• Senior Director, R&D Quality Transformation…

    AbbVie (North Chicago, IL)
    …global teams. + 15+ years industry experience across pharmaceutical, medical device , combination products, research, development, clinical operations, ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...regulatory compliance, and contributes to the overall success of drug/ device development programs. The Sr Director, R&D Quality more
    AbbVie (11/25/25)
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  • Osteogenics Quality Associate (On-Site…

    Envista Holdings Corporation (Lubbock, TX)
    Quality position within an FDA regulated industry (ex: tissue banking, medical device , biologics or pharmaceutical industries. **PREFERRED QUALIFICATION:** + ... **Job Description:** **JOB SUMMARY** : The Quality Associate provides quality assurance services...and OpCo standards. **PRIMARY DUTIES & RESPONSIBILITIES:** + Review device batch records for accuracy and compliance to established… more
    Envista Holdings Corporation (11/22/25)
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  • Quality Engineer, Design Control

    Hologic (San Diego, CA)
    …experience in a regulated environment, ideally in the IVD space. + Working knowledge of Quality Management System for Medical Device Manufacturing FDA 21 CFR ... Quality Engineer, Design Control San Diego, CA, United...mark requirements, In Vitro Diagnostic Regulation (EU) 2017/746 and Medical Device Regulation (EU) 2017/745, Risk Management… more
    Hologic (11/21/25)
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  • Director of Design Quality Engineering-Oral…

    Philips (Bothell, WA)
    …Design Quality /Control with extensive experience in both ISO 13485 Medical Device /Technology and ISO 9001, with extensive design/development experience in ... The Director of Design Quality Engineering will play a critical role within...Class I medical device , consumer goods and cosmetics. +...Class I medical device , consumer goods and cosmetics. + You have proven… more
    Philips (11/04/25)
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  • Sr. Quality Engineer/C&Q

    Mentor Technical Group (Caguas, PR)
    … control, quality assurance, or regulatory compliance, preferably in the medical device or pharmaceutical industry Mentor Technical Group es un empleador ... the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas,… more
    Mentor Technical Group (11/01/25)
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  • Lab Service Quality Engineer

    BD (Becton, Dickinson and Company) (Temecula, CA)
    …experience in quality engineering, preferably in a combination product or medical device environment. + Strong knowledge of design control, risk management ... **Job Description Summary** The Lab Services Quality Engineer is responsible for ensuring quality...of possible** BD is one of the largest global medical technology companies in the world. Advancing the world… more
    BD (Becton, Dickinson and Company) (10/25/25)
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  • Sr Quality Manufacturing Engineer

    Philips (Murrysville, PA)
    …fit if:** + Bachelor's degree required. 5+ years of experience in a medical device or regulated industry (preferred). + Direct inspection engineering sustaining ... **Sr. Quality Manufacturing Engineer** **In this role you** Responsible...+ Basic understanding of CAPA, as well as global medical device regulations, requirements and standards such… more
    Philips (09/25/25)
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  • Quality Control Inspector 2

    Hologic (Marlborough, MA)
    …technical school education preferred. Minimum of 3 to 5 years related Quality Inspection experience in Medical Manufacturing environment. Experience with Oracle, ... Quality Control Inspector 2 Marlborough, MA, United States...facility to create a manufacturing process working on life-saving medical devices with potential for future growth. This is… more
    Hologic (09/25/25)
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  • Quality Engineer

    Actalent (Austin, TX)
    …experience, preferred; preferably in a FDA regulatory industry (ie, pharmaceutical, biomedical, medical device field) with an in-depth knowledge of current Good ... Quality Engineer Job Description * Provide Quality...and acceptance sampling within a regulated industry such as medical device manufacturing or pharmaceutical. * Personal… more
    Actalent (12/06/25)
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  • Lead Quality Inspector

    Integra LifeSciences (Plainsboro, NJ)
    …of overall corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. **This ... / Regulatory Compliance environment with a working knowledge preferably in the medical device , diagnostics or pharmaceutical industries. Familiarity with FDA… more
    Integra LifeSciences (11/05/25)
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