- Cordis (Miami Lakes, FL)
- …**Required Qualifications:** + 15+ years of experience in medical education, clinical affairs , or medical affairs with 6+ years of experience in ... launches. + Operate cross-functionally with Commercial, Marketing, R&D, Clinical Affairs , Regulatory , and Quality to align messaging... medical education leadership within the medical device industry, with significant exposure to… more
- BioFire Diagnostics, LLC. (Salt Lake City, UT)
- …broader quality goals and regulatory landscapes. + Deep understanding of global medical device /IVD regulations (eg, FDA 803/806, MEDDEV, QSR 820, ISO 13485) ... Fields) with 6 years of experience in a regulated medical device /IVD industry employment position such as...industry employment position such as post-market surveillance, quality assurance, regulatory affairs , clinical affairs or… more
- BD (Becton, Dickinson and Company) (Salt Lake City, UT)
- …and new product development through the application of Quality engineering skills for medical devices . This person will handle projects and tasks, from product ... evaluate effectiveness of GMPs and established Quality Systems + ** Regulatory Support:** Assist Regulatory Affairs ...Management and Change Controls is required. + Experience in medical device industry is required. + American… more
- Genentech (South San Francisco, CA)
- …early and late stage research and development of pharmaceutical products, digital health, and medical devices . As a member of the R&D Law Group, this **"Senior ... support Research and Early Development, Clinical Operations, Global Product Development, and Medical Affairs functions by providing strategic legal advice to… more
- Hologic (Newark, DE)
- …Are you passionate about driving innovation while ensuring compliance and quality in medical device development? At Hologic, we are seeking a **Lead Design ... and a commitment to delivering safe, reliable, and durable medical devices , we want to hear from...+ Collaborative and team-oriented, building strong relationships across R&D, Regulatory Affairs , Manufacturing, and other key stakeholders.… more
- West Pharmaceutical Services (Williamsport, PA)
- …Skills and Abilities** + ** Regulatory Skills:** In-depth knowledge of medical device and pharmaceutical regulations and guidelines, including cGMP, ICH ... and manages quality control, quality assurance, quality systems, metrology and/or regulatory affairs , personnel, department resources, and continuous improvement… more
- Cook Medical (Bloomington, IN)
- Overview The Packaging Engineer 2 uses their experienced in medical device packaging to design and develop solutions for new and modified products. This includes ... packaging activities with a cross-functional team including SBU Product Management, Regulatory Affairs , Operations, Quality Assurance, Clinical Affairs ,… 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...and Clinical Training Managers, Sales, Field clinical, Marketing, and Medical Affairs to ensure training curriculum and… more
- Hologic (Marlborough, MA)
- …and requirements traceability. + Familiarity with Good Laboratory Practices and global regulatory requirements for medical devices . + Proficiency in ... in ensuring the safety, reliability, and compliance of life-changing medical devices ? At Hologic, we are seeking...a subject matter expert, you will partner with R&D, Regulatory Affairs , and Manufacturing Engineering teams to… more
- Zimmer Biomet (Englewood, CO)
- …with respect to medical device development. + Understanding of medical device industry regulatory requirements required. + Proficient with CAD. ... Paragon 28, a Zimmer Biomet Company focusing on orthopedic medical devices for the foot and ankle....with 6+ years of experience + Prior experience in medical device development required. + Prior experience… more