• Deliver compliant FAR 15 proposal packages to government customers.
• Partner closely with Pricing to ensure compliant submissions.
• Negotiate FAR 15-compliant subcontracts with suppliers.

• High School Diploma or GED required.
• 3–5 years of experience in: Sourcing, Procurement, Supply Chain, Law & Contracts (L&C) and/or Business or Finance.
• Experience with FAR 15 subcontracting.
• Strong attention to detail and ability to manage multiple tasks simultaneously.
• Excellent communication and interpersonal skills.
• Strong negotiation capabilities and processes.

• Bachelor’s degree.
• Experience working with subcontractors across the full program lifecycle.
• Knowledge of Federal Acquisition Regulations (FAR) and DFARS.
• Experience with: MS Office Suite, SAP and/or other subcontract management tools
• Supply chain and procurement experience in defense, aerospace, or similar industries.
• Experience managing the following contract types: FFP (Firm Fixed Price), CP (Cost Plus) and CPIF (Cost Plus Incentive Fee).
• Experience with Truthful Cost or Pricing Data (TCPD).
• Ability to review and negotiate terms and conditions.
• Ability to work independently.

1. Walk me through a recent FAR 15 procurement you led—from RFP/proposal through negotiation and award. How did you ensure compliance with FAR/DFARS and Truthful Cost or Pricing Data (TCPD) while partnering with Pricing and suppliers to deliver a compliant package on schedule?
2. Describe a complex supplier negotiation involving FFP, CP, or CPIF subcontracts. How did you develop your negotiation strategy and balance value, compliance, and supplier relationships?
3. Provide an example of mentoring team members through a tight-deadline proposal or audit preparation. How did you ensure compliance, delegation, and on-time delivery?

• Plan and execute laboratory activities with a high degree of independence, applying scientific knowledge to support Culture Collection and panel production initiatives.
• Under minimal supervision, execute assigned project activities using established procedures and apply scientific knowledge and accumulated experience to complete projects involving the manipulation of human cell lines, microorganisms, and/or other biological materials.
• Perform nucleic acid extraction, including DNA, RNA, and plasmid extraction, quantification, and standard recombinant cloning techniques.
• Grow bacterial cultures under sterile conditions to ensure successful transformation and plasmid propagation.
• Generate, characterize, and manage biological materials that support assay development, clinical studies, and product development activities.
• Analyze experimental data, troubleshoot technical challenges, and recommend solutions to support project objectives.
• Lead small- to moderate-complexity projects by coordinating activities, managing timelines, and communicating progress with stakeholders.
• Maintain accurate electronic laboratory records within validated systems, including LIMS and electronic laboratory notebooks (eLN), ensuring compliance with quality and regulatory requirements.
• Contribute to scientific reports, technical documentation, presentations, and knowledge-transfer activities across cross-functional teams.
• Support laboratory operations through equipment maintenance, inventory management, biosafety compliance, and continuous improvement initiatives.
• Perform all work in accordance with established safety, quality, and regulatory requirements, including OSHA, ISO, and QSR standards.

• Bachelor’s degree in Microbiology, Molecular Biology, Cell Biology, or a related scientific discipline with 4+ years of relevant industry experience, or a master’s degree with 2+ years of relevant experience.
• Experience performing microbiological techniques, mammalian cell culture, molecular biology, and aseptic laboratory practices.
• Comfortable working with diverse biological materials, including microorganisms, mammalian cell lines, and human-derived specimens in a BSL-2 laboratory environment.
• May work with a variety of infectious human materials, including HxV, pathogenic bacteria, or engineered materials, and sample types such as blood, serum, urine, and stool.
• Familiarity with bacterial enumeration, MPN methods, MALDI-TOF identification, microbial taxonomy, and characterization techniques.
• Ability to maintain high-quality laboratory documentation and an understanding of data integrity, Good Laboratory Practices (GLP), and validated laboratory systems such as LIMS and electronic laboratory notebooks (eLN).
• Ability to independently plan laboratory work, manage multiple priorities, and solve scientific and technical challenges.
• Comfortable performing routine laboratory activities, including plating, pipetting, labeling, stocking, and vialing biological materials.
• Ability to work in collaborative, cross-functional environments and partner with diverse stakeholders to achieve shared scientific goals.
• Commitment to continuous learning, scientific excellence, and supporting process improvements that enhance laboratory efficiency and quality.

• Experience with automated laboratory workflows or high-throughput systems.
• Experience supporting platform or assay development.
• Project management experience, including coordinating timelines and stakeholder communications.
• Client-facing or customer-support experience.
• Strong analytical, organizational, communication, and problem-solving skills.
• Experience working effectively within a global, matrixed organization.

• Support the technical service and repair of Transmitters.
• Perform assigned assembly-line activities.
• Work with HLA and Return Kits.
• Decontaminate external medical devices using alcohol wipes.
• Use basic computer skills to support assigned work activities.
• Follow established work instructions and processes.
• Maintain dependable attendance and satisfactory job performance.
• Participate in provided training to learn the role’s processes and expectations.

• High school diploma.
• Basic computer skills.
• Ability to perform assembly-line and device-handling activities.
• Willingness to work with the decontamination of external medical devices using alcohol wipes.
• Willingness and ability to complete job-related training.

• Previous work experience in a production, assembly, repair, service, or similar environment.
• Medical device industry experience.
• Experience working with small devices, returned products, kits, or assembly-line processes.

• Receive, stock, organize, and replenish inventory using FIFO (First-In, First-Out) inventory practices.
• Pull, verify, and stage materials according to production orders.
• Deliver materials and supplies to production areas as needed.
• Count and verify materials for kitting operations to ensure inventory accuracy.
• Learn and maintain knowledge of stock locations throughout both the 1st and 2nd floor warehouse areas.
• Safely operate pallet jacks to transport materials.
• Maintain accurate inventory records with clear, legible handwriting and attention to detail.
• Keep warehouse, workstations, and equipment clean and organized.
• Follow established warehouse procedures, work instructions, and safety regulations.
• Support the orderly production and distribution of finished goods.
• Comply with U.S. Food and Drug Administration (FDA) regulations, company policies, operating procedures, and quality standards.
• Maintain positive working relationships with employees, customers, contractors, and vendors.
• Perform additional duties as assigned

• Previous warehouse, material handling, stocking, or inventory experience preferred.
• Experience using pallet jacks.
• Understanding of FIFO inventory management.
• Ability to accurately count and verify inventory and materials.
• Strong attention to detail and organizational skills.
• Clear handwriting and basic written documentation skills.
• Good verbal communication and teamwork abilities.
• Ability to follow standard operating procedures and work instructions.
• Willingness to learn warehouse layouts and stock locations.
• Ability to lift, move, and transport materials throughout the workday.
• Commitment to workplace safety and quality standards.
• Experience working in a regulated manufacturing or FDA environment is a plus.

• Manage the ETE IVDR/MDR product verification process for distributed products.
• Determine product requirements and controls.
• Complete objective evidence of supplier evaluation and approval.
• Manage Supplier Corrective Action Requests (SCARs) and ensure timely completion.
• Address supplier gaps by tracking robust corrective action plans.
• Complete supplier onboarding activities.
• Monitor supplier performance.
• Plan and follow up on supplier audits.
• Ensure supplier actions adequately resolve quality issues and are completed in a timely manner.
• Identify and escalate issues as they arise and provide appropriate solutions.

• Education: Bachelor’s or Master’s degree in Life Science, Data Science, or a related field, or equivalent experience.
• Two or more years of experience in Quality or a related function.
• Professional experience in a similar role within the medical device sector.
• Knowledge of deviation and resolution management.
• Expertise in quality systems, standards, and regulations, specifically production and/or supplier development processes and standards, including ISO 13485 and ISO 27001.
• Strong analytical skills with a focus on essential facts.
• Excellent communication skills.
• Cultural awareness and experience working with global internal and external partners and suppliers.
• Leadership mindset with the ability to lead others within an agile organization.
• Willingness and flexibility to collaborate across global teams in different time zones, including early working hours to support collaboration with colleagues in the European Union.
• Decisive with the ability to initiate and complete daily activities and proactively find solutions independently with limited guidance.

• Pick, fill, package, and prepare customer orders accurately and efficiently.
• Use an RF handheld scanner to process orders and track inventory.
• Perform inventory counts and help maintain accurate stock records.
• Verify part numbers, lot numbers, quantities, and product information.
• Support shipping and receiving activities, including package handling.
• Maintain established productivity, quality, and attendance standards.
• Follow all safety procedures and warehouse operating guidelines.
• Keep assigned work areas clean, organized, and free of hazards.
• Communicate and collaborate positively with coworkers and supervisors.
• Sit, stand, walk, reach, stoop, kneel, and crouch as required.
• Stand and walk for extended periods throughout the shift.

• At least two years of warehouse, distribution, or order-fulfillment experience.
• Knowledge of shipping and receiving procedures.
• Experience picking, pulling, filling, and packaging orders.
• Experience using an RF handheld scanner.
• Ability to accurately identify part numbers and lot numbers.
• Strong attention to detail and commitment to inventory accuracy.
• Ability to meet and maintain performance, quality, safety, and attendance expectations.
• Ability to work effectively in a team-oriented warehouse environment.
• Ability to perform the physical requirements of the position throughout the scheduled shift.

• Forklift experience.
• Additional experience with shipping and receiving operations.
• Experience conducting inventory counts.
• Experience identifying and tracking lot-controlled inventory.

• Perform functional evaluations across multiple engine models and part families, including the identification of engine boundary conditions and design requirements.
• Conduct 3D finite element thermal, stress, and modal analyses.
• Conduct strength, vibration, stress rupture, deflection, and life evaluations.
• Provide problem-solving guidance to the team using Engines and APU design and manufacturing experience.
• Work successfully in an Agile environment with local and global analysis teams.
• Create statements of work and review analysis output.
• Communicate effectively with manufacturing personnel, suppliers, customers, and Chief Engineers.
• Support Production, Supplier Transition/Reposition, and Value Engineering initiatives.
• Support Quality processes, including FAIR, RMRAs, and QNs.
• Perform drawing interpretation.
• Support supplier substantiation processes, including ESA, STICS, STR, FTR, and SCS.
• Support design change processes, including ECN, EMA, and Deviation Waiver.
• Support process transformation to reduce design and manufacturing costs and cycle time.

• Bachelor’s degree in Engineering.
• Minimum of 5+ years of experience in the field or a related area.
• Excellent written and oral communication skills to interact with engineering teams, other disciplines, and external supplier or customer parties

• Ability to prioritize and adjust to constantly changing assignment requests.
• System-level understanding of a gas turbine engine.
• Understanding of aerospace manufacturing processes and requirements, including casting, machining, welding, and heat treatment.
• Strong drawing interpretation skills, including GD&T.
• Knowledge of the gas turbine engine industry, specifically regarding how design requirements are communicated and maintained in production through the following processes:
• Quality processes, including inspection methodologies and FAIR and RMRA reviews 
• Supplier substantiation processes, including ESA, STICS, STR, FTR, and SCS documentation. 
• Design change processes, including ECNs and EMAs.
• Proven understanding and application of fatigue and finite element analysis.
• Capability to perform complex analyses and hand calculations of engine FanC components.
• Excellent written and oral communication skills to interact with engineering teams, other disciplines, and external supplier or customer parties.
• Experience with FEA using ANSYS or an equivalent tool.
• Experience with 3D modeling using CAD.
• Experience with GOM analysis using structured-light scanning of gas turbine engine FanC components.

• Do you have a bachelor’s degree in Engineering and a minimum of five years of industry experience?
• Do you have gas turbine engine industry experience?
• Do you have GD&T, CAD, and engineering analysis skills?
• Do you have an understanding of aerospace manufacturing processes and requirements, including casting, machining, welding, and heat treatment?
• Do you have excellent written and oral communication skills to interact with engineering teams, other disciplines, and external supplier or customer parties?

• Determine launch and lifecycle change requirements.
• Prepare and manage project plans and schedules for implementation.
• Identify and mitigate project risks under GxP guidelines.
• Contribute to cross-functional launch and lifecycle teams.
• Collaborate with stakeholders to achieve launch milestones.
• Collaborate with stakeholders to identify, analyze, and prepare products for obsolescence or phase-out.
• Identify requirements for product variants.
• Prepare product representations in SAP, including master data.
• Participate in strategic and special projects as needed.
• Strive for continuous optimization by proactively identifying and removing roadblocks and risks.

• Bachelor’s degree in Business, Engineering, or a related function.
• Three or more years of experience in Manufacturing Project Management, Supply Chain, or a related discipline.
• Working knowledge of SAP, the Design Control process, and Agile/Scaled Agile Framework concepts.
• Excellent English communication skills.
• Strong cross-functional collaboration skills.
• Willingness to challenge the status quo.
• Passion for driving change.

• Experience within the medical device industry.
• PMP certification.

• Audit existing preventive maintenance (PM) programs and historical work order data within the CMMS.
• Identify procedural gaps and opportunities to improve maintenance effectiveness.
• Cross-reference asset inventories with field equipment to verify asset accuracy and equipment tagging.
• Prepare detailed gap analysis reports and recommend improvements.

• Develop, revise, and standardize preventive maintenance job plans and procedures for critical facility systems, including:
• HVAC Systems (Air Handling Units, HEPA filtration, VAV systems)
• Laboratory Exhaust Systems (Chemical fume hoods, biosafety cabinet exhaust systems, exhaust stacks)
• Plant Utilities (Chillers, cooling towers, boilers, compressed air systems)
• High-Purity Water Systems (RODI purification and distribution systems)
• Create standardized maintenance templates for mechanical, electrical, and plumbing disciplines.
• Develop clear maintenance procedures that improve consistency and technician efficiency.

• Integrate safety requirements into maintenance procedures, including:
• Lockout/Tagout (LOTO)
• Job Hazard Analyses (JHA)
• Personal Protective Equipment (PPE)
• Ensure maintenance procedures comply with:
• Roche Engineering Standards
• Good Manufacturing Practices (GMP)
• Good Laboratory Practices (GLP)
• Good Documentation Practices (GDP)
• Include pass/fail criteria, calibration checkpoints, and required data collection parameters within PM procedures.

• Support CMMS updates and data migration activities.
• Prepare change requests and upload documentation for new PM procedures.
• Collaborate with Plant Engineering and maintenance personnel to capture field knowledge and improve maintenance documentation.
• Analyze maintenance trends and recommend reliability improvements.
• Support continuous improvement initiatives focused on asset reliability, equipment uptime, and regulatory compliance.

