• Supervisor , Quality Assurance

    Curia (Hopkinton, MA)
    …5 to 8 years' experience in Quality Assurance in the pharmaceutical/biotechnology or medical device industry experience, including 2 years in a leadership role ... SUPERVISOR , QUALITY ASSURANCE in Hopkinton, MA Build your...save lives Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience… more
    Curia (05/31/25)
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  • GMP Engineering Supervisor

    Caris Life Sciences (Phoenix, AZ)
    …environment. + Demonstrated knowledge of equipment qualification and validations strategies for medical device manufacturing or a related product ... Caris is where your impact begins.** **Position Summary** The GMP Engineering Supervisor is responsible for assisting in company-wide compliance to all applicable… more
    Caris Life Sciences (07/30/25)
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  • Maintenance Supervisor - Parenteral - Night…

    Lilly (Durham, NC)
    …+ Knowledgeable of Parenteral Maintenance operations and processes or other GMP manufacturing experience + Formulation, Filling, Device Assembly or Packaging ... solutions to support communities through philanthropy and volunteerism. The Maintenance Supervisor is responsible for the technical and administrative leadership of… more
    Lilly (07/31/25)
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  • Equipment Supervisor

    Medtronic (North Haven, CT)
    …will be responsible for day-to-day and preventative equipment support and maintenance in a medical device manufacturing area that produces materials used for ... Day in the Life** Job Specific Summary Join Medtronic as an Equipment Support Supervisor and lead a team that is dedicated to transforming healthcare technology. In… more
    Medtronic (07/31/25)
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  • Production Supervisor -Gamma Dr.

    ZOLL Medical Corporation (Pittsburgh, PA)
    …innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and ... (https://cardiacdiagnostics.zoll.com/products/heart-failure-arrhythmia-management-system/) (Heart Failure Management system) is a non-invasive, patch-based device that monitors pulmonary fluid levels and has been… more
    ZOLL Medical Corporation (07/08/25)
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  • Supervisor , Quality Control Chemistry

    Cardinal Health (Indianapolis, IN)
    …21 CFR 210, 211 in the FDA regulated industry preferred (Pharmaceutical or Medical Device ). + Must have experience with equipment qualification, software ... to making a difference for our customers and communities. **_What a Supervisor , Quality Control (Chemistry) contributes to Cardinal Health_** Quality Control is… more
    Cardinal Health (07/18/25)
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  • Equipment Engineering Supervisor - 1st…

    Abbott (Westfield, IN)
    …experience + Production ramp up experience + Experience designing and testing medical devices + Experience developing manufacturing processes and technologies ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
    Abbott (06/27/25)
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  • Supervisor , Quality Control

    West Pharmaceutical Services (Jersey Shore, PA)
    …Basic Lean and/or ISO working experience. + Preferably with exposure to medical device , pharmaceutical or related manufacturing environment. **Preferred ... Supervisor , Quality Control Requisition ID: 70201 Date: Aug...involves sitting most of the time. **Additional Requirements** + Manufacturing environment with rotating working shift patterns + Overtime… more
    West Pharmaceutical Services (06/07/25)
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  • Equipment Management Supervisor

    American Red Cross (Gaithersburg, MD)
    …may be required. + Knowledge of operations in biologics, pharmaceutical, or medical device - manufacturing environment required. Knowledge of federal ... regulatory and quality assurance practices/principles related to medical industry manufacturing required. Refrigeration knowledge preferred. + Ability to… more
    American Red Cross (07/23/25)
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  • Document Control Supervisor

    Zimmer Biomet (Warsaw, IN)
    …Maintain Document Control program to ensure compliance to domestic and international medical device regulations through supervision of Document Control and/or ... plus. + Minimum of 8 years combined industry (biomedical, medical device ) and/or military experience; or 10...10 years of combined industry, military and/or related (general manufacturing , quality or logistics) experience. + A combination of… more
    Zimmer Biomet (07/08/25)
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