- J&J Family of Companies (Chicago, IL)
- …and profoundly impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Medical Affairs Group **Job Sub** **Function:** Medical ... (CAS) partners with Level 2 or 3 CAS and Medical Affairs to learn training and certification...learn training and certification criteria for J&J Vision (JJV) Medical Devices . This includes our Refractive Laser… more
- Guidehouse (Mclean, VA)
- …FDA/ICH guidelines and CDISC data standards + Experience in pharmaceutical industry regulatory affairs and/or quality assurance and/or quality control + Direct ... market research and technical evaluation panels. You'll also advise on clinical, regulatory , and manufacturing aspects of medical product development, ensuring… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …+ Minimum of two (2) or more years experience in clinical research, with medical device and/or pharmaceutical trials. + Strong computer skills with proficiency ... domestically up to 10%. **Preferred:** + Previous experience with medical device trials **Why join Olympus?** We...local law. Posting Notes: || United States (US) || Pennsylvania (US-PA) || Center Valley || Medical Affairs… more
- Globus Medical, Inc. (Audubon, PA)
- …technique guides, brochures and other marketing/sales support materials + Partnering with Regulatory Affairs in planning, coordination, writing, and execution of ... role, you must possess the following:** + 8+ years' experience in the medical device product development and research field; 5+ years of people and or program… more
- Actalent (Irvine, CA)
- …will play a crucial role in ensuring the quality and compliance of new medical device products throughout their development lifecycle. You will be responsible ... plans and conducting risk reviews. Essential Skills + Experience with the medical device product development lifecycle, including risk management and… more
- Abbott (Atlanta, GA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... Minimum 5 years of project management experience, preferably in a medical device manufacturing, engineering, or quality-focused environment. **Preferred… more
- BD (Becton, Dickinson and Company) (Sparks, MD)
- …methods is required. Familiarity with Design Control requirements and knowledge of Medical Device Validations is preferred. **Education and Experience:** + ... Bachelor's degree. Typical degrees in Biological Sciences, Chemistry, and/or Regulatory Affairs . Other fields can be considered with the appropriate experience… more
- Dentsply Sirona (Lancaster, PA)
- …solutions offering including dental and oral health products as well as other consumable medical devices under a strong portfolio of world class brands. Dentsply ... required. + Associate's or Bachelor's degree in Quality Assurance, Regulatory Affairs , or a related field is... roles within a regulated manufacturing environment preferred. + Medical device industry experience is a plus.… more
- Zimmer Biomet (Englewood, CO)
- … device from ideation to commercialization required. * Understanding of medical device industry regulatory requirements preferred. * Experience with ... meaningful projects that focus on design and development of medical devices and development life cycle with...engineering discipline with 3-7 years of development experience in medical device . * Prior experience in taking… more
- Hologic (Newark, DE)
- …leading major US and global clinical trials across multiple phases of medical device development. You'll ensure studies are executed on-time, on-budget, ... the highest quality. Collaborate with top talent across Clinical Development, R&D, Regulatory Affairs , Program Management, Legal, Marketing, and Operations to… more