• Bachelor's degree in Mechanical Engineering, Electrical Engineering, Facilities Engineering, or a related technical discipline (or equivalent technical experience).
• 5+ years of experience in facilities engineering, reliability engineering, or maintenance operations within a regulated industry.
• Strong knowledge of:
• Commercial and industrial HVAC systems
• Chilled water plants
• Industrial exhaust systems
• High-purity water (RODI) systems
• Preventive maintenance best practices
• Experience utilizing enterprise CMMS systems (SAP preferred).
• Excellent technical writing skills with experience developing maintenance procedures and documentation.
• Strong analytical and problem-solving abilities.
• Excellent communication skills with the ability to work effectively with maintenance technicians, engineers, and cross-functional teams.

• Experience within biotechnology, pharmaceutical, healthcare, or semiconductor manufacturing environments.
• Experience performing preventive maintenance program audits and optimization.
• Familiarity with regulatory requirements for GMP, GLP, and GxP environments.
• Experience developing standardized maintenance documentation and engineering procedures.
• Knowledge of reliability-centered maintenance (RCM) principles.

• Perform a comprehensive Preventive Maintenance Gap Analysis.
• Develop standardized Preventive Maintenance templates.
• Deliver finalized Preventive Maintenance job plans for critical facility systems.
• Prepare CMMS change requests and documentation to support implementation of updated maintenance procedures.

• Document incoming and outgoing shipments accurately.
• Manage inventory and maintain accurate material records.
• Support gas, chemical, and slurry distribution equipment across multiple facilities.
• Install, troubleshoot, repair, and decommission gas and chemical delivery systems.
• Perform cylinder and drum change-outs for gas and chemical systems.
• Support preventive maintenance and equipment reliability programs.
• Write, edit, and follow operating and maintenance procedures.
• Perform chemical deliveries, material movement, and offloading activities.
• Operate forklifts and pallet jacks to move materials (forklift certification preferred).
• Support quality management, emergency preparedness, and safety initiatives.
• Maintain compliance with company procedures and promote a zero-incident safety culture.
• Participate in ongoing technical training and career development programs.

• Experience with gas, chemical, or slurry applications in semiconductor wafer fabrication.
• Knowledge of gas and chemical handling procedures and emergency response.
• Experience with inventory management and shipment documentation.
• Strong troubleshooting and mechanical aptitude.
• Ability to lift and move materials safely.
• Strong communication and teamwork skills.
• Ability to follow detailed procedures and safety protocols.

• Barcode scanning experience.
• Forklift experience or certification.
• Experience with pallet jacks and material handling equipment.
• Preventive maintenance and equipment repair experience.
• Semiconductor manufacturing or cleanroom experience.
• Experience supporting gas distribution, chemical delivery, or logistics operations.

• Assemble products according to specifications.
• Ensure quality control during assembly.
• Maintain production efficiency.
• Operate tools and machinery safely.
• Report issues to supervisors.

• High School Diploma or GED required.
• 0–5 years of experience.
• Strong problem-solving skills.
• Excellent communication abilities.
• Proficiency in industry tools and software.

• Previous manufacturing experience preferred.

• Design, scale, and deploy machine learning and NLP pipelines using approved enterprise platforms, primarily Dataiku and Azure ML Studio.
• Evaluate and deploy advanced AI solutions using the Claude Agent SDK or comparable approved SDKs for complex cross-system automation.
• Architect and mature the global AI Use-Case Backlog.
• Guide deployment of NLP and Large Language Models (LLMs) for automated sorting, risk grading, and categorization of quality data.
• Oversee conceptual data modeling and integration pipelines supporting enterprise analytics repositories such as Snowflake and AWS.
• Partner with development teams to translate complex datasets into enterprise business intelligence views.

• Serve as Product Owner and provide architectural oversight for quality insight platforms, dashboards, and automation frameworks.
• Establish repository management, version control, and collaborative code review practices using Git.
• Drive standardized automation workflows using Jira and Confluence to improve operational efficiency.

• Ensure AI models, automated scripts, and data pipelines comply with Computerized System Validation (CSV), GxP, US FDA (21 CFR Part 820), and ISO 13485 standards.
• Guide technical validation documentation supporting data integrity.
• Partner with Quality Site Heads, Business Leaders, and global cross-functional teams to resolve enterprise reporting challenges.
• Establish and mentor an Operations Quality Community of Practice focused on AI and data insights.
• Coach team members on AI, data strategy, and best practices.

• Deploy and maintain a scalable enterprise AI platform supporting multiple global use cases.
• Maintain over 95% alignment between automated AI insights and manual audit findings while meeting validation requirements.
• Reduce the time required to generate monthly and quarterly quality reports through automation.
• Drive high user adoption and measurable efficiency improvements across enterprise data products.

• Education: Bachelor's, Master's, or Ph.D. degree in: Data Science, Informatics, Data Analytics, Computer Science, or related technical field.
• 5–7+ years of experience developing and deploying: Machine learning algorithms, Complex data models, Automated software tools supporting enterprise decision-making.
• Enterprise AI & Machine Learning: Dataiku, Azure ML Studio, Natural Language Processing (NLP), Large Language Models (LLMs), Prompt Engineering.
• Programming & Data Modeling: Python, SQL.
• Developer & Collaboration Tools: Git, Jira, Confluence, Script Automation Environments.
• Agentic AI Frameworks: Claude Agent SDK or comparable enterprise-approved development kits.
• Cloud Data & Analytics Platforms: Snowflake, AWS, ThoughtSpot, Tableau.
• International business travel required based on project and strategic needs.

• Prior experience with Computerized System Validation (CSV) protocols.

• Design, develop, and maintain high-quality Flight Management System (FMS) software.
• Develop core software architecture and applications for next-generation avionics platforms.
• Integrate Flight Management software into new aerospace products.
• Collaborate with cross-functional engineering teams to define software requirements and technical specifications.
• Develop software solutions that meet performance, scalability, security, and certification requirements.
• Participate in software architecture, design reviews, and code reviews.
• Perform software testing, debugging, integration, and validation using laboratory test benches.
• Support functional software releases and certification activities.
• Stay current with emerging software technologies, avionics standards, and industry best practices.
• Contribute to Agile/Scrum development activities and continuous process improvements.

• Bachelor's degree in Computer Science, Software Engineering, Computer Engineering, Electrical Engineering, or another STEM-related discipline.
• Minimum 8 years of Flight Management System (FMS) software development experience.
• Strong C++ programming and object-oriented software development skills.
• Experience with Agile, Scrum, or similar software development methodologies.
• Strong software architecture and system design experience.
• Ability to work effectively within cross-functional engineering teams.
• Excellent analytical, problem-solving, and communication skills.

• Navigation Database Management
• Flight Planning
• Lateral and Vertical Guidance
• Performance & Trajectory Prediction
• Flight Performance Optimization
• Radio Tuning
• Approach Operations
• Datalink Systems
• Takeoff & Landing Functions
• Flight Deck User Interface Development
• Embedded Software Development
• Multi-core / Multi-threaded Software Development
• DO-178C Software Development Lifecycle
• Software Verification & Validation
• Object-Oriented Analysis & Design (OOAD)
• Advanced degree in Computer Science or related engineering discipline

• Work on cutting-edge aerospace technology that shapes the future of flight.
• Competitive weekly pay.
• Hybrid work schedule with flexibility.
• Opportunity to collaborate with world-class aerospace engineers.
• Gain experience developing advanced avionics systems for next-generation aircraft.
• Work on highly visible, technically challenging projects in a collaborative environment.
• Expand your expertise in safety-critical software development and certification.

• Act as the lead point of contact for day-to-day operations within the VPP Department and VPP Domain.
• Manage, track, and analyze cases from intake through resolution, ensuring timely follow-up and escalation.
• Partner with Application Management Support (AMS) on incident and problem management processes.
• Monitor operational workflows and identify process gaps, recommending improvements to increase efficiency and consistency.
• Analyze recurring field questions and issue trends to identify root causes and recommend process or training improvements.

• Serve as the subject matter expert (SME) and VPP contact for system enhancement projects, including StoneEagle Admin platform, Private Label, RouteOne, and SGI.
• Collaborate with technology, data, and business teams to ensure project requirements meet business needs.
• Assist with gathering, writing, and revising business user stories and system requirements.
• Manage Jira user stories, including writing, prioritization, and refinement.
• Configure product, plan, and pricing changes within the StoneEagle Admin system.
• Support VPP Product Operations and Product Development teams during requirements gathering and testing.
• Assist VPP Domain Product Owners with Jira backlog grooming and prioritization.
• Develop and execute test scenarios across multiple test environments.
• Manage the Secure Online Reporting (SOLR) invoice and billing process.
• Support weekly manual payment exception processing for downstream accounting systems.
• Provide support to the VPP Reinsurance Team with dealer wire transfers.

• Provide operational expertise during development and enhancement of VPP-related system applications.
• Create and maintain VPP system process maps and Standard Operating Procedures (SOPs).
• Utilize Kaizen and Toyota Business Practices (TBP) methodologies to develop and implement process improvements.

• Create, revise, and communicate training materials related to VPP technology projects.
• Create, revise, and post FSBs as requested.
• Support special VPP projects as assigned..

• Education: Bachelor's degree (BA or BS).
• Experience: 5–7+ years of relevant experience in technology operations, field support, operations management, or a similar industry.
• Working knowledge of technology products, operational processes, and workflows.
• Proficiency with Microsoft Office applications, including: Excel, PowerPoint, Visio, Word.
• Proficiency with Jira or similar case/workflow management tools.
• Strong business system configuration skills and experience supporting operational system processes.
• Excellent verbal and written communication skills.
• Strong organizational skills, attention to detail, and ability to manage multiple priorities.

• Self-starter with the ability to hit the ground running.
• Strong problem-solving skills.
• Excellent communication and stakeholder management skills.
• Proactive and initiative-taking mindset.
• Positive and optimistic approach.
• Project Management or Product Management experience (title not required).
• Operational supervision/management experience.
• Case management and investigation experience.
• Experience partnering with business domains, product owners, and cross-functional teams.
• Experience monitoring workflows and managing Jira or other ticketing platforms.
• Experience with MS Excel or Tableau.
• Experience with ticketing systems such as Jira, ServiceNow, or similar platforms.

• Agile Certification.
• Experience with Agile methodologies, initiative planning, and project launches.

• Perform preventative, predictive, and corrective maintenance on production and facility equipment.
• Troubleshoot, repair, and rebuild pumps, gear heads, reducers, motors, and mechanical drive systems.
• Install and repair piping systems including black iron, stainless steel, copper, PVC, and flexible tubing.
• Replace seals, bearings, O-rings, gaskets, belts, chains, sprockets, gears, rollers, sheaves, and related components.
• Perform welding and fabrication on stainless steel, carbon steel, aluminum, sheet metal, and Lexan guards.
• Operate plasma cutters, torches, machine shop equipment, and precision measuring tools.
• Wire and repair electric motors and perform basic electrical troubleshooting.
• Read electrical schematics and wiring diagrams while ensuring compliance with the National Electrical Code (NEC).
• Troubleshoot and repair high-speed filling, packaging, conveying, bottling, capping, and seaming equipment.
• Maintain proper operation of electrical and mechanical devices including switches, push buttons, timers, solenoids, AC/DC motors, disconnects, barcode scanners, and industrial printers.
• Respond quickly to equipment failures and production stoppages to minimize downtime.
• Perform machine adjustments and support continuous improvement initiatives.
• Complete assigned preventative maintenance schedules and maintain accurate maintenance documentation.
• Maintain inventory of spare parts, tools, and repair materials.
• Assist outside contractors during equipment repairs and installations.
• Maintain housekeeping standards within the maintenance shop.
• Follow all applicable FDA GMP, USDA, OSHA, and company safety regulations.

• Technical degree or equivalent technical training.
• Minimum of 2 years of industrial maintenance experience.
• Strong experience troubleshooting mechanical and electrical systems.
• Experience working with high-speed manufacturing equipment.
• Robotics maintenance experience.
• Ability to read electrical schematics and wiring diagrams.
• Experience with welding, fabrication, machine repair, pumps, motors, conveyors, and industrial maintenance practices.
• Strong troubleshooting and problem-solving skills.
• Ability to work independently and as part of a maintenance team.
• Willingness to work overtime, weekends, or extended hours as business needs require.
• Stable employment history demonstrating reliability and longevity.

• Experience in a manufacturing or cleanroom environment.
• Experience with preventative and predictive maintenance programs.

• Design, implement, and maintain the IBM ELM/Jazz platform for aerospace engineering workflows.
• Serve as a technical focal point for IBM DOORS Next Generation, Engineering Workflow Management, Engineering Test Management, Rhapsody, Global Configuration Management, and Jazz Team Server.
• Configure project areas, permissions, access controls, workflows, templates, and lifecycle processes.
• Integrate IBM ELM with PLM, CAD, ERP, MES, and other enterprise engineering systems.
• Develop linked data integrations using OSLC, REST APIs, middleware, and integration adapters.
• Define data federation and synchronization strategies that support a reliable single source of truth.
• Establish configuration management links between systems engineering data and product structures, including as-designed and as-built bills of materials.
• Align systems engineering workflows with ARP4754 aerospace development guidelines.
• Track Development Assurance Levels across system architecture elements.
• Develop automated traceability matrices, verification reports, and compliance documentation.
• Support compliance activities involving ARP4754, DO-178C, and DO-254.
• Partner with Quality Assurance teams to align Engineering Test Management with Requirements-Based Engineering workflows.
• Manage change requests, defect tracking, and planning activities within Engineering Workflow Management.
• Troubleshoot platform performance, configuration conflicts, availability, and system integration issues.
• Develop automation scripts, plugins, and integrations using JavaScript, Python, REST APIs, and OSLC.
• Create automated reports, enterprise dashboards, and compliance visualizations using IBM reporting tools, Power BI, Tableau, BIRT, or similar platforms.
• Collaborate with engineering, quality, software, hardware, manufacturing, and enterprise technology teams.

• Minimum of 5 years of experience supporting software or systems engineering tools.
• Deep hands-on experience with the IBM Engineering Lifecycle Management ecosystem.
• Experience with IBM DOORS Next Generation, Engineering Workflow Management, and Engineering Test Management.
• Experience supporting Requirements-Based Engineering within aerospace applications.
• Proven experience integrating IBM ELM with enterprise engineering and product lifecycle systems.
• Experience using OSLC, REST APIs, middleware, or integration adapters.
• Experience with Requirements-Based Engineering and Model-Based Systems Engineering.
• Strong practical knowledge of ARP4754 aerospace development frameworks.
• Familiarity with DO-178C software assurance and DO-254 hardware assurance requirements.
• Experience administering engineering workflows, access controls, permissions, and configuration management.
• Experience developing dashboards, automated reports, and compliance metrics.
• Scripting or automation experience using JavaScript, Python, or related technologies.
• Strong documentation, communication, and stakeholder management skills.
• Ability to work effectively across engineering and enterprise technology teams.

