Associate Director, CMC Regulatory Affairs (Cell & Gene Therapies)
AZ is hiring for Associate Director, CMC Regulatory Affairs (Cell & Gene Therapies) in US - Cambridge Kendall SQ - MA. Hybrid, Executive level, $136k–$203k a year stated. First seen November 10, 2026; open as of November 13, 2026. Jobs taken straight from company career pages — no aggregator in between.
With Destava: How well do you fit? · Tailor my résumé · Write a cover letter
- Company
- AZ
- Where
- US - Cambridge Kendall SQ - MA
- Arrangement
- Hybrid
- Level
- Executive
- Pay stated
- $136k–$203k a year
- First seen
- November 10, 2026
- Listed via
- Workday
What the posting says
This position is hybrid, and may be based in Santa Monica, CA, Gaithersburg, MD or Boston, MA and reports to the Senior Director, CMC-CGT Regulatory Affairs. Essential Functions and Responsibilities - Interpret global regulations and guidance to identify risks and provide input for guidance to cross functional product teams. - Partner with cross-functional stakeholders to deliver regulatory dossiers (e.g. CMC component(s) of IND / IMPD / BLA/ Master Files, amendments, annual reports) and health authority interaction briefing documents. Manage regulatory dossiers throughout the product…
Read more and apply on AZ's site
More jobs like this
A search agent finds the jobs this list misses: the ones that mean the same without the same words. Have Destava watch for associate director, cmc regulatory affairs (cell & gene therapies) jobs in US - Cambridge Kendall SQ - MA, new matches every morning on your own account.
This page includes information from the O*NET 31.0 Database by the U.S. Department of Labor, Employment and Training Administration (USDOL/ETA). Used under the CC BY 4.0 license. O*NET® is a trademark of USDOL/ETA.