- Meta (New York, NY)
- …a scientific discipline or equivalent work experience 6. 3+ years of industry experience in medical device regulatory affairs or related industry 7. ... regulatory affairs specialist to join our medical devices compliance team. You will get...get to work on wearables and Software as a Medical Device (SaMD) applications for the US… more
- Haleon (Warren, NJ)
- …legislation covering pharmaceuticals, medical devices , cosmetics and foods. The Regulatory Affairs team helps to guide our company on our responsibility ... us achieve this goal. Right now, we're looking for a Co-Op student in US Regulatory Affairs to join us to do career defining work. **A career in Regulatory … more
- embecta (Parsippany, NJ)
- …discipline (eg engineering, bioengineering, biology, chemistry). + 5+ years Regulatory Affairs experience in medical device companies. + Must have ... in both the US and Europe, and related regulatory affairs activities to ensure compliance with...current knowledge of the US and European Medical Device regulations. + Demonstrated success in… more
- AbbVie (Branchburg, NJ)
- …RDQA) organization, working collaboratively and strategically with colleagues in R&D, Operations, Regulatory Affairs , Medical Safety and more to develop ... and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description As a Medical Device & Combination Product Quality Intern...procedures. We support the development of a variety of medical devices in the Aesthetics space, including… more
- Kelly Services (Raritan, NJ)
- …Supports creation of project value propositions as needed. + Provides strong connectivity with Medical Affairs , R&D, Regulatory Affairs , and Clinical ... communication skills across different organization levels **Preferred:** + Prior experience in medical devices or other regulated industry + Knowledge of… more
- Bristol Myers Squibb (Princeton, NJ)
- …or Madison, New Jersey **Position Summary** The Director of Early Precision Medicine Regulatory Affairs leads global regulatory strategy for biomarkers and ... background, PhD., MD, PharmD, MS **Experience Requirements:** Significant experience in regulatory affairs and diagnostic-related development eg, >8-10 years.… more
- Sanofi Group (Morristown, NJ)
- …framework, providing expert guidance on Chemistry, Manufacturing, and Controls (CMC) and medical device regulatory requirements across the product lifecycle. ... we chase the miracles of science to improve people's lives. The Global Regulatory Affairs (GRA) CMC & Device Organization within Sanofi R&D serves as… more
- United Therapeutics (Trenton, NJ)
- …or pharma regulatory experience with a Bachelor's Degree in life sciences, quality, regulatory affairs or a related area of study or 10+ years of biologic ... ( **miroliver(R)** ), and a bioengineered external liver assist device for acute liver failure ( **miroliver** **_ELAP_** **(R)**...experience with a Master's Degree in life sciences, quality, regulatory affairs or a related area of… more
- Sanofi Group (Morristown, NJ)
- …(3+ years preferred) of regulatory experience, preferably within the pharmaceutical/ medical device /biotech industry + Knowledge and understanding of complex ... **Job Title:** Associate Director, Global Regulatory Affairs Advertising and Promotion **Location**...R&D colleagues, as well as other stakeholders (eg, Legal, Medical , Marketing, Communications and Compliance). + Participates in the… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Global Medical Affairs Director - Oncology **Location:** Cambridge, MA / Morristown, NJ **About the job** **About us:** In order to pursue ... miracles of science to improve people's lives", Specialty Care Medical Affairs have a vision to be...engagement. We serve as key strategic partners for commercial, regulatory , R&D, market access and external affairs … more
- Sanofi Group (Morristown, NJ)
- …strategic partner within Sanofi's regulatory framework, providing expert guidance on medical device regulatory requirements across the product lifecycle. ... critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team...cross-functional teams + Develop and execute innovative and sustainable medical device regulatory strategies covering… more
- Sanofi Group (Morristown, NJ)
- …(early phase, late stage and marketed products). + Develop innovative and sustainable medical device regulatory strategies covering combination products and ... team is part of the Global Regulatory Affairs , Regulatory CMC and Device ...to internal regulatory processes and procedures for medical devices and combination products. + Engage… more
- Sanofi Group (Morristown, NJ)
- …strategic partner within Sanofi's regulatory framework, providing expert guidance on medical device regulatory requirements across the product lifecycle. ... critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team...cross-functional teams. + Develop and execute innovative and sustainable medical device regulatory strategies covering… more
- Fujifilm (Trenton, NJ)
- …**Job Description** **Responsibilities** + Manage and support the day-to-day legal affairs of assigned Medical Device businesses or ... The Senior Counsel, reporting to the Division General Counsel, Medical Devices , will be an experienced commercial...Counsel and senior business management on general legal and regulatory risks affecting the Medical Device… more
- Sanofi Group (Morristown, NJ)
- …strategic partner within Sanofi's regulatory framework, providing expert guidance on medical device regulatory requirements across the product lifecycle. ... critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team...teams. + Contribute to and execute innovative and sustainable medical device regulatory strategies covering… more
- Terumo Medical Corporation (Somerset, NJ)
- …product and scientific support for the organization that includes Medical Affairs , Clinical Operations, Sales, Marketing, Regulatory Affairs , to ensure ... therapeutic area, provide support in the following ways: + Medical affairs strategy: + Contribute to the...+ Regulatory activities partnership: + Work with regulatory affairs to ensure that all written… more
- Grifols Shared Services North America, Inc (New Brunswick, NJ)
- …regulatory strategies for projects and issues affecting development of new products or medical devices or new indications for existing products + Provides ... staff + May have responsibility for maintaining a compliant medical device quality system for R&D and...years of experience in positions of increasing responsibility within Regulatory Affairs or related field within the… 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
- Organon & Co. (Jersey City, NJ)
- …Position** Leading the Regulatory Policy and Intelligence activities for Global Regulatory Affairs covering all Therapeutic Areas and products, as well as ... of the world of interest to Organon. **Responsibilities** + Provide Global Regulatory Policy and Intelligence insights to the organization to guide product… more
- Insight Global (New York, NY)
- …Skills and Requirements -2+ years of experience working in regulatory affairs (especially product registration) -Experience within cosmetic, ... large CPG client of ours is looking for a regulatory coordinator for a 5 month (starting) contract that...CPG, pharma, or medical device industries -BS Degree in Scientific… more