• Bachelor’s or Master’s degree in Aerospace Engineering, Systems Engineering, Computer Science, or a related technical field required.

• Experience integrating IBM ELM with Siemens Teamcenter, PTC Windchill, Dassault 3DEXPERIENCE, CAMEO, or similar enterprise platforms.
• Experience with IBM Rhapsody, Global Configuration Management, Jazz Team Server, and Engineering Lifecycle Optimization tools.
• Experience creating dashboards using Power BI, Tableau, BIRT, or IBM reporting solutions.
• IBM ELM certification or related IBM credentials.
• Experience supporting Digital Thread initiatives.
• Familiarity with Agile, SAFe, and Waterfall delivery methodologies.
• Experience supporting safety-critical aerospace systems and certification activities.
• Strong knowledge of systems engineering lifecycle management and regulatory traceability.

• Clean and sanitize shoe scrubber stations throughout the facility.
• Apply granulated sanitizer according to established procedures.
• Ensure assigned areas are properly cleaned using approved cleaning and sanitizing processes.
• Clean and sanitize processing equipment, production equipment, and designated plant areas according to established job standards.
• Clean and sanitize food-processing equipment and food-processing facilities.
• Operate specialized cleaning equipment, including automatic floor scrubbers, vacuums, and scissor lifts.
• Prevent cross-contamination of products, work-in-progress materials, food-contact surfaces, and food-contact packaging during sanitation activities.
• Follow all company sanitation Standard Operating Procedures.
• Remove trash and garbage from designated areas throughout the facility.
• Mop floors and clean floor drains, exterior areas, and other areas requiring attention.
• Complete all required sanitation records, work orders, and related documentation accurately and on time.
• Wash, sanitize, and maintain cleaning carts, tools, and equipment.
• Maintain sanitation-related equipment, including automatic floor scrubbers, vacuums, cleaning tools, and other assigned equipment.
• Keep cleaning supplies stocked, organized, and readily available.
• Report damaged equipment, safety concerns, or sanitation issues to the appropriate supervisor.
• Work in other departments or areas as needed, provided proper training has been completed.
• Perform additional duties as assigned by the Sanitation Supervisor.
• Follow all applicable FDA, OSHA, company, and facility policies and procedures.

• High school diploma or GED.
• Ability to follow written and verbal instructions.
• Ability to complete sanitation and work-order documentation accurately.
• Ability to work safely around cleaning chemicals, food-processing equipment, and production machinery.
• Ability to work a rotating 12-hour schedule, including weekends and holidays as required.
• Ability to stand, walk, bend, reach, push, pull, and perform repetitive cleaning tasks for extended periods.
• Ability to work independently and as part of a team.

• Previous sanitation, janitorial, housekeeping, or industrial cleaning experience.
• Experience working in a food-processing, manufacturing, or regulated production environment.
• Knowledge of Good Manufacturing Practices.
• Experience operating floor scrubbers, vacuums, scissor lifts, or similar sanitation equipment.
• Familiarity with FDA, OSHA, food-safety, or quality-system requirements.

• Monday: 12 hours
• Tuesday: 12 hours
• Wednesday: Off
• Thursday: Off
• Friday: 12 hours
• Saturday: 12 hours
• Sunday: 12 hours

• Monday: Off
• Tuesday: Off
• Wednesday: 12 hours
• Thursday: 12 hours
• Friday: Off
• Saturday: Off
• Sunday: Off

•  Assemble mechanical, electrical, and electronic components using hand and power tools. 
•  Perform product testing, calibration, and verification to ensure quality and accuracy. 
•  Inspect components and finished products to meet FDA, ISO, and company standards. 
•  Troubleshoot production issues and work with Engineering and Quality teams to resolve them. 
•  Complete production documentation, material tracking, and non-conformance reports. 
•  Follow SOPs, cGMPs, QMS, and all safety procedures. 
•  Assist in training team members as needed. 
•  Support continuous improvement initiatives and perform other assigned duties. 

•  High School Diploma or GED required. 
•  Manufacturing or assembly experience preferred. 
•  Ability to read and interpret technical drawings and work instructions. 
•  Experience using hand and power tools. 
•  Basic computer and math skills. 
•  Strong mechanical aptitude and hand-eye coordination. 
•  Ability to lift 50 pounds or more. 
•  Strong English communication skills (reading, writing, and speaking). 

•  Experience in FDA or ISO regulated manufacturing environments. 
•  Knowledge of cGMP and Quality Management Systems (QMS). 
•  Experience with testing, calibration, or inspection processes.

• Lead and coordinate Integrated Supply Chain projects within the Aerospace business.
• Monitor project performance, identify risks, and develop effective corrective actions to ensure successful project outcomes.
• Create and maintain Line of Balance, Clear to Build, and related planning reports and tools.
• Use SAP to analyze supply chain data, track project milestones, and support operational decision-making.
• Develop project-tracking mechanisms, metrics, and dashboards to measure performance and progress.
• Collaborate with Supply Chain, Operations, Planning, Procurement, Engineering, and Manufacturing stakeholders.
• Drive continuous improvement initiatives focused on productivity, delivery, quality, and customer satisfaction.
• Prepare and present project updates, performance reports, and recommendations to leadership.
• Support problem-solving activities and facilitate cross-functional alignment to resolve operational challenges.

• Bachelor’s degree in supply chain, Business, Operations, Engineering, or a related field; equivalent experience will be considered.
• At least 7 years of experience in Supply Chain, Operations, Project Management, or a related discipline.
• Strong SAP experience with the ability to analyze and manage supply chain data.
• Experience creating and managing Line of Balance and Clear to Build reports.
• Advanced Microsoft Excel skills, including PivotTables, VLOOKUP/XLOOKUP and Data analysis and reporting.
• Proven ability to manage multiple projects and priorities in a fast-paced environment.
• Strong communication, analytical, and problem-solving skills.

• Aerospace or manufacturing industry experience.
• Experience leading cross-functional project teams.
• Knowledge of Integrated Supply Chain processes and operational metrics.
• Continuous improvement, Lean, or Six Sigma experience.

• Perform packaging operations according to established production procedures and work instructions.
• Support manufacturing operations while ensuring products meet quality and production standards.
• Transport chemicals, raw materials, and equipment using pumps, piping systems, forklifts, pallet jacks, and dollies.
• Verify product quality and quantity throughout the manufacturing process.
• Clean equipment and work areas following production activities.
• Coordinate proper disposal of waste materials and complete required compliance documentation.

• Maintain accurate batch records and production documentation.
• Complete equipment logbooks and required production records.
• Communicate production status, equipment conditions, and process deviations to supervisors.
• Ensure all in-process equipment and containers are properly labeled.
• Follow quality guidelines and manufacturing procedures at all times.

• Follow all production procedures, safety policies, and environmental regulations.
• Wear appropriate personal protective equipment (PPE), including respirators, gloves, and protective suits as required.
• Identify and report unsafe conditions and assist in resolving safety concerns.
• Participate in required safety, quality, and operational training.
• Maintain a clean, organized, and safe work environment.

• High school diploma or equivalent with 1–3 years of manufacturing experience, or an Associate degree in a Life Sciences discipline with 1–2 years of related experience.
• Forklift experience is required.
• Strong mechanical aptitude and troubleshooting skills.
• Basic computer skills.
• Ability to safely handle chemicals while following established safety procedures.
• Strong written and verbal communication skills.
• Excellent organizational and interpersonal skills.
• Ability to accurately complete production documentation.
• Ability to lift materials, perform repetitive tasks, and work safely in a manufacturing environment.

• 1–2 years of chemical manufacturing experience preferred.
• Experience working in chemical, pharmaceutical, or industrial manufacturing environments.
• Experience operating pallet jacks, pumps, piping systems, and other material handling equipment.
• Knowledge of manufacturing quality systems and production documentation.

• Packaging Operations
• Chemical Manufacturing
• Forklift Operation
• Manufacturing
• Production Operations
• Safe Chemical Handling
• Mechanical Aptitude
• Troubleshooting
• GMP / Safety Compliance
• Production Documentation

• 30-minute onsite interview

Senior Integrated Supply Chain Project Specialist

• Lead and coordinate Integrated Supply Chain (ISC) projects supporting aerospace operations.
• Monitor project performance, identify risks, and implement corrective actions to ensure successful project execution.
• Create and maintain Line of Balance (LOB) and Clear To Build reports.
• Utilize SAP to analyze supply chain data and support operational decision-making.
• Develop project dashboards, metrics, and reporting tools to track project performance.
• Collaborate with Supply Chain, Operations, Planning, Procurement, Engineering, and Manufacturing teams.
• Drive continuous improvement initiatives focused on productivity, quality, delivery, and customer satisfaction.
• Prepare and present project updates, performance metrics, and recommendations to leadership.
• Support cross-functional problem-solving and operational improvement initiatives.
• Manage multiple projects while ensuring schedules, priorities, and deliverables are achieved.

• Bachelor's degree in Supply Chain, Business, Operations, Engineering, or a related field; equivalent experience considered.
• Minimum of 7 years of experience in Supply Chain, Operations, Project Management, or a related discipline.
• Strong SAP experience with the ability to analyze and manage supply chain data.
• Experience creating and maintaining Line of Balance (LOB) and Clear To Build reports.
• Advanced Microsoft Excel skills, including Pivot Tables, VLOOKUP/XLOOKUP, data analysis, and reporting.
• Proven ability to manage multiple projects in a fast-paced environment.
• Strong analytical, organizational, communication, and problem-solving skills.

• Bachelor's degree in Supply Chain, Business, Operations, Engineering, or a related field required (or equivalent experience).

• Aerospace or manufacturing industry experience.
• Experience leading cross-functional project teams.
• Knowledge of Integrated Supply Chain (ISC) processes and operational metrics.
• Lean Manufacturing or Six Sigma experience.
• Experience developing dashboards, KPIs, and operational reporting.
• Strong continuous improvement mindset.

• Perform packaging operations in accordance with approved manufacturing procedures and production protocols.
• Transport chemicals, raw materials, and equipment using forklifts, pallet jacks, pumps, piping systems, and dollies.
• Monitor production processes to ensure product quality, accuracy, and efficiency.
• Complete batch records, production logs, and compliance documentation accurately.
• Verify product quality and quantities throughout the manufacturing process.
• Maintain accurate equipment status and communicate production updates to supervisors.
• Clean production equipment and work areas following production activities.
• Properly dispose of waste materials in accordance with environmental and safety procedures.
• Wear and maintain required personal protective equipment (PPE), including respirators, gloves, and protective suits as required.
• Label in-process equipment and containers according to company procedures.
• Follow all safety policies, quality standards, and manufacturing procedures.
• Participate in required safety training, quality initiatives, and continuous improvement efforts.
• Maintain a clean, organized, and safe production environment.

• High school diploma or equivalent with 1–3 years of manufacturing or industrial production experience, or an Associate degree in a Life Science field with 1–2 years of related experience.
• Forklift operating experience is required.
• Strong communication skills, both written and verbal.
• Basic computer skills for production documentation and recordkeeping.
• Mechanical aptitude and troubleshooting abilities.
• Strong organizational and interpersonal skills.
• Ability to safely handle chemicals while following established safety procedures.
• Ability to work rotating 12-hour day and night shifts.
• Ability to wear required PPE for extended periods.

• 1–2 years of chemical manufacturing experience.
• Experience working in industrial, chemical, pharmaceutical, or process manufacturing environments.
• Experience operating pumps, piping systems, or material handling equipment.
• Experience maintaining batch records and production documentation.
• Knowledge of chemical handling procedures and manufacturing safety practices.

• Competitive weekly pay.
• Stable 6-month contract with the possibility of extension.
• Opportunity to build valuable skills in chemical manufacturing and industrial production.
• Work in a safety-focused environment with advanced manufacturing equipment.
• Gain experience with forklift operation, production systems, and regulated manufacturing processes.
• Join a collaborative team committed to quality, safety, and continuous improvement.

• Location: Altavista, VA 24517
• Schedule: 12-hour overnight shift
• Shift Hours: 6:00 PM – 6:30 AM
• Employment Type: W2 3 Months Contract
• Overtime: Hours worked over 40 per week are paid at time-and-a-half.
• Pay Rate: $14.00 - $15.55.

• Inspect raw materials and finished products for quality and accuracy.
• Label and package products according to established procedures.
• Maintain production records and documentation in accordance with Good Manufacturing Practices (GMP).
• Follow standard operating procedures and quality guidelines.
• Work effectively in a clean-room environment when required.
• Ensure products meet quality standards before shipment.
• Maintain a clean, organized, and safe work area.
• Perform other production-related duties as assigned under moderate supervision.

• Previous manufacturing, production, packaging, or warehouse experience preferred.
• Ability to work in a regulated manufacturing or clean-room environment.
• Strong attention to detail and commitment to quality.
• Ability to follow written procedures and work instructions.
• Comfortable standing, walking, and performing repetitive tasks for extended periods.
• Reliable attendance and ability to work a 12-hour overnight shift.
• Ability to work independently with moderate supervision.

• Location: Altavista, VA 24517
• Schedule: 12-hour overnight shift
• Shift Hours: 6:00 PM – 6:30 AM
• Employment Type: Full-Time Contract
• Overtime: Hours worked over 40 per week are paid at time-and-a-half.
• Pay Rate: $14 - $15.55.

• Dental insurance
• Health insurance
• Life insurance
• Vision insurance

• High school or equivalent (Required)

• Overnight Shift (Required)

• Altavista, VA 24517 (Required)

•  Support day-to-day Sales Operations activities to ensure efficient and accurate business processes. 
•  Process and analyze sales transactions while maintaining data integrity. 
•  Monitor inventory levels and perform inventory analysis. 
•  Support the Order-to-Cash (O2C) process by ensuring timely and accurate transaction processing. 
•  Maintain accurate records and ensure compliance with company policies and procedures. 

•  Investigate, reconcile, and resolve discrepancies related to sales orders, inventory, and financial transactions. 
•  Prepare account and transaction reconciliations while identifying root causes of variances. 
•  Ensure data accuracy and integrity across multiple business systems. 
•  Support internal controls and operational compliance initiatives. 

•  Develop reports, dashboards, and presentations using Microsoft Excel and PowerPoint. 
•  Analyze operational and sales data to identify trends and recommend process improvements. 
•  Maintain and update information within the JD Edwards (JDE) ERP system. 
•  Support reporting requests and special projects as assigned. 

