- University of Southern California (Los Angeles, CA)
- …wealth of professional experience in regulatory sciences involving drugs and/or medical devices . These real-life lessons brought to the classroom and ... education or research in the areas of drug and device development and regulatory considerations. Specific areas...expertise within a professional or academic career related to regulatory affairs or sciences is suitable. The… more
- Philips (Washington, DC)
- …a minimum of 10+ years' experience in FDA Regulations, Global Regulatory Affairs , Policies and Standards within the Medical Device /Technology industry or ... The Regulatory Science & Policy Director is responsible for...Director is responsible for guiding the analysis of global regulatory requirements, policies and industry standards to identify their… more
- Takeda Pharmaceuticals (Boston, MA)
- …represented at the Labeling cross functional teams including clinical, safety, medical affairs , and commercial, to ensure highly effective communication ... life-changing therapies to patients worldwide. Join Takeda as Senior Manager, Global Regulatory Labeling Strategy where you will be responsible for the development… more
- Takeda Pharmaceuticals (Boston, MA)
- …represented at the Labeling cross functional teams, including clinical, safety, medical affairs , and commercial, to ensure unparalleled communication ... bring life-changing therapies to patients worldwide. Join Takeda as Director, Global Regulatory Labeling Strategy where you will be responsible for the development… more
- Danaher Corporation (New York, NY)
- … regulatory , market access, and post-market). You'll collaborate with clinical, regulatory /quality, R&D, medical affairs , IT/security, and our Operating ... and visualization tools. + Proven experience analyzing RWE/RWD (EHR, claims, registries, device logs) for clinical, regulatory , or market access impact. Travel,… more
- Actalent (Santa Clara, CA)
- …+ 2-3 years of experience in complaint handling, quality assurance, or regulatory affairs within the medical device or pharmaceutical industry. + Strong ... such as R&D, Manufacturing, and Regulatory . The position requires determining regulatory reportability and submitting Medical Device Reports (MDRs) to… more
- Abbott (Pleasanton, CA)
- …from varied disciplines including Clinical Medicine, Engineering, Marketing and Regulatory Affairs required. + Medical device industry experience. + ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
- Abbott (Princeton, NJ)
- …**Familiarity and experience working across functions (eg, Operations/Supply Chain, Quality, Regulatory Affairs , Market Access, Medical Affairs ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
- J&J Family of Companies (Irvine, CA)
- …and profoundly impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Medical Affairs Group **Job Sub** **Function:** Medical ... Structural Heart** . **Role Purpose** The Director will have medical affairs responsibility in providing therapeutic and...and clinical expertise in support of the development of medical devices for the treatment of structural… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …analysis in collaboration with cross-functional teams such as Marketing, Operations, Finance, Regulatory Affairs , Quality Assurance, Medical & Scientific ... or franchises through strong collaboration with sales, marketing, operations, finance, regulatory affairs , quality assurance, medical /scientific affairs… more