• Biocompatibility Manager - Medical Devices…

    Abbott (St. Paul, MN)
    …ISO 10993 standards, biomaterials, toxicological assessment, extractable and leachable analysis, medical device manufacturing processes, and biocompatibility ... such as ISO 10993. Additionally, this role requires knowledge of the medical device biocompatibility discipline throughout the product lifecycle and knowledge… more
    Abbott (04/08/25)
    - Related Jobs
  • COOK Medical Fall 2025 R&D Engineering…

    Cook Medical (Bloomington, IN)
    …each position provide s real-world experience with meaningful projects in the medical device manufacturing industry. Responsibilities - Utilize engineering ... knowledge to p roduce project deliverables / documents - Adhere to the Quality Management System (QMS) and its processes to meet FDA 21 CFR 820, ISO 13485, and other applicable regulatory requirements - Must maintain all training requirements for the position,… more
    Cook Medical (04/02/25)
    - Related Jobs
  • Sr. Automation Design Engineer

    TE Connectivity (Plymouth, MN)
    …Integration (Primary) + Stay abreast of emerging technologies and industry trends in medical device manufacturing . + Propose and implement innovative ... of FDA regulations, ISO standards, OSHA standards and GMP requirements for medical device manufacturing . + Proven expertise in process development, equipment… more
    TE Connectivity (04/11/25)
    - Related Jobs
  • Senior Manager, Quality - Combination Products,…

    Gilead Sciences, Inc. (La Verne, CA)
    …relevant experience with a Master's degree in a Science or Engineering field + Medical device manufacturing , testing or QA experience is essential. ... provides comprehensive support of these combination products. **Roles/Responsibilities:** + Monitor medical device standards for quality management system (QMS)… more
    Gilead Sciences, Inc. (04/28/25)
    - Related Jobs
  • UL - Quality Systems Engineer

    Ultralife Corporation (Newark, NY)
    …of quality systems, process controls and continuous improvement methodologies; electronics and medical device manufacturing preferred + Knowledge and working ... to successful transition to production. Education and Experience: + Proven record of experience in the medical device industry in development and implementation… more
    Ultralife Corporation (05/26/25)
    - Related Jobs
  • Production Supervisor - First Shift, Selution

    Cordis (Irvine, CA)
    …experience supervising in a highly regulated manufacturing environment is required. Medical device manufacturing experience is highly preferred. + ... **Overview** Cordis is a pioneering medical technology company specializing in groundbreaking solutions for cardiovascular and peripheral vascular diseases. Our… more
    Cordis (04/09/25)
    - Related Jobs
  • Staff Operations Quality Engineer

    Caris Life Sciences (Phoenix, AZ)
    …Quality Assurance or related functional area preferably in the IVD or medical device manufacturing environment or CLIA/CAP/LDT/clinical laboratory ... ( Manufacturing ) Operations. Support the creation of DMR and DHR for new medical device /IVD products. + Risk Assessment: Partner with Risk Management team to… more
    Caris Life Sciences (04/04/25)
    - Related Jobs
  • Production Operator 2

    Teleflex (Chelmsford, MA)
    …/ Experience Requirements** + High School Diploma or equivalent strongly preferred + Prior medical device manufacturing experience preferred. + Must be able ... make a difference in patients' lives. **Position Summary** To manufacture/test medical device assemblies (including all lower-level sub-assemblies and… more
    Teleflex (05/30/25)
    - Related Jobs
  • Enterprise Excellence Manager

    Teleflex (Chelmsford, MA)
    …Chelmsford site exemplifies best-in-class operational excellence within a regulated medical device manufacturing environment. **Principal Responsibilities** ... large-scale change programs in a multi-site or global setting. * Experience in medical device manufacturing or a regulated industry is highly desirable. *… more
    Teleflex (05/08/25)
    - Related Jobs
  • Senior Validation Engineer

    Actalent (Lakewood, CO)
    …Engineer will play a crucial role in validating multiple systems within a medical device manufacturing environment. This individual will be responsible ... test and measurement methods. Responsibilities + Validate multiple systems in a medical device manufacturing environment. + Execute a validation Master Plan,… more
    Actalent (05/30/25)
    - Related Jobs