•  Collaborate with Sales, Finance, Customer Service, Supply Chain, and other cross-functional teams to resolve operational issues. 
•  Clearly communicate findings and recommendations to stakeholders. 
•  Participate in continuous improvement initiatives that enhance operational efficiency and data accuracy. 

•  Associate or Bachelor's degree in Business Administration, Finance, Supply Chain, Operations, Accounting, Data Analytics, or a related field. 
• 1–2 years of experience as a Data Analyst, Sales Operations Analyst, Business Analyst, or in a related analytical role.
•  Advanced proficiency in Microsoft Excel, including: 
  •  Pivot Tables 
  •  VLOOKUP/XLOOKUP 
  •  INDEX/MATCH 
  •  Advanced formulas 
  •  Data analysis and reporting 
•  Strong proficiency in Microsoft PowerPoint for creating executive-level presentations. 
•  Experience using JD Edwards (JDE) or a similar ERP system. 
•  Knowledge of Order-to-Cash (O2C) business processes. 
•  Experience performing reconciliations and resolving transaction discrepancies. 
•  Strong analytical and problem-solving skills. 
•  Excellent organizational skills with exceptional attention to detail. 
•  Ability to prioritize multiple tasks and meet deadlines in a fast-paced environment. 
•  Strong written and verbal communication skills. 

•  Experience supporting Sales Operations, Customer Service, Finance, or Supply Chain functions. 
•  Experience with inventory management and sales reporting. 
•  Continuous improvement mindset with the ability to identify opportunities to streamline business processes. 
•  Advanced reporting and data analysis experience. 

•  Sales Operations 
•  Data Analysis 
•  Microsoft Excel (Advanced) 
•  JD Edwards (JDE) 
•  Order-to-Cash (O2C) 
•  Financial Reconciliations 
•  Inventory Analysis 
•  Microsoft PowerPoint 
•  ERP Systems 
•  Process Improvement 

•  Procure raw materials, components, supplies, and services to support manufacturing operations. 
•  Source suppliers, obtain quotations, negotiate pricing, terms, and delivery schedules, and manage supplier relationships. 
•  Issue purchase orders and ensure timely delivery of materials. 
•  Plan, schedule, and coordinate the movement of raw materials, components, and finished goods. 
•  Monitor inventory levels and maintain material availability to support production schedules. 
•  Coordinate supplier deliveries and resolve material shortages or delivery issues. 
•  Maintain accurate purchasing, inventory, and planning data within ERP systems. 
•  Assist with logistics planning and material handling activities. 
•  Collaborate with manufacturing, logistics, quality, and engineering teams to support production requirements. 
•  Support supply chain planning initiatives by following established procedures and best practices. 
•  Analyze inventory, demand, and supplier performance to identify opportunities for process improvements. 
•  Contribute to continuous improvement initiatives that increase supply chain efficiency and operational performance. 
•  Ensure the quality, accuracy, and timeliness of procurement and planning activities. 
•  Perform a variety of non-routine assignments while exercising sound judgment and working independently.

•  Bachelor's degree required. 
• 3–5 years of professional experience with a Bachelor's degree OR a Master's degree with relevant experience.
•  Experience in procurement, purchasing, supply chain, materials planning, inventory management, logistics, manufacturing, or a related field. 
•  Experience sourcing suppliers and negotiating vendor contracts. 
•  Strong organizational, analytical, and problem-solving skills. 
•  Ability to independently manage multiple priorities while following established procedures. 
•  Excellent communication and collaboration skills. 
•  Proficiency with Microsoft Office, particularly Excel. 

•  Experience using SAP ERP or similar ERP systems. 
•  Experience supporting manufacturing or production environments. 
•  Knowledge of inventory control, demand planning, material planning, and supply chain processes. 
•  Experience coordinating supplier performance and production schedules.

• Conduct and review internal audits in accordance with the Internal Audit Schedule.
• Lead the development and scheduling of regional internal audits and support audit response activities.
• Provide regulatory compliance expertise by assessing gaps identified through the EMEA LOC/DC Inspection Readiness Program.
• Identify, assess, and communicate proactive compliance risks ("Find It, Fix It") to regional leadership to support preventative compliance initiatives.
• Partner with Regulatory Affairs, Quality, Commercial, and Supply Chain teams to support compliant product distribution and lifecycle activities.
• Escalate emerging compliance issues, risks, and trends to management through data analysis and reporting.
• Manage regional LOC licenses across the EMEA region.
• Collaborate closely with the regional Regulatory Compliance team to support regional compliance objectives.

• Education: Bachelor's degree in Regulatory Affairs, Quality, Engineering, Life Sciences, or a related discipline.
• Experience: 6–8 years of progressive experience in Regulatory Compliance, Quality, or a related function within a regulated industry.
• Strong experience serving as a Lead Internal Auditor.
• Strong knowledge of regulatory and compliance requirements across EMEA markets.
• Experience supporting audits, inspections, and leading compliance assessments.
• Ability to manage complex compliance initiatives involving multiple countries and cross-functional stakeholders.
• English language proficiency required.
• Ability to travel moderately throughout the EMEA region (Europe, Middle East, and Africa).

• Advanced degree in a scientific, regulatory, or business-related field.
• Auditing experience within the medical device or healthcare industry.
• Familiarity with EMEA regulatory authorities and compliance frameworks.
• Experience working within a global or matrixed organization.
• Exposure to regulatory inspections involving multi-country operations.
• Quality or Regulatory certifications (e.g., RAC, ASQ).
• Strong analytical, risk management, and problem-solving skills.
• Excellent written and verbal communication skills.
• Additional European languages preferred.
• Quality or Regulatory certifications preferred but not required.

Mechanical Design Engineer

• Design, develop, and analyze static gas turbine engine and APU structural components.
• Perform structural, stress, vibration, and heat transfer analyses for aerospace components.
• Develop mechanical designs that meet customer, regulatory, and program requirements.
• Lead engineering activities for component design, analysis, and product development.
• Conduct engineering design reviews and present technical findings to internal and external stakeholders.
• Collaborate with project engineering teams to support program execution and technical objectives.
• Develop and maintain engineering documentation, reports, calculations, and design records.
• Support resource planning, workload coordination, and technical leadership within the engineering team.
• Ensure compliance with engineering standards, processes, and quality requirements.
• Drive continuous improvement initiatives and engineering best practices.
• Provide technical guidance and mentorship to junior engineers as needed.

• Bachelor's degree in Mechanical Engineering or a related engineering discipline.
• Minimum of 8 years of mechanical design and engineering experience.
• Experience designing and analyzing aerospace mechanical components.
• Strong background in structural, stress, vibration, and heat transfer analysis.
• Experience with gas turbine engines, propulsion systems, or Auxiliary Power Units (APUs).
• Knowledge of engineering design standards, manufacturing processes, and product development.
• Ability to lead technical projects and coordinate cross-functional engineering activities.
• Strong written and verbal communication skills.
• Excellent analytical, problem-solving, and organizational abilities.

• Bachelor's degree in Mechanical Engineering or a related engineering discipline required.

• Aerospace or Aviation and Aerospace Component Manufacturing experience.
• Experience supporting engine structures or propulsion system development.
• Experience leading engineering design reviews.
• Familiarity with finite element analysis (FEA) and structural analysis tools.
• Experience with engineering documentation and configuration management.
• Previous technical leadership or project engineering experience.

• Work under the direction of Analytical Scientists to quantify lipid nanoparticles (LNPs) encapsulating nucleic acids.
• Analyze raw materials used in LNP formulations.
• Establish relationships between the physicochemical characteristics of experimental nanoparticle formulations and their efficacy and safety.
• Maintain detailed records of analytical data.
• Interface directly with other functional teams.
• Share responsibility for basic laboratory management activities, including supply ordering, instrument calibration, and schedule maintenance.

• Master’s or bachelor’s degree in pharmaceutical sciences, bioengineering, chemical engineering, chemistry, or a related scientific discipline.
• At least two years of experience; an equivalent combination of education and experience may be considered.
• Proficiency in formulating buffers.
• Excellent attention to detail and the ability to produce consistent results and communicate them effectively to the team.
• Ability to work as a team player, multitask, manage multiple projects simultaneously, and excel in a collaborative work environment.
• Proficiency in Microsoft Excel.
• Excellent oral and written communication skills.

• Practical experience with analytical methods such as RiboGreen, Dynamic Light Scattering (DLS), and zeta potential measurement.
• Previous experience with High-Performance Liquid Chromatography (HPLC).
• Experience and proficiency with other analytical techniques.
• Previous experience with advanced analytical software, including Prism or JMP.

• Receive, inspect, document, store, and return gas cylinders and chemical ampoules.
• Manage inventory levels and coordinate the ordering of materials from multiple vendors.
• Track and trend site gas and chemical usage.
• Prepare weekly, monthly, and quarterly inventory and usage reports for management.
• Accurately document shipments, deliveries, material movements, and inventory transactions.
• Use barcode systems to receive, track, and manage materials.
• Support chemical deliveries, chemical storage activities, and material offloading.
• Move gas cylinders, chemical ampoules, drums, and other materials using pallet jacks and forklifts.
• Perform gas cylinder, chemical drum, and ampoule changes on applicable delivery systems.
• Support the technical requirements of gas, chemical, and slurry distribution equipment.
• Provide technical support and problem resolution for more than 2,000 pieces of distribution equipment from various manufacturers.
• Install, commission, decommission, troubleshoot, repair, and maintain gas and chemical systems.
• Perform preventive maintenance and sustaining-operation activities.
• Support project-related equipment installations, upgrades, and operational improvements.
• Troubleshoot complex equipment issues and implement appropriate corrective actions.
• Write, edit, review, and execute operating and maintenance procedures using Microsoft Word and Excel.
• Support emergency preparedness and respond appropriately to gas or chemical incidents.
• Follow all applicable safety, quality, environmental, and regulatory requirements.
• Promote a zero-incident culture focused on safety, quality, and operational excellence.
• Support inventory-management business objectives, budgets, and continuous-improvement initiatives.
• Participate in comprehensive on-the-job technical training and qualification programs.
• Assist with employee training and serve as a subject-matter expert for gas, chemical, or slurry equipment.

• EMD Electronics gas systems
• Applied Energy Systems gas systems
• Fuji liquid delivery systems
• Air Liquide gas and chemical systems
• Gas, chemical, and slurry distribution equipment from various manufacturers

• Demonstrated knowledge of gas or chemical applications within a semiconductor wafer fabrication environment.
• Knowledge of gas and chemical safety practices, emergency response, and hazardous-material handling.
• Experience documenting shipments and inventory activities.
• Experience managing inventory levels and material-ordering processes.
• Strong Microsoft Office skills, particularly Microsoft Excel and Word.
• Ability to accurately prepare reports and maintain inventory records.
• Ability to read, write, edit, and follow operating and maintenance procedures.
• Ability to safely use material-handling equipment, including pallet jacks.
• Ability to work independently and resolve technical or inventory-related issues.
• Strong attention to detail and commitment to quality and safety procedures.
• Ability to complete required technical training and qualification programs.

• Previous experience with gas, chemical, or slurry delivery equipment.
• Experience in semiconductor, wafer fabrication, cleanroom, or high-technology manufacturing operations.
• Barcode scanning or barcode-based inventory-management experience.
• Forklift operating experience.
• Current or previous forklift certification.
• Experience performing gas cylinder, chemical drum, or ampoule changes.
• Experience troubleshooting and maintaining gas or chemical distribution systems.

• Ability to lift and move gas cylinders, chemical ampoules, and materials weighing more than 50 pounds.
• Ability to push, pull, position, and secure gas cylinders and chemical containers.
• Ability to operate pallet jacks and occasionally operate a forklift.
• Ability to perform physical material-handling and equipment-maintenance activities throughout the shift.
• Ability to wear required personal protective equipment and comply with site safety procedures.

• Participate in the operation of filling, labeling, and packaging equipment of varying complexity in accordance with Production Manufacturing Records, applicable SOPs, ISO standards, and cGMP requirements.
• Perform aseptic gowning and filling tasks within the aseptic environment when participating in Filling Operations.
• Perform in-process quality checks for specific quality attributes, including Fill Check, Torque Check, Vision System Check, Label Alignment Check, and other required inspections.
• Inspect products for defects and verify conformance to quality standards, SOPs, ISO requirements, and cGMP regulations.
• Complete production documentation (Production Manufacturing Records) and associated SAP transactions, including lot numbers, expiration dates, intermediates, reconciliations, and related records.
• Visually inspect products for defects and compliance with quality standards.
• Clean work areas and decontaminate work surfaces according to defined procedures.
• Perform duties in accordance with SOPs, Quality System Regulations (QSRs), safety requirements, and regulatory standards.
• Perform scheduled environmental monitoring activities in Filling Suites as required.
• Perform warehousing activities as needed, including: Fill preparation, Picking, Issuing, Returns, Internal distribution of goods, Receiving, Shipping, Lift up to 50 pounds.
• Perform other duties as assigned by management.

• Education: High School Diploma or GED.
• Experience: 1–2 years of previous experience in:
• Operations/Production environment
• Filling operations
• Labeling operations
• Warehouse operations
• Or an equivalent combination of education and experience.
• Equivalent combination of education and work experience accepted.
• Previous experience in a GMP-regulated environment.

• Format: One 1-hour onsite interview.
• Interview Includes: A tour of the production lines so candidates can see exactly what the position entails.
• Interview Schedule: Interviews will be conducted during the 2nd Shift (3:00 PM – 11:30 PM). No interviews will be scheduled earlier in the day.

• Operate filling, labeling, and packaging equipment according to Production Manufacturing Records (PMRs), Standard Operating Procedures (SOPs), and cGMP requirements.
• Package, label, inspect, and prepare finished products for distribution.
• Perform product inspections to ensure compliance with quality standards.
• Conduct in-process quality checks including fill verification, torque checks, vision system verification, and label alignment inspections.

• Complete Production Manufacturing Records and required SAP transactions accurately.
• Verify lot numbers, expiration dates, component reconciliation, and production documentation.
• Maintain compliance with ISO standards, cGMPs, and regulatory requirements.
• Assist with document review for completeness and accuracy.

• Perform aseptic gowning and filling operations as required.
• Support environmental monitoring activities within filling suites when assigned.
• Assist with warehouse operations, including receiving, picking, issuing materials, returns, internal distribution, and shipping activities.

• Clean and sanitize work areas following established procedures.
• Follow all safety policies and manufacturing guidelines.
• Maintain an organized and compliant production environment.
• Perform additional duties as assigned by management.

• High School Diploma or equivalent.
• 1–2 years of experience in manufacturing, production, warehouse, or related operations (or an equivalent combination of education and experience).
• Ability to follow detailed work instructions and SOPs.
• Comfortable performing repetitive production tasks while standing or remaining in the same work area throughout the shift.
• Ability to lift up to 50 pounds.
• Good communication and teamwork skills.
• Strong attention to detail and commitment to quality.

