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Principal Scientist, Early DCT Lead

Merck Sharp & Dohme LLC

NJ

This high-visibility role combines integrated cross-functional program leadership with deep subject-matter expertise (SME) in biologics analytical development. As an Early-Stage DCT Leader,…

Senior Director, Clinical Pharmacology

Keros Therapeutics

Lexington, MA

…(MIDD) strategies across our R&D portfolio. This individual will lead modeling and simulation (M&S) activities from pre-IND through early clinical phases, late-stage global registrational…

Director, Drug Product – Viral Vectors

Insmed Gene Therapy LLC

United States

In this role, you’ll have the opportunity to lead the development, optimization, and scale-up of viral vector drug product processes, including formulation development, fill-finish…

Director, Biologics CMC Technical Writing

RETROPHIN, INC.

SALT LAKE CITY, UT

…patients. Position Summary: The Director, Technical Operations (Biologics CMC Technical Writing) is responsible for the preparation of Chemistry, Manufacturing, and Controls (CMC)…

Director, Biologics CMC Technical Writing

Travere Therapeutics

Denver, CO

• $189,000 to $246,000 USD / year

The Director, Technical Operations (Biologics CMC Technical Writing) is responsible for the preparation of Chemistry, Manufacturing, and Controls (CMC) documentation for regulatory…

Associate Director, Process Development, Cell Therapy

AstraZeneca Pharmaceuticals LP Company

Santa Monica Colorado Avenue, CA

• $138,000 to $207,000 USD / year

…Manufacturing, Quality, Regulatory Affairs, Analytical Development, and CMC teams to ensure robust, compliant, and scalable manufacturing…

Associate Director, Process Development, Cell Therapy

AstraZeneca

Santa Monica, CA · Santa Monica

• $138,000 to $207,000 USD / year

…Manufacturing, Quality, Regulatory Affairs, Analytical Development, and CMC teams to ensure robust, compliant, and scalable manufacturing…

Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME)

Parexel

Phoenix, AZ

Support and lead regulatory compliance activities across global GxP operations, partnering with cross-functional teams to identify, assess, and mitigate compliance risks.

Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME)

Parexel

Springfield, IL

Support and lead regulatory compliance activities across global GxP operations, partnering with cross-functional teams to identify, assess, and mitigate compliance risks.

Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME)

Parexel

Concord, NH

Support and lead regulatory compliance activities across global GxP operations, partnering with cross-functional teams to identify, assess, and mitigate compliance risks.

Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME)

Parexel

Jackson, MS

Support and lead regulatory compliance activities across global GxP operations, partnering with cross-functional teams to identify, assess, and mitigate compliance risks.

Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME)

Parexel

Columbia, SC

Support and lead regulatory compliance activities across global GxP operations, partnering with cross-functional teams to identify, assess, and mitigate compliance risks.

Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME)

Parexel

Honolulu, HI

Support and lead regulatory compliance activities across global GxP operations, partnering with cross-functional teams to identify, assess, and mitigate compliance risks.

Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME)

Parexel

Lincoln, NE

Support and lead regulatory compliance activities across global GxP operations, partnering with cross-functional teams to identify, assess, and mitigate compliance risks.

Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME)

Parexel

Sacramento, CA

Support and lead regulatory compliance activities across global GxP operations, partnering with cross-functional teams to identify, assess, and mitigate compliance risks.

Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME)

Parexel

Helena, MT

Support and lead regulatory compliance activities across global GxP operations, partnering with cross-functional teams to identify, assess, and mitigate compliance risks.

Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME)

Parexel

Bismarck, ND

Support and lead regulatory compliance activities across global GxP operations, partnering with cross-functional teams to identify, assess, and mitigate compliance risks.

Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME)

Parexel

Boston, MA

Support and lead regulatory compliance activities across global GxP operations, partnering with cross-functional teams to identify, assess, and mitigate compliance risks.

Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME)

Parexel

Frankfort, KY

Support and lead regulatory compliance activities across global GxP operations, partnering with cross-functional teams to identify, assess, and mitigate compliance risks.

Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME)

Parexel

Annapolis, MD

Support and lead regulatory compliance activities across global GxP operations, partnering with cross-functional teams to identify, assess, and mitigate compliance risks.

Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME)

Parexel

Denver, CO

Support and lead regulatory compliance activities across global GxP operations, partnering with cross-functional teams to identify, assess, and mitigate compliance risks.

Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME)

Parexel

Des Moines, IA

Support and lead regulatory compliance activities across global GxP operations, partnering with cross-functional teams to identify, assess, and mitigate compliance risks.

Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME)

Parexel

Baton Rouge, LA

Support and lead regulatory compliance activities across global GxP operations, partnering with cross-functional teams to identify, assess, and mitigate compliance risks.

Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME)

Parexel

Carson City, NV

Support and lead regulatory compliance activities across global GxP operations, partnering with cross-functional teams to identify, assess, and mitigate compliance risks.

Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME)

Parexel

Columbus, OH

Support and lead regulatory compliance activities across global GxP operations, partnering with cross-functional teams to identify, assess, and mitigate compliance risks.