• Foreign Trade Zone (FTZ) Specialist

    ThermoFisher Scientific (Greenville, NC)
    **Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE ... be able to pass a comprehensive background check, which includes a drug screen.** We have industry-leading sterile injectable facilities providing solutions to take… more
    ThermoFisher Scientific (11/19/25)
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  • Maintenance Supervisor

    West Pharmaceutical Services (Williamsport, PA)
    …+ Supervise a multiple shift team in the maintenance and installation of pharmaceutical equipment consistent with high quality standards. + Initiates work orders and ... to achieve work goals. + Oversee technical support and training for all manufacturing equipment. + Write procedures for employees on various jobs and equipment.… more
    West Pharmaceutical Services (12/27/25)
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  • Sr. Director, Process Engineering

    West Pharmaceutical Services (Kinston, NC)
    …engineering team, with the goal to improve and standardize the current manufacturing processes within the containment network, encompassing the elastomer and seal ... manufacturing processes. This individual will leverage experience and knowledge from the pharmaceutical or other highly regulated industries to develop the team's… more
    West Pharmaceutical Services (12/13/25)
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  • MES Architect - IDAP Tech@Lilly

    Lilly (Indianapolis, IN)
    …EBR design, material traceability, and exception management. + Familiarity with pharmaceutical or medical device manufacturing processes, especially in packaging ... directly in PharmaSuite deployments. + 7+ years of experience in regulated pharmaceutical or medical device manufacturing environments. + Experience leading MES… more
    Lilly (12/12/25)
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  • Senior Engineer, Validation

    AbbVie (North Chicago, IL)
    …/ compliance management as well as regulations and standards affecting API, Bulk Drug or Finished goods manufacturing . + Strong knowledge of qualification and ... leading, planning, executing, and maintaining qualification/validation activities at AbbVie's manufacturing site. This role ensures that all systems are installed,… more
    AbbVie (12/11/25)
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  • Aseptic Process Technician/Operator (GMP)

    Mentor Technical Group (Durham, NC)
    …aseptic techniques. + Operate, monitor, and maintain equipment used in sterile drug product manufacturing . + Perform environmental monitoring and in-process ... or related field preferred. + Experience: 1-3 years of aseptic/sterile manufacturing experience in a GMP-regulated facility ( pharmaceutical , biotech, or… more
    Mentor Technical Group (12/10/25)
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  • Clean Room Warehouse Associate

    Adecco US, Inc. (Swiftwater, PA)
    …sterile, compliant production environments - a great entry point into pharmaceutical manufacturing . **Key Responsibilities** . Perform aseptic cleaning of ... Life-Saving Vaccines** Adecco is hiring Production Technicians to support vaccine manufacturing for one of the world's leading pharmaceutical companies in… more
    Adecco US, Inc. (12/03/25)
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  • Manager, Operations

    ThermoFisher Scientific (Greenville, NC)
    …may be considered. **Experience** + 5+ years of operations experience in pharmaceutical manufacturing or a related industry is preferred. **Knowledge, Skills, ... Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail… more
    ThermoFisher Scientific (11/19/25)
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  • Associate Director, Engineering & Maintenance

    Catalent Pharma Solutions (Manassas, VA)
    …expanded capabilities in soft chews and lozenges. With extensive development and manufacturing expertise and a wide range of flavors, ingredients, and colors ... will direct and lead a team of employees who support a 24 x 5 manufacturing facility. As a member of the site Senior Leadership Team, the position reports directly… more
    Catalent Pharma Solutions (12/23/25)
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  • Quality Control Analyst II

    Curia (Camarillo, CA)
    …lives. The Quality Control Analyst II is responsible for supporting the manufacturing department and external customers. Routine functions include testing of raw ... end product, and stability samples. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with … more
    Curia (12/12/25)
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