• Experience in pharmaceutical, medical device, or GMP-regulated manufacturing.
• Previous experience with filling, labeling, packaging, or warehouse operations.
• Mechanical aptitude.
• Basic math and computer skills.
• Good handwriting/documentation skills.
• Willingness to learn and train into more advanced manufacturing roles.

• Production Manufacturing
• Packaging
• Labeling
• Quality Inspection
• cGMP
• SAP Documentation
• Aseptic Manufacturing
• Manufacturing Operations
• Attention to Detail
• Teamwork

• One-hour onsite interview
• Includes a tour of the production area so candidates can see the work environment and daily responsibilities.
• Candidates should be comfortable working on a production line, following a structured schedule, and performing repetitive tasks throughout the shift.

Pharmaceutical Manufacturing Technician

• Operate as a primary or secondary operator for cGMP production of APIs and intermediates.
• Follow batch records, standard operating procedures (SOPs), and manufacturing documentation accurately.
• Operate, clean, and perform basic maintenance on production equipment.
• Maintain production areas and equipment in a safe, clean, and compliant condition.
• Follow proper potent compound handling techniques and all required PPE protocols.
• Communicate production status effectively during shift handoffs.
• Identify and resolve safety and process issues through routine inspections and audits.
• Support a team-based, multi-shift manufacturing environment.
• Complete additional production-related tasks as assigned by department leadership.
• Maintain accurate production documentation in accordance with cGMP requirements.

• Associate degree in Chemistry, Biochemistry, Chemical Engineering, or another Life Science discipline OR High School Diploma/GED with relevant work experience.
• Minimum of 2 years of pharmaceutical, chemical, or related manufacturing experience.
• Experience working in a cGMP-regulated manufacturing environment.
• Ability to read and follow written procedures and batch records.
• Basic computer skills including Microsoft Word, PowerPoint, and email.
• Strong written and verbal communication skills.
• Mechanical aptitude and the ability to operate production equipment and hand tools.
• Basic mathematical and measuring skills.
• Strong attention to detail with the ability to multitask.
• Ability to stand for extended periods and lift up to 50 pounds with assistance when necessary.
• Willingness to work with highly potent and hazardous materials while wearing required PPE, including respirators, lab coats, work uniforms, disposable coveralls, and other protective equipment.

• Associate degree in Chemistry, Biochemistry, Chemical Engineering, or a related Life Science field preferred.
• High School Diploma or GED with qualifying manufacturing experience will also be considered.

• Experience manufacturing pharmaceutical APIs or intermediates.
• Experience in chemical processing or regulated production environments.
• Familiarity with cGMP documentation and compliance.
• Strong safety mindset and experience working with hazardous materials.
• Experience operating production equipment in pharmaceutical manufacturing.

• Inspect raw materials and finished products for quality and accuracy.
• Label and package products according to established procedures.
• Maintain production records in compliance with Good Manufacturing Practices (GMP).
• Work efficiently in a clean-room manufacturing environment when required.
• Follow all safety guidelines and standard operating procedures.
• Support production goals while maintaining quality standards.
• Perform additional production-related duties as assigned.

• High school diploma or equivalent preferred.
• Previous manufacturing or production experience is a plus.
• Ability to work in a fast-paced environment with moderate supervision.
• Strong attention to detail and commitment to quality.
• Comfortable working in a clean-room environment when required.
• Ability to stand, walk, and perform repetitive tasks throughout the shift.
• Reliable attendance and strong work ethic.

• Employment Type: 6 Month Contract with possibility of extensions
• Location: Altavista, VA
• Pay Rate: $13.00- $15.55/hour
• Shift: 2nd Shift (3:00 PM – 11:30 PM)
• Overtime: Hours worked over 40 per week are paid at time and one-half in accordance with applicable regulations.

• Maintain accurate inventory records through physical and ERP inventory transactions.
• Perform material movements and ensure materials are delivered to production areas on schedule.
• Generate, receive, and process work orders within the ERP system.
• Conduct routine cycle counts and reconcile inventory discrepancies.
• Support manufacturing and assembly operations by providing timely material availability.
• Maintain a clean, organized, and safe work environment while following all safety procedures.
• Collaborate effectively with cross-functional teams to meet production goals.
• Safely handle chemicals, including IPA and sulfuric acid, after completing required training.
• Work overtime as needed to support business requirements.
• Comply with Quality Management System (QMS), Environmental Management System (EMS), and FDA regulations.
• Perform additional duties as assigned.
  
  

• High school diploma or GED required.
• Minimum of 1 year of inventory control experience, preferably in a regulated environment such as medical device or pharmaceutical manufacturing.
• Experience using ERP systems for inventory and material transactions.
• Strong attention to detail and organizational skills.
• Ability to work independently and collaboratively within a team.
• Commitment to workplace safety and quality standards.
• Ability to lift, move, and handle materials in a manufacturing environment.
  
  

• Perform manufacturing processes in compliance with SOPs.
• Ensure quality control throughout production workflows.
• Operate and maintain manufacturing equipment.
• Follow GMP and safety regulations.
• Assist with troubleshooting and process improvements.

•   High School Diploma or GED required.
• Zero to five years of experience.
• Experience working in a manufacturing environment.
• Strong problem-solving skills.
• Excellent communication abilities.
• Knowledge of industry best practices.
• Detail-oriented.
• Ability to lift 30 pounds.

• Experience in diagnostics or pharmaceutical manufacturing.

•  Assemble, repair, and test pacemakers, ICDs, leads, and related medical device assemblies. 
•  Perform precision assembly using microscopes throughout the shift. 
•  Handle and assemble small components with accuracy and attention to detail. 
•  Perform visual inspections to ensure products meet quality standards. 
•  Follow detailed work instructions, SOPs, and manufacturing procedures. 
•  Document production activities and maintain accurate records. 
•  Maintain a clean, organized, and safe work environment. 
•  Collaborate with team members to meet daily production goals. 

• Manufacturing experience is required.
•  Previous assembly experience in a manufacturing environment. 
•  Experience using microscopes for detailed assembly or inspection. 
•  Quality inspection experience. 
•  Ability to perform repetitive, detail-oriented work. 
•  Basic computer skills, including Microsoft Word and Excel. 
•  Strong communication and teamwork skills. 
•  Ability to multitask and work in a fast-paced production environment. 

•  Medical device manufacturing experience. 
•  Experience assembling or testing small electronic or mechanical components. 
•  Familiarity with regulated manufacturing environments (FDA/GMP).

• Promote and maintain a proactive culture of health, safety, and environmental compliance.
• Provide HSE support across all production areas and warehouse operations.
• Conduct routine shop floor inspections, safety observations, audits, and compliance assessments.
• Apply and reinforce Stop Work Authority when unsafe conditions exist.
• Coach and empower employees to actively participate in workplace safety initiatives.

• Ensure compliance with applicable OSHA regulations, environmental requirements, permits, and company policies.
• Conduct hazard assessments, risk evaluations, and Job Safety Analyses (JSAs).
• Review, update, and deploy Safe Work Procedures.
• Track corrective actions and compliance tasks through the HSE Management System (MST).

• Deliver HSE orientation and ongoing safety training for employees.
• Participate in daily Shift Starter and Tier 1 production meetings.
• Build strong partnerships with production teams to improve overall safety performance.
• Communicate HSE expectations clearly across all levels of the organization.

• Conduct and support incident investigations and root cause analyses.
• Develop corrective and preventive actions focused on continuous improvement.
• Monitor HSE performance metrics and recommend process improvements.
• Support ISO-based management systems and continuous safety initiatives.

• 5+ years of Health, Safety & Environmental (HSE) experience with a strong emphasis on industrial safety.
• In-depth knowledge of HSE regulations, OSHA requirements, and industry best practices.
• Experience supporting manufacturing, industrial, or production environments.
• Proven ability to build positive working relationships with production teams and leadership.
• Experience conducting incident investigations and implementing corrective actions.
• Strong communication, organizational, and problem-solving skills.
• Ability to spend significant time on the manufacturing floor.

• Bachelor's degree in Occupational Health & Safety, Environmental Science, or a related field.
• OSHA 30-Hour Certification (completed or in progress).
• Experience in manufacturing, mechanical construction, welding, or heavy industrial environments.
• Familiarity with ISO 45001 Occupational Health & Safety Management Systems.
• Demonstrated ability to engage employees at all organizational levels and promote a strong safety culture.

• Health & Safety (HSE)
• Industrial Safety
• OSHA Compliance
• Risk Assessments
• Safety Audits
• Incident Investigation
• Job Safety Analysis (JSA)
• Manufacturing Safety
• Regulatory Compliance
• Safety Training

• Site-based interview.
• Candidates should be prepared to discuss previous industrial safety experience, incident investigations, OSHA compliance, and examples of improving safety culture within manufacturing or industrial operations.

• Architect, deploy, and support IT and OT solutions for manufacturing operations.
• Provide operational support for on-premises network infrastructure, from SD-WAN-based Enterprise Wide Network (EWN) to sensor-level communications.
• Support Manufacturing and Site Network Infrastructure in both virtual and physical environments.
• Support Cisco-based LAN, WLAN, and IoT communication technologies.
• Migrate the site from an EWN/global authentication model to a site-level domain controller authentication model.
• Develop and deploy Special Use Networks (SUN) to secure semiconductor manufacturing environments.
• Collaborate with process, equipment, and advanced manufacturing engineering teams to enable network-level equipment integration and automation.
• Troubleshoot network performance issues across the IT/OT architecture.
• Support implementation and rollout of switches, firewalls, wireless infrastructure, and monitoring tools.
• Participate in cross-functional meetings with site and corporate teams to resolve network-related issues.
• Attend daily factory systems and manufacturing operations tier meetings to provide network support and updates.
• Work closely with Corporate IT and Global Security teams to ensure compliance with cybersecurity standards.
• Maintain network documentation, including topology diagrams, configuration records, and change logs.
• Ensure network resilience, redundancy, and high availability through proper design and proactive maintenance.
• Monitor and manage network health, performance, and capacity using appropriate tools and dashboards.
• Support AI-based semiconductor automation, equipment integration, Fault Detection and Classification (FDC), and Advanced Process Control (APC) infrastructure.

• Education: Bachelor's degree in Information Technology or a related field.
• Experience: 5+ years of experience supporting enterprise and industrial network infrastructure in manufacturing or site environments.
• Hands-on experience with Cisco networking and routing equipment.
• Strong background supporting factory floor networking (Level 2/3 OT) and collaboration with IT networks (Level 3.5/4).
• Proficiency with: Firewall configuration, VPN setup, VLANs, Subnetting, IP addressing, DNS, DHCP, NAT, Routing, Switching.
• Experience with high availability, redundancy, and Quality of Service (QoS) protocols.
• Experience with network segmentation, resilience, and disaster recovery strategies.
• Familiarity with DevOps network operations, including:
  • CI/CD integration for network changes 
  • Infrastructure as Code (IaC)
  • Monitoring and alerting pipelines
• Version control and automated deployment
• 2+ years of experience with PowerShell scripting.
• 1+ years of experience with Service Management platforms (e.g., ServiceNow).
• Strong ability to document network architecture, automation scripts, and system configurations.

• Advanced degree in Information Technology, Computer Science, Computer Engineering, or a related field.
• Cisco Certified Network Associate (CCNA) certification or equivalent.
• Experience with multi-vendor network equipment (e.g., Cisco, Arista, Dell, Palo Alto).
• Experience with network patching tools (e.g., Tanium, CHEF) and network security hardening practices.
• Experience supporting data protection and recovery platforms (e.g., Rubrik, Veeam, Commvault, Zerto).
• Strong understanding of IT/OT convergence, including:
  • Industrial protocols 
  • SCADA systems 
  • MES platforms
  • Equipment integration 
  • Manufacturing-focused Windows-based PCs and servers
• Knowledge of industrial network architectures, including layered models, DMZs, secure remote access, and redundant topologies.
• Demonstrated ability to drive organizational change, improve processes, and promote cross-functional collaboration.
• Excellent oral, written, and interpersonal communication skills.
• Strong problem-solving and solution design abilities.
• Highly self-motivated with the ability to work independently with minimal supervision.

• Accurately store and organize products within the warehouse.
• Prepare customer orders for shipment according to established processes and quality standards.
• Label, meter, and process shipments using multiple freight systems.
• Process customer orders using the Abbott ERP system.
• Perform daily preparations for upcoming shipping activities.
• Maintain a clean, organized, and safe warehouse environment.
• Support divisional initiatives related to Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
• Follow all company safety procedures and warehouse policies.
• Assist with additional warehouse duties as assigned.

• High School Diploma or equivalent required.
• Previous warehouse, shipping, receiving, or distribution experience is preferred.
• Experience with ERP systems is a plus; Abbott ERP experience is highly desirable.
• Strong attention to detail and accuracy.
• Ability to work in a fast-paced environment while meeting productivity and quality expectations.
• Strong communication and teamwork skills.

• Closed-toe shoes must be worn at all times.
• Long pants are required; shorts are not permitted.
• Pants must be worn at waist level, with undergarments not visible.
• Hats of any type are prohibited.
• Hooded sweatshirts are permitted; hoods must remain down.
• Tank tops and cutoff shirts are prohibited.
• Clothing displaying offensive slogans, pictures, words, or images is not permitted.
• Sunglasses may not be worn on the distribution center floor.

Senior Database Engineer

• Design, deploy, and maintain high-availability Microsoft SQL Server databases supporting manufacturing applications.
• Support operational databases for manufacturing systems, MES, SCADA, Historian, and enterprise applications.
• Perform advanced database tuning, optimization, monitoring, and troubleshooting.
• Develop complex SQL stored procedures, functions, views, and database objects.
• Design and implement SSRS and Power BI reports, dashboards, and analytics solutions.
• Migrate legacy reporting systems to modern data warehouse and data mart architectures.
• Support Oracle and DB2 databases as business needs require.
• Perform database modeling, architecture, and application-integrated database engineering.
• Develop PowerShell automation scripts for database administration and maintenance.
• Maintain database security, user access, migrations, backup, recovery, and disaster recovery processes.
• Document database architecture, configurations, automation, and operational procedures.
• Support 24/7 manufacturing operations by resolving critical database issues and outages.
• Collaborate with engineering, manufacturing, IT, and application teams to implement scalable database solutions.
• Mentor team members on SQL development and database best practices.
• Participate in software development lifecycle activities including requirements gathering, design, testing, deployment, and production support.

