Showing 1-10 of 93
Showing 1-10 of 93
Cmc regulatory specialist jobs

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Sun Pharmaceutical Industries, Inc. - Cranbury, NJ

Prepare CMC documents for regulatory submission. AR&D Document Specialist/AR&D Documentation Specialist. Must have an appropriate understanding of ICH and FDA...

Regeneron - Rensselaer, NY

Coordinates the timely and accurate assembly of responses to inquiries from Regulatory agencies on CMC content of regulatory submissions....

Regeneron - Rensselaer, NY

Works with regulatory contacts on the preparation of CMC sections of new drug submissions, amendments and other regulatory documents for US, Canada, and other...

Regeneron - Rensselaer, NY

Title level (Associate Specialist, Specialist, or Senior Specialist) will be determined based on skills and experience....

Regeneron - Rensselaer, NY

Coordinates and/or oversees the timely and accurate assembly of responses to inquiries from regulatory agencies on CMC content of regulatory submissions....

Shire Pharmaceuticals - Lexington, MA

Support authoring and review of CMC sections of filings related to external validation activities and response to questions from agencies as needed....

BioPoint - Lexington, MA

BioPoint is seeking to hire a Regulatory Affairs CMC (Chemistry, Manufacturing, Controls) Specialist for a position in Lexington, MA....

Boehringer Ingelheim - Ridgefield, CT

Responsibilities also include collaboration with regulatory information manager, Product and CMC managers, other regulatory and contributing disciplines, e.g....

AbbVie - Lake County, IL

We are scientists, researchers, communicators, manufacturing specialists, and regulatory experts. CMC Development Strategy:....

Allergan - Jersey City, NJ

Interact with Medical, Regulatory, CMC, Biostatistics, Project Management, Finance, PK and QA groups on a regular basis to meet the needs of the clinical...


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