• Senior Staff Biocompatibility Scientist

    Stryker (Tempe, AZ)
    …assess biocompatibility test plans, data, and special process validations for medical device cleaning and reprocessing. + Risk-Based Change Assessment: ... experience, including 4+ years leading technical biocompatibility projects in the medical device industry, with proven expertise in biological evaluation… more
    Stryker (11/22/25)
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  • Clinical Research Associate Manager (Remote)

    Teleflex (Minneapolis, MN)
    …ability to be detail-oriented, organized, and productive with a keen interest in medical device and biologics research. **Principal Responsibilities** * Manage a ... its goals of follow-up rate, data clean deadlines, protocol compliance , and enrollment. * Lead study meetings to ensure...experience. * Minimum 8 years of clinical research experience, medical device experience preferred. This should includes… more
    Teleflex (11/20/25)
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  • Senior Manager, Customer Excellence

    Stryker (Denver, CO)
    …Bachelor's degree * 10+ years of work experience required * 7+ years medical device or marketing/sales experience preferred * Experience developing strategic ... working with Surgeons, KOL or Clinical influencers **Preferred** + 5+ year in sales or medical education in the medical device industry + People leadership… more
    Stryker (11/19/25)
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  • Senior Manager, Engineering

    Bausch + Lomb (Tampa, FL)
    …FDA, EMA, etc.) and applicable testing methods for use in pharmaceutical and medical device applications. + Support the commercial packaging operations at ... + 10+ years of relevant packaging experience in a regulated pharmaceutical or medical device industry and with minimum 3 yrs management experience (or… more
    Bausch + Lomb (12/23/25)
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  • Sr. Clinical Trial Manager

    Actalent (Menlo Park, CA)
    …in a Clinical Operations study lead role, at a sponsor company (pharma, biotech, or medical device ) with a strong track record of successful trial initiation and ... experience within in vitro diagnostics (IVD) highly preferred; pharmaceutical, biologics or medical device experience also acceptable . Thorough knowledge of… more
    Actalent (12/13/25)
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  • Quality Engineer

    DEKA Research & Development (Manchester, NH)
    …for a Quality Engineer to work in the Quality Department in a dynamic Medical Device Research and Development environment. The position reports to the Quality ... a Quality Engineer to provide Quality guidance in a dynamic, fast-paced medical device research, development, and manufacturing and distribution environment. How… more
    DEKA Research & Development (12/12/25)
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  • Engineering Manager, Advanced Operations

    Stryker (Mahwah, NJ)
    …standards. + Identify and implement NPI best practices across programs. **Med Device Compliance :** + Lead cross-functional teams in launching new technologies ... experience + Proven new product introduction experience in a regulated industry ( medical device preferred) + Strong knowledge of DFM, process validation,… more
    Stryker (12/09/25)
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  • Manufacturing Engineer

    Kelly Services (Madison, WI)
    …and electrical manufacturing processes, including assembly and testing + Experience in medical device manufacturing + Experience leading project teams or ... **Madison, Wisconsin** **Pay start at $45/hr W2 (+/- DOE)** **Enhanced benefits ( medical , dental, vision) + Paid Vacation** **Summary:** This description covers the… more
    Kelly Services (12/04/25)
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  • Tool Engineer- INDIA

    Insight Global (Westborough, MA)
    …platforms used throughout the software development lifecycle (SDLC) of Software as a Medical Device (SaMD). This includes tools such as Jama Connect ... communication, problem-solving, and documentation skills. * Experience supporting tools in a medical device or health-tech environment. * Familiarity with test… more
    Insight Global (11/12/25)
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  • Clinical Affairs Manager, Interventional Access…

    Teleflex (Houston, TX)
    …clinical exposure in the medical field in the Cardiology environment. * Medical Device industry supporting Clinical and Medical Affairs, strongly ... compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements… more
    Teleflex (12/13/25)
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