• Bachelor's degree in Computer Science, Computer Engineering, Information Technology, Software Engineering, or a related technical field.
• Minimum 5 years of hands-on Microsoft SQL Server experience.
• Minimum 5 years of database tuning and performance optimization experience.
• Minimum 5 years of SQL Server Management Studio (SSMS) experience.
• Minimum 2 years of PowerShell scripting experience.
• Experience with ServiceNow or a comparable IT Service Management platform.
• Strong experience with:
  • Microsoft SQL Server
  • Oracle
  • DB2
  • SQL Server Reporting Services (SSRS)
  • Power BI
  • Data Modeling and Database Design
  • Advanced SQL Development
  • Database Architecture and Governance
  • Performance-Driven Database Design
  • Application Integrated Database Engineering
  • Requirements-to-Design Translation
  • Greenfield database implementations
• Experience throughout the Software Development Lifecycle (SDLC).
• Strong documentation and technical communication skills.
• Ability to support critical manufacturing environments and respond to production incidents.

• Bachelor's degree in Computer Science, Software Engineering, Computer Engineering, Information Technology, or a closely related field required.
• Advanced degree preferred.

• Semiconductor manufacturing experience (Front-End or Back-End).
• Manufacturing Execution Systems (MES) support experience.
• Experience with SCADA and Historian databases.
• Experience with C#, HTML5, JavaScript, CSS, Python, and Microsoft Visual Studio.
• Experience with GitHub, Bitbucket, TFS, or similar source control systems.
• Experience supporting VB, VB.NET, ASP.NET, or other legacy technologies.
• Knowledge of ITIL methodologies.
• Experience with data protection, disaster recovery, and business continuity planning.
• Strong communication and stakeholder management skills.
• Experience supporting IT/OT environments.
• Proven ability to lead through critical outages and complex production issues.
• Self-driven with the ability to work independently.

• Assemble structural heart devices by following detailed work instructions and manufacturing procedures.
• Perform precision sewing using suture and needle under a microscope.
• Utilize microscopes, precision hand tools, and calibrated instruments to complete intricate assembly tasks.
• Inspect materials and components to verify compliance with quality specifications.
• Support product testing, validation, and manufacturing activities.
• Accurately document production activities while adhering to FDA, quality, and regulatory requirements.
• Maintain a clean and organized work environment while following cleanroom protocols.
• Perform additional duties as assigned.
  
  

• 0–2 years of manufacturing, assembly, or production experience.
• High School Diploma, GED, or equivalent experience preferred.
• Excellent hand dexterity with the ability to perform detailed, repetitive tasks.
• Strong attention to detail and commitment to producing high-quality work.
• Ability to follow written procedures and work instructions.
• Comfortable working under a microscope for extended periods.
• Experience using small hand tools and precision measuring equipment.
  
  

• Experience sewing with suture and needle.
• Previous cleanroom manufacturing experience.
• Experience in medical device manufacturing or another highly regulated industry.
  
  

• Architect, deploy, and support IT and OT solutions for a mission-critical manufacturing environment.
• Provide operational support for on-premises server infrastructure, including both virtual and physical environments.
• Work with corporate IT teams to maintain infrastructure standards while supporting 24x7 manufacturing operations.
• Support Hyper-Converged Infrastructure platforms such as Dell VXRail.
• Troubleshoot performance issues related to virtualized and physical server workloads.
• Implement new technology stacks and migrate workloads from physical servers to virtualized environments.
• Collaborate with semiconductor process and equipment vendors to improve infrastructure performance and fault tolerance.
• Participate in meetings with site and corporate teams to troubleshoot application and infrastructure issues.
• Participate in daily factory systems and manufacturing operations tier meetings.
• Partner with Corporate IT and Global Security teams to maintain cybersecurity standards across infrastructure.

• Education: Bachelor's Degree.
• Experience: Candidates must have proven hands-on Kubernetes experience in production environments. Experience limited to coursework, tutorials, or lab environments is not sufficient.
• 5+ years of experience supporting enterprise server ecosystems.
• 5+ years of experience with Windows Server OS and RHEL Linux 5–9.x.
• 3+ years of experience with ServiceNow or a similar formal Service Management platform and/or methodology.
• 3+ years of experience with virtualization platforms including VMware, vSAN, vSphere, and VCF/NSX.
• 1+ years of hands-on experience with Docker and Kubernetes for container orchestration.
• Proven production experience implementing and managing Kubernetes environments.
• Experience with one or more of the following: Server automation, Infrastructure as Code, Tanium, CHEF, JSON, PowerShell, Ruby, Other scripting languages
• Experience with networking fundamentals including: Firewall configuration, VPN setup, VLANs, Subnetting, IP addressing, DNS, DHCP, NAT, Routing, Switching
• Experience with backup, disaster recovery, and technology resilience strategies.
• Ability to document infrastructure, automation scripts, and system configurations to ensure maintainability and operational continuity.

• Advanced Degree in Information Technology, Computer Science, or Computer Engineering.
• Experience with Windows patching tools such as Tanium.
• Knowledge of Windows security standards and OS hardening concepts.
• Experience throughout the software development lifecycle, including: Requirements gathering, Design, Coding, Testing, Production support.
• Experience supporting Cisco Nexus and Catalyst network switches.
• Experience supporting Rubrik data recovery solutions.
• Experience supporting IT/OT systems and applications, including:
• Network implementation and segmentation
• Equipment integration and automation
• Manufacturing Execution Systems (MES)
• Understanding of: SCADA systems, Manufacturing-focused Windows PCs and servers, Industrial network architectures.
• Ability to serve as a change agent and promote organizational improvements.
• Excellent oral, written, collaborative, and communication skills.
• Ability to partner with internal customers at all organizational levels to define problems, identify solutions, and facilitate change.
• Self-motivated and self-driven with the ability to work efficiently with minimal supervision.

• Provide technical engineering support for validations, write, and execute Installation Qualification (IQ) protocols, and provide data to write completion reports for assigned validations.
• Provide technical engineering support for validations, write, and execute Operational Qualification (OQ) protocols, and provide data to write completion reports for assigned validations.
• Provide technical engineering support for validations, write, and execute Performance Qualification (PQ) protocols, and provide data to write completion reports for assigned validations.
• Provide technical engineering support for validations, write, and execute Computer Systems Validation (CSV) protocols.
• Provide technical engineering support for validations, write, and execute Test Method Validation (TMV) protocols.
• Provide technical engineering support for validations, write, and execute SAT (Site Acceptance Testing) validation protocols, and provide data to write completion reports for assigned validations.
• Responsible for running experiments during the pre-validation phase, run other experiments as needed.
• Ensure that assigned validation activities are performed in a timely manner and in accordance with current requirements and Good Manufacturing Practices (GMP).
• Demonstrate sufficient knowledge in validation skills, GMP, Good Documentation Practices (GDP).
• Responsible for the execution of validation, including the creation of forms to create calibration and preventive maintenance records.

• Engineering Degree (master’s in science is a plus)
• 4 – 5 years of experience in medical industry
• Good presentation skills before groups/clients.
• Solid skills in developing Factorial Experiments (DOE´s).
• Extensive knowledge in Lean.
• Intermediate knowledge in Six Sigma, DMAIC and Kaizen.
• Intermediate knowledge of Project Management.
• Extensive knowledge of statistics.
• Advanced English proficiency.

• Perform preventive, scheduled, and corrective maintenance on manufacturing and production equipment. 
• Troubleshoot and repair mechanical, electrical, pneumatic, and hydraulic systems to minimize equipment downtime. 
• Install, modify, and maintain manufacturing equipment while ensuring compliance with safety standards. 
• Conduct routine equipment inspections and perform safety checks. 
• Document maintenance activities, repairs, and preventive maintenance tasks using a Computerized Maintenance Management System (CMMS). 
• Maintain accurate maintenance records and equipment history. 
• Read and interpret technical drawings, blueprints, electrical diagrams, pneumatic schematics, and hydraulic schematics. 
• Utilize precision measuring instruments including micrometers, calipers, gauge pins, multimeters, and other diagnostic tools. 
• Support equipment inventory management by tracking replacement parts and maintenance components. 
• Collaborate with engineering, manufacturing, and production teams to identify equipment improvements and resolve technical issues. 
• Utilize systems such as Microsoft Office, SAP, Windchill, and Infor EAM (CMMS) to support maintenance activities. 
• Follow all company safety policies, quality standards, and manufacturing procedures. 
• Maintain a clean, organized, and safe work environment. 

• High School Diploma or equivalent. 
• Minimum of 2 years of industrial maintenance or automation experience. 
• Experience troubleshooting and repairing industrial production equipment. 
• Hands-on experience with industrial electrical systems, hydraulics, and pneumatics. 
• Strong understanding of maintenance practices, terminology, tools, and repair procedures. 
• Ability to accurately follow written and verbal work instructions. 
• Basic computer proficiency and experience using maintenance software or CMMS systems. 
• Strong mechanical aptitude and problem-solving skills. 
• Excellent communication and teamwork abilities. 

• 3–5 years of industrial maintenance experience. 
• Experience in a regulated manufacturing or medical device environment. 
• Familiarity with SAP, Windchill, or Infor EAM (CMMS). 
• Experience supporting automated manufacturing equipment.

• Build, debug, refine, and maintain steady-state and transient thermal models using Numerical Propulsion System Simulation (NPSS).
• Develop and maintain customer-specific NPSS engine models.
• Perform turbine engine performance and operability analyses throughout the product lifecycle.
• Support engine definition activities during all phases of New Product Introduction (NPI).

• Perform systems requirements analysis and requirements decomposition.
• Support Model-Based Systems Engineering (MBSE) initiatives.
• Integrate NPSS models with MBSE tools, including Cameo, when applicable.
• Validate system models and ensure technical accuracy across engineering programs.

• Mentor engineers on NPSS modeling techniques and best practices.
• Promote knowledge sharing and technical growth within the engineering organization.
• Lead technical discussions and provide engineering guidance to multidisciplinary teams.
• Solve complex engineering problems involving propulsion system performance and operability.

• Collaborate with systems engineering, design, test, and program management teams.
• Prepare and present technical reports and engineering analyses to leadership and customers.
• Support engineering reviews and customer meetings.
• Adapt to changing program priorities while managing multiple technical assignments.

• Bachelor's degree in Engineering, Aerospace Engineering, Mechanical Engineering, or another related technical discipline.
• Minimum 7 years of experience in gas turbine engine performance and operability modeling and analysis.
• Extensive experience using Numerical Propulsion System Simulation (NPSS).
• Strong understanding of:
• Gas turbine engine thermodynamics
• Steady-state engine performance
• Transient engine performance
• Aerospace propulsion systems
• Experience performing systems requirements analysis and decomposition.
• Excellent analytical, communication, and problem-solving skills.
• Ability to work independently while collaborating across multidisciplinary engineering teams.

• Experience working within Model-Based Systems Engineering (MBSE) environments.
• Experience integrating NPSS models with Cameo or similar MBSE platforms.
• Experience mentoring engineers and leading technical teams.
• Strong presentation and technical writing skills.
• Experience supporting commercial and military aerospace propulsion programs.
• Demonstrated success solving complex engineering challenges involving turbine engine systems.

• Numerical Propulsion System Simulation (NPSS)
• Gas Turbine Engine Performance
• Engine Operability Analysis
• Thermal Systems Modeling
• Model-Based Systems Engineering (MBSE)
• Cameo
• Aerospace Propulsion
• Systems Engineering
• Requirements Analysis
• Technical Leadership

•  Develop, refine, and substantiate promotional and non-promotional claims using clinical trial data, prescribing information, and peer-reviewed literature. 
•  Create annotated references and claim substantiation packages ready for MLR review and approval. 
•  Write high-quality medical content across multiple channels, including: 
  •  Healthcare Professional (HCP) materials 
  •  Patient education resources 
  •  Disease-state education 
  •  Congress presentations and panels 
  •  Digital marketing assets 
  •  Video scripts 
  •  Sales and promotional materials 
•  Ensure all promotional content maintains fair balance, accurate Important Safety Information (ISI), and on-label compliance. 
•  Partner with Medical Affairs and Regulatory teams to proactively address reviewer feedback and develop compliant alternatives. 
•  Collaborate with creative teams to integrate scientific accuracy with impactful messaging and visual storytelling. 
•  Maintain claim libraries, references, and documentation to support future content development and consistency. 

•  5–8 years of medical writing experience within pharmaceutical, biotechnology, or medical communications environments. 
•  Demonstrated experience writing, substantiating, and defending promotional claims through the MLR review process. 
•  Strong understanding of claim substantiation standards, referencing conventions, and regulatory expectations. 
•  Excellent ability to interpret: 
  •  Clinical trial data 
  •  Scientific publications 
  •  Prescribing Information (PI) 
•  Knowledge of: 
  •  FDA/OPDP promotional regulations 
  •  Fair balance requirements 
  •  Important Safety Information (ISI) standards 
•  Proficiency with AMA style guidelines. 
•  Exceptional writing skills with the ability to communicate effectively to healthcare professionals, patients, and internal stakeholders. 
•  Outstanding attention to detail with strong annotation, referencing, and document version control skills. 

•  Advanced degree in Life Sciences (PharmD, PhD, MS) or equivalent scientific background. 
•  Experience using Veeva Vault PromoMats annotation workflows. 
•  Oncology, immunology, biologics, or specialty pharmaceutical experience. 
•  Previous experience supporting an in-house creative studio or embedded content team. 

• Employment Type: W2 Contract NO C2C
• Duration: 3 Months 
• Schedule: Monday–Friday 
• Work Hours: 8:00 AM – 4:00 PM 
• Work Model: Hybrid (Onsite Tuesday, Wednesday, and Thursday) 
• Interview Process: Two interviews (45 minutes each) 

• Apply intensive and diversified knowledge of design principles, practices, and implementation for complex systems.
• Generate design concepts and participate in design reviews.
• Develop and test systems to assess performance against design specifications.
• Perform reliability testing and evaluate system interactions.
• Make independent engineering decisions.
• Apply advanced engineering knowledge to assigned projects.
• Participate in defining new components, products, or processes and identifying technical challenges.
• Create potentially patentable system components or processes.
• Plan and execute assigned engineering projects.
• Execute experiments and participate in experimental design.
• Utilize Design of Experiments (DoE) where appropriate.
• Participate in technical team activities.
• Share technical knowledge and expertise with others.
• Participate in project planning, process updates, and experimental design.
• Prepare and deliver presentations of project results.
• Monitor work quality and promote Quality First Time.
• Perform other duties as assigned by management.

• Develop Test Methods (TMV).
• Develop comprehensive testing plans.
• Execute hands-on testing protocols.
• Develop test beds.
• Analyze digital outputs from sensors.
• Perform data analysis, including Python coding.
• Author detailed technical reports.

