• Staff Electrical Engineer

    TE Connectivity (Wilsonville, OR)
    … business unit is a leader in engineering design and manufacturing within the medical device industry. Specializing in critical components such as metal shafts, ... design specifications, test plans and qualification reports. Ensure compliance with relevant medical device regulations and quality processes. * Mentorship: Act… more
    TE Connectivity (07/26/25)
    - Related Jobs
  • Senior Attorney, Litigation

    Cook Medical (Bloomington, IN)
    …firm developing and driving strategy for complex litigation* Experience working within medical device , pharma, healthcare, or other highly regulated industry* JD ... Abilities* Excellent understanding of regulatory environment and legal frameworks within the medical device industry, in addition to all applicable ethics and… more
    Cook Medical (09/05/25)
    - Related Jobs
  • Manufacturing Engineering Team Lead

    ZOLL Medical Corporation (Pawtucket, RI)
    …Six Sigma Green Belt or equivalent problem-solving expertise preferred + Experience in medical device or other regulated industry preferred + Detailed knowledge ... structure and documentation methods. + Understanding of process validation and qualification in medical device + Proficient in PC applications (MS Office, Visio)… more
    ZOLL Medical Corporation (08/11/25)
    - Related Jobs
  • Sr Supply Chain Planner

    Terumo Medical Corporation (Somerset, NJ)
    …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... 13, 2025 Req ID: 4841 Location: Somerset, NJ, US, 08873 Company: Terumo Medical Corporation Department: TMC S&OP Global Terumo Medical Corporation (TMC)… more
    Terumo Medical Corporation (07/09/25)
    - Related Jobs
  • Senior Aortic Clinical Specialist

    Medtronic (Wichita, KS)
    …experience coordinating programs + Thorough working knowledge of medical terminology, medical proceduresand the medical device industry + Excellent ... Aortic product IFUs for safe and effective use of devices. + Develop and maintain comprehensive clinical and technical product knowledge. + Understand… more
    Medtronic (09/12/25)
    - Related Jobs
  • Biocompatibility & Toxicology Senior Scientist

    DEKA Research & Development (Manchester, NH)
    …for a Biocompatibility & Toxicology Senior Scientist to join our team focused on medical device and combination product development. The individual in this ... other communications as needed to support program objectives + Develop and deploy mechanisms to continually maintain state of...Minimum of 7 years direct work experience in a medical device and/or combination product more
    DEKA Research & Development (07/18/25)
    - Related Jobs
  • LimFlow Account Manager - Northern California,…

    Stryker (San Jose, CA)
    …or 6 years demonstrated successful sales experience. + Minimum 5 years of medical device industry experience selling physician preference therapies in the ... setting for the PAD/CLTI Patient. + Demonstrated ability to effectively establish new medical device therapies . + Experience in peripheral arterial and/or… more
    Stryker (09/10/25)
    - Related Jobs
  • Project Manager, R&D

    ZOLL Medical Corporation (Chelmsford, MA)
    …years of experience as an engineer developing products, preferably in the medical device industry required + Project Management Professional (PMP) certification ... innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and… more
    ZOLL Medical Corporation (08/15/25)
    - Related Jobs
  • Staff Quality Engineer II - Post Market…

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …critical role ensuring product safety and compliance in the medical device industry. **Responsibilities** + **Lead Post-Market Surveillance Activities:** ... quality and safety **Skills** + **Regulatory Knowledge:** Extensive understanding of FDA medical device regulations (21 CFR Part 820), ISO standards (13485,… more
    BD (Becton, Dickinson and Company) (08/27/25)
    - Related Jobs
  • Sr. Director - Global Regulatory Lead…

    Lilly (Indianapolis, IN)
    …team members to develop a global regulatory strategy which supports product (including delivery device and relevant medical devices) development, ... is to develop and implement innovative global regulatory strategies for product (s) in the assigned therapeutic area. The GRL is the accountable decision maker… more
    Lilly (09/02/25)
    - Related Jobs