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Keywords: Sr. Manager, CMC Regulatory Affairs, Location: USA

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Sr. Manager, Regulatory Affairs CMC

therapies designed to fit seamlessly into daily life. The Sr. Manager, Regulatory Affairs CMC will be an integral part of the... Regulatory Affairs team. This person will be responsible for oversight and execution of drug-device combination product...

Posted Date: 16 Nov 2025

Sr. Manager, CMC Regulatory Affairs

challenge the status quo for the better. Who we are looking for Purpose Currently seeking a Regulatory Affairs (RA) Senior... Manager with strong CMC pre and post approval experience to support Chiesi's Global Rare Diseases (GRD) global portfolio...

Location: USA
Posted Date: 06 Nov 2025
Salary: $121000 per year

Sr. Manager of Regulatory Affairs, Biologicals and Chemicals

Standards, Office Job Description The Sr. Manager, Regulatory Affairs - Drug Support Strategy is a new role responsible... preferred 7 years of experience in CMC regulatory affairs within the pharmaceutical industry 1+ year of prior experience...

Location: New York
Posted Date: 19 Sep 2025
Salary: $118000 - 157000 per year

Senior Regulatory Affairs Specialist

and/or pharmaceuticals including but not limited to healthcare antiseptic products. Under the mentorship of the Sr. RA Manager of Regulatory...Job Description Summary The Senior Regulatory Affairs (RA) Specialist within the BD Interventional Surgical Devices...

Company: BD
Location: Warwick, RI
Posted Date: 13 Nov 2025
Salary: $92700 - 152900 per year

Sr. Manager/Associate Director, Drug Product

-regulatory Affairs, while serving as an important point of technical contact between Eidos and contract manufacturing... drug product disposition. You will also work with colleagues in CMC, Supply Chain Operations, Quality Assurance, and CMC...

Company: BridgeBio
Location: California
Posted Date: 18 Sep 2025
Salary: $160000 - 200000 per year

Sr Oversight Director, Project Management - Respiratory Trials Team - Remote Based in the US

compliant deliverables Advanced, broad understanding of global/regional/national country requirements/regulatory affairs... guidelines; in-depth understanding of a regulatory specialty areas, such as preclinical, clinical, CMC, publishing...

Posted Date: 14 Oct 2025