- J&J Family of Companies (Santa Clara, CA)
- …Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... engineering discipline and 3+ years of relevant experience + Experience in the medical device industry is strongly preferred + Strong understanding of cGMP,… more
- West Pharmaceutical Services (Williamsport, PA)
- …preferred **Work Experience** + 10+ Years of job-related experience required in the Medical Device or Pharmaceutical Industry. + 8+ Years of supervisory ... Senior Quality Manager Requisition ID: 71560 Date: Nov 26,...an FDA or ISO regulated industry required, preferably in medical device manufacturing. **Preferred Knowledge, Skills and… more
- Stryker (San Jose, CA)
- … (SaMD)/Software in a Medical Device (SiMD) and non- medical device software to support projects as a quality engineer for post-market activities to ... Quality Engineer, Post Market** to support our Medical 's Digital Health division and portfolio Software as a...visualization and monitoring. + Exposure to Software as a Medical Device (SaMD), Software in a … more
- Terumo Medical Corporation (Elkton, MD)
- …mathematics, and statistics skills + Demonstrated working knowledge of key medical device related standards including 21 CFR 820 ( Quality Systems Medical ... Req ID: 5357 Location: Elkton, MD, US Company: Terumo Medical Corporation Department: TIS Design Assurance/ Quality Engineering...scientific environment + Minimum of 2 years of experience in a regulated industry ( medical device industry… more
- Aerotek (Minneapolis, MN)
- ** Quality Inspector - Medical Device Manufacturing** **About the Role** Join our team as a ** Quality Inspector** and play a key role in ensuring the ... safety and reliability of life‑changing medical devices. You'll work in a fast‑paced, collaborative environment...vision systems, you'll help maintain the highest standards of quality and compliance across our production process. **Why You'll… more
- Stryker (Portage, MI)
- …Assurance** to support our Medical 's Digital Health division and portfolio Software as a Medical Device (SaMD) or Software in a Medical Device (SiMD) ... maintained engineering documentation, including Design History Files, in accordance with medical device regulatory standards. + Demonstrated strong understanding… more
- J&J Family of Companies (Danvers, MA)
- …verification and validation plan and strategies while maintaining traceability. + Use Software as a Medical Device (SaMD) and Software in a Medical Device ... health for humanity. Learn more at https://www.jnj.com **Job Function:** Quality **Job Sub** **Function:** R&D/Scientific Quality **Job...of 5 years of related work experience within the medical device industry on SaMD and SiMD… more
- Integra LifeSciences (Plainsboro, NJ)
- …Certifications: ASQ CQE preferred + Experience: 6 to 8 years of experience in a Quality Assurance role for medical device or pharmaceutical manufacturing. + ... corporate policies, US Food and Drug Administration regulations, ISO 9001, ISO 13485, the Medical Device Directive, the Canadian Medical Device … more
- Cook Medical (Bloomington, IN)
- …clinical, and regulatory affairs.- Provide leadership in the understanding of medical device regulations and best practices.- Manage conflict resolution ... Overview The Quality Engineer serves as the lead quality...degree and 5-8 years of experience- Demonstrates knowledge of medical device regulation (ISO 13485, 21CFR) and… more
- Stryker (San Jose, CA)
- … Engineer** to support our Medical 's Digital Health division and portfolio Software as a Medical Device (SiMD) or Software in a Medical Device (SiMD) ... strong technical skills + Experience with regulatory agencies (FDA, MoH, TUV) and medical device regulations (820, IEC 62304/82304, 60601), with experience in… more