• Assist in developing manufacturing processes.
• Troubleshoot engineering issues to determine root cause and recommend solutions.
• Manage the defect lifecycle, including collection, documentation, and summarization for the development partner.

• Education: Bachelor's degree in Engineering required. Preferred disciplines: Electrical Engineering, Chemical Engineering, Biomedical Engineering, Software Engineering.
• Experience: 8 years of engineering experience.
• Experience working with electro-mechanical devices.
• Experience with:
• Test Method Validation (TMV)
• Test Method Development
• Design of Experiments (DoE)
• Data analysis
• Python coding
• Sensor digital output analysis
• Test bed development
• Troubleshooting
• Test plan development
• Hands-on testing
• Technical report writing
• Defect lifecycle management.
• Knowledge, Skills, and Abilities
• Strong understanding of engineering principles and concepts.
• Technical proficiency.
• Engineering creativity.
• Collaboration with cross-functional teams.
• Independent thinking.
• Ability to work autonomously on complex assignments
  
  

• Experience in an FDA-regulated environment.
• Experience in an FAA-regulated environment.
• Medical device industry experience is ideal.

• Lead engineering workstreams for large-scale pharmaceutical capital projects, ensuring successful delivery within scope, schedule, and budget.
• Provide senior-level engineering expertise throughout all phases of project execution.
• Collaborate with site leadership, project teams, contractors, and construction management to drive timely project decisions.
• Identify, assess, and mitigate project risks while implementing effective solutions.
• Manage stakeholder communication and maintain strong working relationships across cross-functional teams.
• Review engineering drawings, specifications, construction submittals, RFIs, and scope changes.
• Ensure engineering deliverables comply with pharmaceutical manufacturing standards, cGMP requirements, and applicable regulations.
• Develop project specifications based on customer and operational requirements.
• Drive project schedules, documentation, and engineering decision-making for assigned workstreams.
• Support qualification, validation, and commissioning activities for cleanroom and classified manufacturing spaces.
• Promote continuous improvement while maintaining project quality, safety, and regulatory compliance.

• Bachelor's degree in Engineering required; Process Engineering background preferred.
• Minimum of 15 years of experience leading capital engineering projects.
• Extensive experience with pharmaceutical or life sciences manufacturing projects.
• Strong experience with cleanroom design, classified Grade C/D spaces, qualification, and validation.
• Brownfield project experience is highly preferred.
• Mechanical, Electrical, or Process Engineering background.
• Strong knowledge of pharmaceutical manufacturing regulations and current Good Manufacturing Practices (cGMP).
• Ability to interpret engineering drawings, specifications, and technical documentation.
• Proven leadership, negotiation, and stakeholder management skills.
• Strong communication and collaboration skills within matrix organizations.
• Demonstrated ability to independently manage engineering workstreams, schedules, risks, and documentation.
• Excellent analytical, problem-solving, and decision-making abilities.
• Ability to travel to and work onsite in St. Louis, Missouri, Monday through Friday.

• Experience leading large pharmaceutical facility expansion projects.
• Expertise in cleanroom construction and commissioning.
• Experience managing contractors, construction activities, and engineering teams.
• Experience reviewing RFIs, submittals, and construction documentation.
• Knowledge of life sciences manufacturing processes and facility operations.
• Experience working on ADC (Antibody Drug Conjugate) manufacturing or similar pharmaceutical expansion projects.

1. Do you have at least 5 years of experience conducting such analysis to predict critical speed, create whirl speed map or Campbell diagram, & predict displacement, force, & moment due to imbalance?

• Lead the mechanical design and development of aerospace components and systems from concept through production.
• Collaborate with systems engineering, manufacturing, and quality teams to ensure design feasibility, manufacturability, and compliance with aerospace standards.
• Develop and review detailed mechanical drawings, specifications, and design documentation.
• Conduct design reviews, risk assessments, and failure mode analyses to ensure robust and reliable designs.
• Mentor and guide junior engineers and provide technical leadership within the mechanical design team.
• Engage with customers and suppliers to align design requirements and resolve technical challenges.

• Education: Bachelor's or Master's degree in Mechanical Engineering or a related technical field.
• Experience: Minimum of 6 years of experience in project engineering or related roles within the aerospace industry.
• Experience: Extensive experience in mechanical design engineering within aerospace or related industries, focusing on complex components and system design.
• Proficiency in FEA software such as ANSYS APDL or ANSYS Workbench.
• Proficiency in 1D Beam-based FEA techniques.
• Proficiency in Rotor Dynamics & Shafting Structural Analyses.
• Ability to lead design reviews, conduct risk assessments, and mentor engineering teams effectively.
• Proven leadership experience managing mechanical design projects in aerospace environments.

• Strong problem-solving skills and attention to detail.
• Familiarity with systems engineering principles and cross-disciplinary collaboration.
• Experience with Product Lifecycle Management (PLM) tools and aerospace certification processes.
• Knowledge of aerospace materials, manufacturing processes, and design standards such as AS9100 and MIL-STD.
• Experience with design for manufacturability, tolerance analysis, and mechanical testing methodologies.

• Perform scheduled routine and non-scheduled calibrations on production and facilities equipment.
• Evaluate and update calibration standard operating procedures (SOPs).
• Suggest improvements to existing calibration methods and systems.
• Develop knowledge of manufacturing processes and equipment to identify calibration needs.
• Maintain the calibration status of all measuring and critical manufacturing equipment.
• Assist in establishing calibration and test methods for new and existing equipment.
• Accurately complete all calibration test records.
• Identify and report calibration failures.
• Develop calibration SOPs for new equipment.
• Revise calibration SOPs as required.
• Ensure calibration records are updated, maintained, and easily retrievable.
• Communicate business-related issues or opportunities to the next management level.
• Ensure compliance with all applicable federal, state, local, and company regulations, policies, and procedures.
• Demonstrate understanding and application of:
  • Data Integrity (DI) 
  • Good Manufacturing Practices (GMP) 
  • Good Documentation Practices (GDP)
• Perform other assigned duties as needed.
• Calibrate instruments that measure:
  • Distance 
  • Volume 
  • Pressure 
  • Vacuum 
  • Density
• Measurements to one ten-thousandth of an inch (0.0001)
• Work with external qualified calibration companies/agencies.

• Education: Associate's degree or equivalent.
• Experience: 2–4 years of related experience.

• Strong written and verbal communication skills.
• Good organizational skills with the ability to manage multiple tasks.
• Knowledge of manufacturing principles, practices, and procedures.
• Ability to communicate effectively with a diverse clientele.
• Ability to work cooperatively with coworkers and the public.
• Ability to perform duties in accordance with policies and procedures.
• Ability to work a flexible schedule, including overtime with minimal notice.
• Ability to work in a Class 10,000 clean room.
• Ability to wear cleanroom gowns.
• Ability to work in a clean room production environment.

• Technical writing skills.
• Experience with Maximo software.

• Perform visual and microscope-based inspections of microelectronic components.
• Inspect products to ensure compliance with quality standards and manufacturing specifications.
• Identify and document product defects or non-conformances.
• Maintain accurate inspection records and quality documentation.
• Follow established quality procedures, work instructions, and regulatory requirements.
• Utilize basic computer systems to document inspection activities.
• Maintain compliance with FDA regulations, Quality Management Systems (QMS), and company quality standards.
• Support continuous improvement initiatives within the quality organization.
• Maintain a clean and organized work area while following cleanroom procedures.
• Collaborate with production and quality teams to support manufacturing objectives.

• High school diploma or equivalent.
• Previous microscope experience is required.
• Experience performing hands-on product inspections in a manufacturing environment.
• Exceptional attention to detail and ability to perform repetitive inspection tasks.
• Ability to sit for extended periods throughout the shift.
• Basic computer skills.
• Ability to work in a cleanroom environment.
• Strong verbal and written communication skills.
• Ability to work the required Thursday–Sunday schedule.
• Willingness to work overtime on Fridays as needed.

• Medical device manufacturing experience.
• Experience inspecting microelectronics or electronic components.
• Experience working in FDA-regulated or cleanroom manufacturing environments.
• Familiarity with quality documentation and inspection procedures.
• Experience with electronic assembly or component manufacturing.

• Inspect raw materials and finished products to ensure they meet quality standards.
• Label and package products according to established work instructions and production requirements.
• Maintain accurate production records and documentation in accordance with Good Manufacturing Practices (GMP).
• Follow standard operating procedures (SOPs) and company quality guidelines.
• Support manufacturing operations while maintaining productivity and accuracy.
• Maintain a clean, organized, and safe work environment.
• Follow all safety procedures and wear required personal protective equipment (PPE).
• Report quality issues, equipment concerns, or production deviations to supervisors.
• Assist with general production activities as assigned.
• Work effectively under moderate supervision while contributing to team production goals.

• High school diploma or GED preferred.
• Previous manufacturing, production, packaging, or warehouse experience is a plus.
• Ability to read and follow written work instructions.
• Strong attention to detail and organizational skills.
• Ability to maintain accurate production documentation.
• Ability to work in a fast-paced manufacturing environment.
• Ability to stand for extended periods and perform repetitive tasks.
• Strong communication and teamwork skills.
• Willingness to work in a cleanroom environment if required.

• Experience working in a GMP-regulated manufacturing environment.
• Previous cleanroom manufacturing experience.
• Experience with product inspection, labeling, or packaging operations.

• Perform assembly, repair, and testing operations on pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related medical device assemblies.
• Follow established manufacturing procedures, work instructions, and quality standards.
• Maintain accurate production records, traveler documentation, and quality records to ensure product traceability.
• Support continuous improvement and quality initiatives to enhance manufacturing processes and product quality.
• Communicate production issues, solutions, and process updates effectively with supervisors and team members.
• Utilize electronic data collection systems and manufacturing software applications.
• Prioritize work assignments to meet production schedules and operational goals.
• Handle and maneuver small components and parts with precision.
• Participate in monitoring and achieving manufacturing performance metrics.
• Support Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
• Follow all safety procedures and properly utilize required safety equipment.
• Maintain a positive and professional attitude when interacting with internal teams and visitors.
• Work overtime as required to support production demands.
  
  

• High school diploma or equivalent.
• Ability to read, understand, and follow written procedures and verbal instructions.
• Basic computer proficiency and ability to utilize electronic data collection systems.
• Strong attention to detail and manual dexterity.
• Ability to handle and maneuver small components and parts.
• Ability to prioritize multiple tasks and meet production deadlines.
• Strong verbal and written communication skills.
• Ability to make sound decisions and exercise judgment with minimal supervision.
• Ability to work effectively in a team-oriented manufacturing environment.
• Willingness to work overtime as needed.
  
  

• Previous medical device manufacturing or assembly experience.
• Experience working in a regulated manufacturing environment.
• Familiarity with Lean Manufacturing principles.
• Experience maintaining production and quality documentation.
• Experience using electronic manufacturing systems and data collection tools.
  
  

•  Receive and inspect Commercial Off-The-Shelf (COTS) parts and custom machine components. 
•  Check in and organize incoming materials for machine builds. 
•  Monitor and track outstanding parts to ensure timely availability. 
•  Consolidate and stage COTS and machined components in preparation for assembly. 
•  Obtain, print, and organize required documentation, including TLAs, schematics, and work instructions. 
•  Coordinate with technicians, the machine shop, and internal requesters to resolve missing, incorrect, or delayed parts. 
•  Package, crate, and pallet completed machine kits for shipment. 
•  Notify requesters when kits are complete and ready for delivery. 
•  Maintain accurate records and support efficient material flow throughout the build process. 
•  Assist in maintaining an organized, clean, and safe work environment. 

•  High School Diploma or equivalent preferred. 
•  Strong organizational and multitasking abilities. 
•  Proficient with Microsoft Office, especially Word and Excel. 
•  Excellent communication and coordination skills. 
•  Strong attention to detail with the ability to prioritize multiple tasks. 
•  Mechanically inclined with a general technical understanding preferred. 
•  Basic familiarity with SolidWorks is preferred. 
•  Strong interpersonal skills with the ability to work effectively in a team environment. 
•  Ability to perform occasional physically demanding work, including lifting and material handling. 

•  Experience supporting manufacturing, machine assembly, or production environments. 
•  Familiarity with machine components, technical drawings, or assembly documentation. 
•  Experience coordinating materials and documentation for production or engineering teams. 

•  Ability to lift and move materials as needed. 
•  Frequent standing, walking, bending, and reaching throughout the workday. 
•  Ability to safely handle machine components and packaged materials.

• Inspect raw and finished products.
• Label raw and finished products.
• Package raw and finished products.
• Maintain records according to Good Manufacturing Practices (GMP), as required.
• Work in a clean-room environment, as required.

• Education: High School Diploma or GED required. 
• Ability to inspect, label, and package products.
• Ability to maintain records according to Good Manufacturing Practices (GMP), as required.
• Ability to work in a clean-room environment, as required.
• Ability to work under moderate supervision.

• Assemble, repair, inspect, and test implantable medical devices and related components.
• Follow detailed work instructions, manufacturing procedures, and quality standards.
• Complete routine production assignments with accuracy and attention to detail.
• Maintain accurate production records, travelers, and quality documentation to ensure full product traceability.
• Utilize electronic data collection systems and manufacturing software.
• Communicate production issues, ideas, and solutions effectively with supervisors and team members.
• Support Lean Manufacturing and continuous improvement initiatives.
• Meet established production, quality, and safety goals.
• Maintain compliance with Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
• Follow all safety procedures and properly use required personal protective equipment (PPE).
• Maintain a professional and positive attitude while interacting with coworkers, leadership, and facility visitors.

• High school diploma or equivalent preferred.
• Ability to read, understand, and follow written procedures and verbal instructions.
• Basic computer skills and ability to work with electronic manufacturing systems.
• Strong attention to detail and commitment to quality.
• Ability to prioritize tasks in a fast-paced manufacturing environment.
• Excellent hand dexterity and ability to work with small components and precision assemblies.
• Ability to make sound decisions with minimal supervision.
• Basic understanding of Lean Manufacturing principles is preferred.
• Strong communication and teamwork skills.

• Wearing required cleanroom garments and PPE.
• Wearing clean, non-shedding clothing appropriate for a controlled manufacturing environment.
• No open-toed shoes, artificial nails, nail polish, excessive jewelry, or strong fragrances.
• Following all contamination control and safety guidelines.
• Maintaining professional appearance standards required for cleanroom operations.

