- Takeda Pharmaceuticals (Boston, MA)
- …the best of my knowledge. **Job Description** **About the role:** Join as a Digital CMC Scientist to support the planning, development and execution of the In ... R&D context. In this role, you will work closely with the Sustainable CMC and Innovation team as well as capability leads from all development functional… more
- Sanofi Group (Waltham, MA)
- **Job Title:** Senior Associate Scientist , GMU CMC Drug Product Development **Location** : Waltham, MA **About the Job** Are you ready to shape the future of ... progress. Join our Genomic Medicine Drug Product Development Team as a Senior Associate Scientist and you'll have the opportunity to work on different facets of drug… 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
- Merck (Madison, WI)
- **Job Description** **Director, Combination Product Regulatory CMC - (R5)** This Principal Scientist position is equivalent to a Director position. Under ... direction from the Combination Product Regulatory CMC Team Leader, the Principal Scientist is responsible for executing in the Regulatory CMC space.… more
- Cardinal Health (Dover, DE)
- …Cardinal Health's Regulatory Science clients. Working remotely under the supervision of the CMC Supervisor, the Scientist I builds and formats Common Technical ... to Cardinal Health_** The _Scientist I, Chemistry, Manufacturing, and Control ( CMC )_ ensures efficient and quality production of product submission dossiers for… more
- Lilly (Carolina, PR)
- …all over the world. The Sr. Principal Scientist **or** Advisor Post Approval Scientist in Global Regulatory Affairs - CMC Commercial Products will leverage ... people around the world. Lilly is looking for post approval regulatory CMC (Chemistry, manufacturing and controls) scientists to join us in delivering life-changing… 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
- LGC Group (Petaluma, CA)
- …Working Hours: Tuesday-Friday (4 x 10 hours, 6am - 4:30pm). The QC Associate Scientist brings scientific experience to LGC and is open to both learning more and ... sharing knowledge with others. You will be part of an ambitious and collaborative team that strives for flawless execution in all tasks. + Setting up instrument sequences, while monitoring analysis and data + Performing instrument troubleshooting, maintenance,… 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
- Astellas Pharma (South San Francisco, CA)
- ** Scientist II, Bioassay & Research** Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven ... For more information, please visit our website: www.astellasgenetherapies.com. **The Role:** The Scientist II will take a lead in developing and transferring assays… more
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