• Clean Room Manufacturing Operator

    Integra LifeSciences (Plainsboro, NJ)
    …plus. + 0 - 2 years of chemical processing experience or batch mixing in Medical Device or Pharmaceutical manufacturing industry. Production experience in a ... and set new standards of care. This **Clean Room Manufacturing Operator** role will include processes such as enzymatic...the setup, operation, and cleaning of all clean room manufacturing equipment. This entails working in ISO Class 5… more
    Integra LifeSciences (05/31/25)
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  • Manufacturing Operator II

    Integra LifeSciences (Plainsboro, NJ)
    …plus. * 0 - 2 years of chemical processing experience or batch mixing in Medical Device or Pharmaceutical manufacturing industry. Production experience in a ... pathways to advance patient outcomes and set new standards of care. This ** Manufacturing Operator II - 1st Shift** will perform post-formulation processing such as… more
    Integra LifeSciences (05/15/25)
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  • Cleanroom Manufacturing Operator

    Integra LifeSciences (Plainsboro, NJ)
    …+ 0 - 2 years of chemical processing experience or batch mixing in Medical Device or Pharmaceutical manufacturing industry. Production experience is highly ... outcomes and set new standards of care. This **Clean Room Manufacturing Operator** will perform post-formulation processing such as product cutting, inspection,… more
    Integra LifeSciences (04/17/25)
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  • Principal Associate - Quality Lead, Drug Product…

    Lilly (Indianapolis, IN)
    …assigned **Basic Requirements:** + At least 5 years of experience in pharmaceutical medical device and Packaging manufacturing /quality + Bachelor's Degree in ... responsible for assuring the CM maintains a state of control with regards to manufacturing , Device assembly and/or packaging product. The QA Lead is integral for… more
    Lilly (03/19/25)
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  • Manager, Manufacturing

    Integra LifeSciences (Plainsboro, NJ)
    …degree with 2+ years of experience leading a team + Experience in the Medical Device Industry supervising manufacturing functions, including clean room ... all established costs, quality, and delivery commitments are met, working within FDA medical device regulations, and applicable ISO standards. + Responsible for… more
    Integra LifeSciences (03/31/25)
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  • Jt525 - Manufacturing Engineer I

    Quality Consulting Group (Juncos, PR)
    …yellow belt or green belt + Process Validation and CSV Validation Knowledge + Medical device industry experience + Manufacturing support experience + ... QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and… more
    Quality Consulting Group (04/18/25)
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  • Manufacturing Technician (Weekend Shift)

    Aerotek (Longmont, CO)
    …requirements. **Qualifications:** + Proven experience working in a regulated environment (ie medical device , pharmaceutical or food manufacturing ) + Strong ... **Job Title: Manufacturing Technician** **Location: Longmont, CO** **Shift: Weekend Shift...equipment according to standard operating procedures (SOPs). + Assemble medical devices working with small parts. + Conduct inspections… more
    Aerotek (05/21/25)
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  • Sr. Facilities Technician, HVAC

    Terumo Medical Corporation (Elkton, MD)
    …for Medical Devices. + Comply with the requirements of a Cleanroom medical device manufacturing environment (ISO 14644-1) including gowning procedures, ... facilities related systems. + Familiarity with the requirements of a Cleanroom medical device manufacturing environment as outlined in ISO 14644-1, including… more
    Terumo Medical Corporation (04/10/25)
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  • Facilities Technician II, General Bldg

    Terumo Medical Corporation (Elkton, MD)
    …for Medical Devices. + Comply with the requirements of a Cleanroom medical device manufacturing environment (ISO 14644-1) including gowning procedures, ... facilities related systems. + Familiarity with the requirements of a Cleanroom medical device manufacturing environment as outlined in ISO 14644-1, including… more
    Terumo Medical Corporation (04/09/25)
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  • Senior Process Engineer II - CEA Controls

    Integra LifeSciences (Princeton, NJ)
    …as it relates to microbial monitoring and sterility assurance in a medical device manufacturing environment. **ESSENTIAL DUTIES AND RESPONSIBILITIES** ... matter experts responsible for implementing and optimizing contamination control programs in medical device manufacturing . + Foster a collaborative… more
    Integra LifeSciences (04/04/25)
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