• Staff Quality Engineer I

    BD (Becton, Dickinson and Company) (Hunt Valley, MD)
    …of experience in sterilization , microbiological and/or supplier management in medical device and/or healthcare industry. + Demonstrated experience in ... **Job Description Summary** Sterilization , Validation & Supplier Management **Job Description** We...standards. Knowledge Management + Working knowledge of the FDA medical device quality system regulations and international… more
    BD (Becton, Dickinson and Company) (02/25/24)
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  • Senior Compliance Specialist

    ThermoFisher Scientific (Cambridge, MA)
    …regulatory requirements, including but not limited to the US FDA CFR, European Medical Device Directives (MDD, IVDD, AIMD) and European Regulations (MDR, IVDR), ... Medical Device Single Audit Program (MDSAP), and...with colleagues and business partners. + Develop and deliver auditor training materials for internal quality auditors across the… more
    ThermoFisher Scientific (03/29/24)
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  • Supplier Qual Engineer II

    Medtronic (North Haven, CT)
    …action (CAPA/SCAPA) + High-level Supplier Change request knowledge + Mastery of medical device quality systems and applications is required + Demonstrated ... plant operations preferred + Design Control knowledge preferred + Knowledge of sterilization methods preferred + Thorough understanding of the US and international… more
    Medtronic (04/26/24)
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  • Environmental Health & Safety Site Leader

    BD (Becton, Dickinson and Company) (Columbus, NE)
    …of 10 years of experience in a manufacturing environment. + Experience in Medical Device , Chemical, or Pharmaceutical manufacturing is preferred. + Experience ... and Safety programs for Pharmaceutical Systems and NAMc, including sterilization unit in compliance with BD corporate and local...of possible** BD is one of the largest global medical technology companies in the world. Advancing the world… more
    BD (Becton, Dickinson and Company) (03/10/24)
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  • Sr. Quality Engineer External Manufacturing

    Integra LifeSciences (Plainsboro, NJ)
    medical devices in conformance with the Quality System Regulation, ISO 13485, Medical Device Directive, ISO 14971, IEC 60601 and other regulatory standards. ... + BS in Engineering or associated scientific discipline. + Minimum 5 years Medical Devices or Pharmaceutical experience in Quality or R&D Engineering position. +… more
    Integra LifeSciences (04/16/24)
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  • Senior Supplier Quality Engineer

    Medtronic (Billerica, MA)
    …metal precision processing, and adhesives for the Catheter/Disposable SQE position. + Medical device manufacturing industry experience, preferably ISO 13485. + ... the only way to drive healthcare forward and remain a global leader in medical technology and solutions. **A Day in the Life** Medtronic is currently searching for… more
    Medtronic (04/16/24)
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