- System One (Mahwah, NJ)
- …Engineer Location: Mahwah, NJ Compensation: $53.00- $70.00 Type: Contract Overview Global Medical Device company looking for experienced Engineer to join their ... up to and including that necessary to support a regulatory submission. Requirements + A minimum of BS degree...analysis and familiarity with Minitab and/or MS Excel. + Medical device or similar regulated industry experience… more
- J&J Family of Companies (New Brunswick, NJ)
- …meta-analyses + Evaluate the relevance and reliability of new data sources for medical device studies, including product-specific studies of J&J devices + ... and epidemiologic research to support post-market safety and effectiveness, regulatory submissions, product development, product launches, value assessments, predictive… more
- 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
- Robert Half Technology (Mahwah, NJ)
- …the efficiency and effectiveness of documentation systems. * Support compliance with medical device regulations and quality assurance standards. * Collaborate ... play a crucial part in managing document-related changes while ensuring compliance with regulatory standards for medical devices. This is a long-term contract… 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
- 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
- Cardinal Health (Trenton, NJ)
- …will also help to support inorganic product opportunities and better define our medical device connectivity strategy. **_Responsibilities_** + Support and be a ... equivalent work experience, preferred. + 4+ years experience in related field, preferred. + Medical device or global medical products experience preferred +… more
- Church & Dwight Co., Inc. (Princeton, NJ)
- …record + Transitioning to Generalist in at least 1 area: Consumer products, medical device , food, dietary supplements or pharmaceutical + Contributions focused ... ensures all applicable regulations & standards across all 15 Power Brands, in Medical Devices, Drug / Homeopathics, Food / Feed / Specialty Products Division (SPD),… more
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