Manager, Regulatory & Technical Writing, Process Sciences, Analytics and Technology, Cell and Gene Therapy

Master's degree in Life Sciences, Biotechnology, Engineering, Pharmaceutical Sciences, Regulatory Affairs or related with 8+ years experience, or Bachelor's with 10+ years; significant regulatory/technical writing experience; CMC documentation knowledge; BLA/MAA/NDA submission experience; document management systems like Veeva Vault RIM, QualityDocs, eCTD, SharePoint, Smartsheet.

What you'll do at AstraZeneca:

• leading regulatory writing
• authoring CMC documentation
• coordinating cross-functional reviews

Apply to this Manager, Regulatory & Technical Writing, Process Sciences, Analytics and Technology, Cell and Gene Therapy role at AstraZeneca with a tailored resume on ApplyBolt.