- AbbVie (South San Francisco, CA)
- …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Senior Scientist II, CMC Data Strategy is a multidisciplinary expert who ... and data system requirements associated with their Use Cases. The Senior Scientist will partner with Dev Sci colleagues and Information Research as required… more
- Lilly (Indianapolis, IN)
- …medicines to patients who need them all over the world. We are seeking Regulatory Scientist GRA CMC -Parenteral Commercial Products to be a part of the Lilly ... operational support for market registrations and post-approval submissions. The regulatory scientist will leverage CMC technical knowledge and regulatory science… more
- Lilly (Indianapolis, IN)
- …patients who need them all over the world. The Senior Advisor/Director Post approval scientist in Global Regulatory Affairs - CMC commercial solid oral products ... make life better for people around the world. Lilly is looking for post approval regulatory CMC scientists to join us in delivering life-changing new medicines to… more
- Organon & Co. (Plymouth Meeting, PA)
- …Principal Scientist will lead the preparation and submission of CMC dossiers for programs in clinical development, marketing applications and post-approval life ... **Job Description** **The Position** The Associate Principal Scientist (Associate Director) is responsible for developing and implementing Regulatory Chemistry,… more
- Organon & Co. (Jersey City, NJ)
- …for assigned biosimilar projects, with a specific focus on Regulatory CMC (Chemistry, Manufacturing, and Controls) requirements. This role includes oversight of ... development due diligence activities. **Responsibilities** + Provide global strategic regulatory CMC overview for respective products and portfolio. + Serve as the… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Join Gilead and help create possible, together. **Job Description** The Scientist , Cell Culture Process Development (Pre-Pivotal) will lead and execute cell ... culture process development for Gilead biologics entities during pre-pivotal phases development (pre-clinical, phase I/II), including experimental design, laboratory execution, and process transfer. He/she will also lead and execute laboratory experimentation… more
- Atlantic Health System (Pompton Plains, NJ)
- …+ High school diploma or equivalent required + Documented training as defined in the CLIA regulation 42CFR493.1489(b) + Non-degree semester hours in medical ... Responsible for a variety of routine and complex technical tasks in the performance of laboratory tests to obtain data for use in the diagnosis and treatment of disease. Principal Accountabilities: + Comfortable with emergency situations such as Massive… more
- Lilly (Indianapolis, IN)
- …medicines to patients who need them all over the world. The Advisor Post approval scientist in Global Regulatory Affairs - CMC Commercial Products will leverage ... medicines that make life better for people around the world. Lilly is looking for post approval regulatory CMC scientists to join us in delivering life-changing new… more
- Lilly (Indianapolis, IN)
- …make life better for people around the world. Lilly is looking for regulatory CMC scientists to join us in developing and bringing life-changing new medicines to ... all over the world. The Senior Advisor/Director in Global Regulatory Affairs - CMC Pre-approval Small Molecules will leverage CMC technical knowledge and… more
- Sanofi Group (Cambridge, MA)
- **Job Title** : Analytical Principal Scientist (Analytical team lead) **Location:** Cambridge, MA **About the Job** Are you ready to shape the future of medicine? ... individual to join our analytical group as a principal scientist . The group is part of the synthetic platform...group is part of the synthetic platform within Global CMC Development with focus on small molecules that is… more