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Regulatory Affairs CMC Lead Gene Therapy

AskBio Asklepios BioPharmaceutical, Inc.
United States only

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A leading gene therapy company is seeking an Associate Director for Regulatory Affairs, CMC. This role will manage CMC strategy and coordinate regulatory activities to ensure timely registration of gene therapy products. Candidates should have over 8 years of CMC drug development experience and extensive knowledge of regulatory submissions for gene therapy. The position offers the chance to drive innovative regulatory strategies and ensure compliance with industry standards onsite or in a remote work setting.
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About the job

Apply before

Posted on

Job type

Full Time

Experience level

Senior

Location requirements

United States

Hiring timezones

United States +/- 0 hours

Job categories

Compliance & Regulatory AffairsRegulatory Affairs LeadRegulatory Affairs DirectorRegulatory Affairs CMCCMC Regulatory Affairs DirectorDirector Regulatory Affairs

Skills

Regulatory AffairsCMCGene TherapyRegulatory SubmissionsDrug DevelopmentRegulatory Strategy Remote

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