- Organon & Co. (Jersey City, NJ)
- …of global GMP Quality Systems and regulatory requirements. + Experience in medical device Quality Systems is preferred, including familiarity with ... responsible for ensuring that all Organon products managed by External Quality Assurance (EQA) are manufactured, packaged, analyzed, released, stored, and… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …education and experience. + Preferred minimum of ten-to-fifteen years of experience in the medical device industry, with at least nine years in a regulatory ... **maker of possible** with us. The Regulatory Affairs (RA) Director is responsible for the management and setting the...legal); and negotiate with Regulators. + Ability to interpret medical device testing methods and statistics, as… more
- J&J Family of Companies (Raritan, NJ)
- …field is highly desirable. + Comprehensive understanding of the medical device supply chain, operations, manufacturing, and quality assurance within the ... Stay updated on industry trends, emerging technologies, and regulatory changes impacting the medical device sector. + Provide strategic updates and insights to… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …+ Minimum 8 years of regulatory affairs experience within the pharmaceutical or medical device industries, ideally with expertise in drug- device combination ... **Job Description Summary** As Associate Director , Regulatory Affairs, you will be responsible for...strong and respected voice. + Comprehensive knowledge of US medical device regulations (FDA), Clinical Practice standards,… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …complementary technology experience + Experience delivering technology solutions in a Medical Device or Pharmaceutical regulated environment + Solid knowledge ... Business Partner will report to the TGS Senior Director , Product Services and work with the Quality...of possible** BD is one of the largest global medical technology companies in the world. Advancing the world… more
- AbbVie (Florham Park, NJ)
- …position is responsible for the operations and strategic design of the US Medical Device & Aesthetics businesses global supply planning organization which ... support very significant revenue streams for Medical Device & Aesthetics businesses. Achieving the revenue goals are critical to AbbVie's top line revenue goals… more
- Bausch + Lomb (Trenton, NJ)
- …R&D/Project Management, Clinical/ Medical Affairs, Biometrics, Regulatory Affairs, Quality Assurance, Pharmacovigilance/GPSS and Drug/ Device Safety, and ... areas to provide input on study-related documents and issues (DMP, SAP, drug/ device supplies, CSR, etc.). + Provides clinical operations input in the identification,… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …field required; _Master's degree preferred_ + Expert-level proficiency in ISO 13485, Medical Device Regulation (MDR), and FDA requirements with demonstrated ... **Job Description Summary** As Associate Director of Technical Solutions at BD Pharmaceutical Systems,...GMP/GDP protocols, and USP-EP guidelines as they apply to medical device environments + Demonstrated capability to… more
- Merck (Rahway, NJ)
- …distribution/ transportation technologies for pharmaceutical products including parenteral and/or medical device and combination products. + Demonstrated ... **Job Description** Director , Packaging Shipping Systems (Logistics and Distribution Technology)...stakeholders to ensure that all platforms meet safety, efficacy, quality , and robust supply standards. + Develop and maintain… more
- NBC Universal (Englewood Cliffs, NJ)
- …to be completed during 2025. We are looking for an experienced and customer-obsessed Director of Engineering to lead the development and evolution of our mobile and ... + Establish and uphold technical governance practices to ensure code quality , platform security, and development consistency Customer Experience & Delivery +… more
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