- Merck (Rahway, NJ)
- …execution of scientific studies to support development of active pharmaceutical ingredients (APIs), pharmaceutical formulations, and manufacturing processes ... development as well as for the release and shelf-life assessment of clinical materials. + Troubleshoot challenges associated with drug development through active… more
- J&J Family of Companies (Raritan, NJ)
- …Locations:** Raritan, New Jersey, United States of America **Job Description:** Janssen Pharmaceutical , a member of Johnson & Johnson's Family of Companies, is ... will be located in Raritan, NJ! At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working...quality systems. **Preferred:** + Experience with quality support in clinical or GMP manufacturing or support of QC laboratories… more
- Bristol Myers Squibb (Summit, NJ)
- …Codes, and other applicable industry regulations related to the manufacture of pharmaceutical products. Ensure that the right support structure is in place to ... OSHA regulations, and Industry Regulations related to the manufacture of pharmaceutical products. + Develops relationships with diverse groups across the client… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …company - one of Japan's most respected - is a research-driven pharmaceutical company that has tirelessly pursued medical breakthroughs with global reach. Tanabe ... RADICAVA(R) (edaravone) oral suspension in 2022. The company handles research, clinical development, sales, marketing, medical affairs, supply chain, and business… more
- Norstella (Trenton, NJ)
- …dedicated to improving patient access to life-saving therapies. Norstella supports pharmaceutical and biotech companies across the full drug development lifecycle - ... and delivers must-have answers and insights, leveraging AI, for critical strategic, clinical , and commercial decision-making. We help our clients: + Accelerate the… more
- Organon & Co. (Jersey City, NJ)
- …preparation of biowaiver requests for manufacturing site changes or active pharmaceutical ingredient or excipient supply source changes and/or assessment of ... Biopharmaceutics will also be responsible for contributing to and reviewing clinical modules for regulatory submissions, contribute the authoring and review of… more
- Sumitomo Pharma (Jersey City, NJ)
- Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... projects. + Accumulate key competitive information to aid the clinical and marketing teams in drug/brand development. + Identify,...- 3 years of relevant experience in biotech or pharmaceutical industry + 1-3 years of MSL experience in… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial products at CMOs under contract by Otsuka to ensure that ... biologics-specific GMP requirements. This role has global responsibility for directing clinical and commercial product quality to ensure global supply for Otsuka's… more
- Merck (Rahway, NJ)
- …as release and stability testing to support development of active pharmaceutical ingredients (APIs), pharmaceutical formulations, and manufacturing processes ... and implement analytical methods to support release and stability testing of clinical materials. + Perform data entry, data review, and author analytical reports… more
- Taiho Oncology (Princeton, NJ)
- …and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources ... in coordination with internal staff, Japanese colleagues at Taiho Pharmaceutical Corporation (TPC) and external consultants/contractors. Manages the development and… more