- embecta (Parsippany, NJ)
- …pragmatic solutions. The ideal candidate will have commercial legal experience in the medical device , pharma or healthcare industry supporting the US and/or ... to practice in at least one state. + 5+ years of experience, preferably within medical device , pharma or healthcare industries. + Thorough knowledge of the False… more
- Fresenius Medical Center (Kenilworth, NJ)
- …service philosophy. Adheres to the FMCNA Compliance Program including following all regulatory and FMS policy requirements. Functions as part of the hemodialysis ... 5 feet. There is a two-person assist program and material assist devices for the heavier items. **EDUCATION** + Center for Medicaid/Medicare Services (CMS)-approved… more
- Integra LifeSciences (Princeton, NJ)
- …mindset, a willingness to learn about sterilization and microbiology, an understanding of medical device quality systems, and a commitment to ensuring product ... related discipline, with 5+ years of experience in Quality Assurance role for medical device or pharmaceutical manufacturing, or equivalent education and years… more
- J&J Family of Companies (Raritan, NJ)
- …labeling implementation inputs and deliverables for registration sample packs, Software as a Medical Device (SaMD), and other non-U.S. labeling in scope of GL. ... impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Regulatory Affairs Group **Job Sub** **Function:** Regulatory Product Submissions… more
- Stryker (Mahwah, NJ)
- …the Technical Publications Specialist, you will play a key role in ensuring our medical device labeling is clear, compliant, and accessible, supporting safe and ... teams and external partners to deliver high-quality documentation that meets global regulatory standards and enhances patient safety. To learn more about Stryker's… more
- System One (Park Ridge, NJ)
- …directly impact product safety, regulatory success, and speed-to-market for critical medical devices and healthcare products. As a recognized authority, you ... technical direction, leading high-impact sterilization programs, and ensuring full regulatory compliance across the product lifecycle-from development through commercialization.… more
- Sokol Materials & Services (Skillman, NJ)
- …experience in CQV and/or CSV within the pharmaceutical, biotechnology, cell therapy or medical device industries. + Experience with Cell Therapy equipment (cell ... and methodologies, including risk-based validation approaches. + Knowledge of regulatory requirements, including FDA, EMA, and ICH guidelines. Knowledge, Skills… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …+ Sound knowledge of material science and engineering principles + Working experience in medical device industry + Familiar with design control process and ... program success by working cross functionally with R&D-Engineering, Marketing, Medical Affairs, Manufacturing, Quality and Regulatory Affairs....medical device regulations + Knowledge of method… more
- Integra LifeSciences (Plainsboro, NJ)
- …European Medical Device Directives, Canadian Medical Device Regulations, and other applicable regulatory agencies. Experience with assessing quality ... System Documentation to ensure that the development, manufacture and distribution of medical products are in compliance with company policies and procedures, US.… more
- Sokol Materials & Services (Skillman, NJ)
- …Minimum of 7 years of CQV experience in pharmaceutical, biotechnology, cell therapy, or medical device industries, with at least 5 years focused on utilities and ... qualification. + Strong understanding of validation principles, methodologies, and regulatory requirements, including FDA, EMA, and ICH guidelines. Knowledge, Skills… more