• Provide leadership within the Quality Operations department to ensure quality objectives and goals are achieved.
• Help develop and drive the strategic direction of quality operations and compliance initiatives.
• Conduct failure investigations and collaborate with business partners to implement robust corrective solutions that prevent recurring quality issues.
• Review pending investigation reports requiring Quality Assurance approval.
• Coach and train employees responsible for generating investigations.
• Escalate extraordinary investigation situations to Quality Assurance management for final approval.
• Support the facility in identifying and eliminating compliance risks.
• Ensure appropriate specifications and procedures related to products are utilized.
• Ensure adherence to compliance requirements and policies related to:
  • Marketing companies 
  • External manufacturers 
  • Packaging and labeling 
  • Product testing 
  • Returned goods 
  • Product complaints 
  • Product recalls
• Support, consult, train, and lead quality improvement projects focused on reducing defects, minimizing waste, and increasing reliability.
• Utilize Quality Engineering tools and techniques to:
• Establish sampling plans
  • Develop quality plans 
  • Conduct and participate in FMEA activities 
  • Support reliability engineering activities 
  • Conduct process and system audits 
  • Support specification development
• Analyze routine and test data to identify improvement opportunities.
• Provide statistical support for:
  • Sampling plan analysis 
  • Design of Experiments (DOE) 
  • Pareto analysis 
  • ANOVA 
  • Statistical Process Control (SPC) 
  • Other statistical applications as required
• Serve as technical reviewer for validation protocols and reports.
• Investigate nonconforming material and determine root cause, corrective actions, and disposition recommendations for the Material Review Board.
• Apply research and benchmarking activities to develop innovative quality solutions and support implementation.
• Develop and report progress on personal performance objectives aligned with facility quality goals.
• Prioritize work to meet established deadlines.
• Serve as the Quality Operations subject matter expert for assigned responsibility areas.
• Guide and coach Quality Operations Technicians in managing nonconforming product through the nonconforming system.
• Demonstrate independent application of:
  • Data Integrity (DI) 
  • Good Manufacturing Practices (GMP) 
  • Good Documentation Practices (GDP) 
• Communicate business-related issues and opportunities to the next level of management.
• Follow all Health, Safety, and Environmental practices.
• Ensure compliance with all federal, state, local, and company regulations, policies, and procedures.
• Perform other assigned duties as needed.

• Education: Bachelor's degree required. Strong preference for Engineering or a related technical field..
• Experience: Minimum of 4 years of related quality and manufacturing experience. Experience in an FDA-regulated environment. Experience in the medical device, pharmaceutical, or other highly regulated industry.

• Knowledge of ISO 13485 and/or cGMP regulations.
• Demonstrated project management and project leadership skills.
• Technical training and experience with:
  • Statistics 
  • Lean Manufacturing 
  • Six Sigma methodologies 
  • Measurement System Analysis (MSA) 
  • Statistical Process Control (SPC) 
  • Design of Experiments (DOE) 
  • Reliability methods
• Hands-on troubleshooting and problem-solving skills.
• Strong technical understanding of manufacturing equipment and processes.
• Knowledge of:
  • Quality System Regulation (21 CFR Part 820) 
  • ISO 13485 requirements 
  • Medical Device Directive (MDD) 
  • Canadian Regulations.

• ASQ Certification such as:
  • Certified Quality Engineer (CQE) 
  • Certified Quality Manager (CQM)
  • Certified Reliability Engineer (CRE) 
  • Certified Quality Auditor (CQA) 
• Six Sigma Certification (Green Belt, Black Belt, etc.).
• Process Excellence certification.

• Lead complex IT projects through the complete project lifecycle, from business case development to production release and operational transition.
• Develop project charters, including problem statements, scope definitions, timelines, budgets, resource plans, dependencies, stakeholder identification, and process maps.
• Plan, execute, monitor, and control project schedules, budgets, risks, and deliverables.
• Facilitate project kickoff meetings, workshops, and stakeholder meetings.
• Coordinate cross-functional teams including Business, IT, Engineering, Architecture, Information Security, Quality, and external vendors.
• Maintain project governance documentation and project compliance using enterprise project management tools.
• Manage project execution through all required tollgates while ensuring quality, cost, and schedule objectives are achieved.
• Ensure Information Security, Architecture, and compliance reviews are completed throughout the project lifecycle.
• Establish and stabilize ITIL operational processes for supported IT platforms.
• Define, monitor, and report key performance indicators (KPIs) for project success and operational readiness.
• Oversee vendor performance and ensure deliverables meet project expectations.
• Maintain project communications, executive presentations, and PMO reporting.
• Identify project risks, develop mitigation strategies, and manage issue resolution through production deployment and hypercare.
• Support transition of completed solutions to IT Operations teams.

• Bachelor's degree in Information Technology, Computer Science, Business, or a related field (or equivalent experience).
• Proven experience leading complex enterprise IT projects from initiation through implementation.
• Strong IT Project Management experience, including scope, schedule, cost, resource, and risk management.
• Experience implementing and stabilizing ITIL processes.
• Experience managing cross-functional stakeholders with competing priorities.
• Excellent communication, presentation, facilitation, and stakeholder management skills.
• Experience creating executive-level presentations and project status reporting.
• Ability to quickly learn and lead projects involving new technologies and business processes.
• Experience managing vendor relationships and project deliverables.
• Strong organizational and problem-solving skills.
• Experience overseeing compliance activities including Information Security and Architecture reviews.

• Experience supporting IT projects and enterprise systems.
• Experience using enterprise IT Project Portfolio Management (ITPPM) tools.
• PMP, PRINCE2, ITIL, Agile, or equivalent project management certifications.
• Experience leading enterprise digital transformation or process improvement initiatives.

• Provide technical engineering support for validations, write and execute Installation Qualification (IQ) protocols, and provide data to write completion reports for assigned validations.
• Provide technical engineering support for validations, write and execute Operational Qualification (OQ) protocols, and provide data to write completion reports for assigned validations.
• Provide technical engineering support for validations, write and execute Computer Systems Validation (CSV) protocols.
• Provide technical engineering support for validations, write and execute Test Method Validation (TMV) protocols.
• Responsible for running experiments during the pre-validation phase, run other experiments as needed.
• Ensure that assigned validation activities are performed in a timely manner and in accordance with current requirements and Good Manufacturing Practices (GMP).
• Demonstrate sufficient knowledge in validation skills, GMP, Good Documentation Practices (GDP).
• Responsible for the execution of validation, including the creation of forms to create calibration and preventive maintenance records.

• Engineering Degree (master’s in science is a plus)
• 3 – 4 years of experience in medical industry
• Good presentation skills before groups/clients.
• Intermediate knowledge in statistics.
• Intermediate knowledge in Six Sigma, DMAIC and Kaizen.
• Advanced English proficiency 
• Experience in validation activities and product knowledge of the following medical devices (MUST):
  •  OCTARAY™ Mapping Catheter 
  •  THERMOCOOL SMARTTOUCH™ SF (STSF – Surround Flow) Catheter 
  •  QDOT MICRO™ Catheter
•  Valid U.S. tourist visa and availability to travel (REQUIRED). 

• Create, modify, and maintain technical drawings, floor plans, and manufacturing layouts using AutoCAD and SolidWorks.
• Develop and update plant layouts to support production line expansions, equipment relocations, capacity increases, and continuous improvement initiatives.
• Coordinate layout revisions with Manufacturing, Facilities, Production, Quality, and Engineering teams.
• Generate detailed 2D and 3D drawings for manufacturing equipment, workstations, fixtures, and production areas.
• Ensure drawing accuracy, revision control, and compliance with engineering standards.
• Support Engineering Change Orders (ECOs) related to facility, equipment, and process modifications.
• Evaluate manufacturing floor changes and verify layout implementation on the shop floor.
• Assist in space utilization analysis, material flow optimization, and workstation design improvements.
• Maintain engineering documentation including layouts, drawings, BOMs, work instructions, and related records.
• Support manufacturing projects, equipment installations, validations, and process improvement activities.
• Participate in troubleshooting activities related to equipment, production flow, and facility modifications.

• Bachelor’s degree in Mechanical Engineering, Manufacturing Engineering, Mechatronics Engineering, Industrial Engineering, or related field.
• Minimum 2–4 years of experience in manufacturing environments.
• Advanced experience using AutoCAD.
• Intermediate to Advanced experience using SolidWorks.
• Proven experience updating and maintaining plant layouts (production lines, equipment moves, facility modifications, capacity expansions).
• Ability to interpret engineering drawings, specifications, and manufacturing documentation.
• Strong organizational, communication, and teamwork skills.
• Intermediate English proficiency (written and verbal).

• Experience in medical device, automotive, electronics, or regulated manufacturing industries.
• Knowledge of manufacturing processes and production flow optimization.
• Familiarity with Engineering Change Orders (ECOs) and document control systems. Experience supporting equipment installations, facility projects, and layout validations.
• Exposure to Lean Manufacturing concepts, including 5S, Kaizen, and Continuous Improvement.
• Knowledge of IQ/OQ/PQ validation activities is a plus.

• This position will be handled by Garima Bisht, kindly share resume on Garima.bisht@toyota.com
• Export Control form would be required but at the time of onboarding only and not required during submission.
• This position is with Enterprise Analytical Data & Integration Team and the hiring manager is looking to onboard MLOpsPlatform Engineer (Sagemaker) who is expert in Sagemaker and AWS (key skillsets).
• Local candidates preferred, 12 months contract with extension, Onsite role.

• 10-15 years of software engineering experience focused on cloud infrastructure or ML platform operations.
• 5+ years hands-on with AWS, including deep expertise in Amazon SageMaker (Studio Classic Studio, Pipelines, Model Registry, Endpoints, Feature Store)
• 3+ years building and operating production MLOps pipelines — training, versioning, deployment, monitoring, rollback
• Experience with SageMaker Unified Studio or Studio Classic — domain/project setup, blueprints, multi-tenant configuration
• MLflow or equivalent experiment tracking
• SageMaker Pipelines or similar workflow orchestration (Airflow, Step Functions)
• Unified Studio is preferred to have but Classic is must have.
   

• 1st Round- MS Teams - Technical Interview – SageMaker and AWS
• 2nd Round- MS Teams - Technical Interview – SageMaker and AWS

Pricing Analyst

• Conduct market research and price analysis to evaluate supplier pricing for commercial products and services.
• Analyze comparable commercial offerings to establish fair and reasonable pricing benchmarks.
• Apply FAR and DFARS regulations to ensure compliance across all pricing activities.
• Support pricing strategies for FAR Part 15 proposals, ensuring accuracy, compliance, and audit readiness.
• Develop detailed pricing analyses utilizing financial principles, market data, and analytical methodologies.
• Collaborate cross-functionally with business leaders, proposal teams, engineering, procurement, and subcontract specialists.
• Present pricing recommendations and insights to stakeholders to support strategic decision-making.
• Identify pricing risks and opportunities while developing innovative solutions to complex pricing challenges.
• Manage multiple priorities while maintaining exceptional attention to detail and accuracy.
• Prepare documentation supporting fair and reasonable pricing determinations.

• Bachelor's degree in Accounting, Finance, Economics, Business, Engineering, or a related field.
• Minimum of 3 years of experience in pricing, price analysis, FP&A, finance, accounting, or related disciplines.
• Experience working within FAR and DFARS regulatory environments.
• Strong analytical, critical thinking, and problem-solving abilities.
• Ability to develop creative and strategic pricing solutions.
• Excellent communication and stakeholder management skills.
• Strong organizational skills with the ability to manage multiple priorities simultaneously.

• Experience within aerospace, defense, or government contracting industries.
• Knowledge of FAR Part 15 proposal pricing requirements.
• Advanced proficiency with Microsoft Excel and data analysis tools.
• Experience conducting supplier price analysis and market benchmarking.
• Ability to present complex pricing concepts to technical and non-technical audiences.

• Pay Rate: $48.00 - $60.00/hour
• Schedule: Day Shift (7:00 AM - 4:00 PM or 8:00 AM - 5:00 PM)
• Location: 100% Onsite
• Time Reporting: Weekly time entry through designated timekeeping system
• Employment Type: Contract

1. Can you walk me through your experience performing price or cost analysis in a FAR/DFARS environment? What types of contracts or programs have you supported?
2. What pricing tools, financial analysis techniques, or systems have you used most frequently, and how would they support your success in this role?
3. Describe a time when you had to determine whether a supplier's price was fair and reasonable. What data and methodologies did you use, and what was the outcome?
4. How have you used market research to support pricing decisions? Please provide a specific example and explain how it influenced your final recommendation.

•  Perform preventive maintenance on HVAC/R systems, refrigeration equipment, chillers, boilers, and related facility systems. 
•  Troubleshoot mechanical, electrical, and controls-related issues to identify root causes and complete repairs. 
•  Maintain safe and reliable operation of facility equipment. 
•  Inspect, test, and repair components to ensure proper performance and compliance with site standards. 
•  Document maintenance activities, repairs, inspections, and equipment conditions. 
•  Support facility operations by responding to service requests and equipment issues in a timely manner. 

•  Experience maintaining and repairing HVAC/R systems, refrigeration equipment, chillers, and boilers. 
•  Strong troubleshooting skills across mechanical and related electrical systems. 
•  Ability to perform preventive maintenance and corrective repairs in an industrial or facility environment. 
•  Knowledge of safety practices related to HVAC/R and mechanical maintenance. 
•  Strong attention to detail, reliability, and communication skills. 

• Create, modify, and release technical drawings under direct supervision using AutoCAD and/or SolidWorks. 
• Adjust designs and layouts to meet project, manufacturing, and validation requirements.
• Develop visual guidelines and detailed drawings to support manufacturing processes. 
•  Document design codes, specifications, and compliance standards within drawings. 
• Support Engineering Change Orders (ECOs) related to parts, components, and manufacturing processes.
• Collaborate with associates, group leaders, supervisors, and engineering teams to review and implement design changes. 
• Assist with updates to manufacturing documentation, including Work Instructions, Bills of Materials (BOMs), routers, and travelers. 
• Support process and equipment troubleshooting activities as needed. 
• Participate in assessments, process validations, software validations, and database updates related to manufacturing and engineering changes.
• Work directly on the shop floor to evaluate the impact of design or component variations. 

• Currently pursuing or recently graduated from a Bachelor’s degree in Mechatronics Engineering, Manufacturing Engineering, Mechanical Engineering, or related fields.
• Minimum of 2 years of experience as a Design Technician / Designer within the maquiladora (manufacturing) industry.
• Upper-Intermediate experience using AutoCAD (preferred) and/or SolidWorks. 
• Ability to interpret technical drawings, specifications, and manufacturing documentation.
• Strong communication and teamwork skills.
• Intermediate English proficiency (written and verbal). 

•  Experience in the medical devices industry.
•  Familiarity with regulated manufacturing environments. 
• Exposure to validation activities (IQ/OQ/PQ) and engineering documentation control.