- Abbott (Alameda, CA)
- …+ Work closely with in-country regulatory representatives, compile, prepare, and review medical device or IVD submissions to regulatory agencies in the ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
- Amgen (Washington, DC)
- …these qualifications. **Basic Qualifications:** Doctorate degree and 2 years of Medical Device , Pharmaceuticals or Biotechnology experience Or Master's degree ... Lead a team of quality professionals overseeing external mechanical device suppliers + Ensure compliance with scientific, regulatory...and 6 years of Medical Device , Pharmaceuticals or Biotechnology experience Or… more
- Medtronic (Fridley, MN)
- …as well as the progression from manual submission towards automated submission between medical device companies and regulatory bodies. + Familiar with ... respect to product changes requiring updated GTS licensing. + Experience with medical device product development to ensure that regulatory issues are… more
- Lilly (Indianapolis, IN)
- …development. **Additional Preferences and Information:** + Knowledge of cGMP requirements in medical device manufacturing, highly preferred. + Experience in ... As the Associate Director of Technical Services/Manufacturing Science (TS/MS) in the Device and Packaging Network, you will lead the charge in ensuring operational… more
- Element Materials Technology (Fairfield, OH)
- …across a variety of implants and devices . This position will support our clients' medical device testing requirements and work with medical device ... **Overview** Element has an opportunity for an *on-site* ** Medical Device Project Engineer** to join our rapidly expanding team in Fairfield, Ohio. This position… more
- Tecomet (Manchester, NH)
- …in quality assurance and regulatory affairs within a regulated industry ( medical devices preferred); **WORK ENVIRONMENT / PHYSICAL DEMANDS:** + Typical ... **POSITION SUMMARY:** The Quality Assurance & Regulatory Affairs Manager oversees the quality management system...a related field, or equivalent work experience in the medical device industry; + 5+ years of… more
- Xylem (Chaska, MN)
- …in a Science or Engineering field, or equivalent work experience * 5+ years of Medical Device Regulatory Affairs experience, domestic and international * 3 ... Product Compliance Analyst** is focused on product compliance to regulatory requirements for medical devices ...activities as well as other deliverables as related to medical device projects * Review and approve… more
- Abbott (Maple Grove, MN)
- …space_ + 10+ years of cyber security experience and expertise + Experience with medical device security and regulatory requirements as they relate connected ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
- Terumo Medical Corporation (Somerset, NJ)
- …(TMC) develops, manufactures, and markets a complete, solutions-based portfolio of high-quality medical devices used in a broad range of applications for ... of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in...media planning and collateral creation. + Ongoing collaboration with medical , regulatory and legal partners to assure… more
- Lilly (Indianapolis, IN)
- …Management skills + Familiarity and practical experience with medical device / combination product quality & regulatory requirements, including GMP/CFR, ... will provide leadership for Commercialization Global Program Managers (GPM's) who lead medical device and drug/ device combination product commercialization… more