GSK seeks a CMC regulatory lead to drive regulatory strategies for investigational, late development and early commercial products. You will coordinate preparation and authorship of technical CMC documents, assess risks, and mentor staff across functions to ensure compliant submissions.
The role requires a Bachelor’s in Life Sciences and 4+ years in global CMC regulatory work, with strong leadership and project management skills.
#J-18808-LjbffrCMC Regulatory Leader — Biopharma Development Projects in upper providence at Unknown Company
This position is listed as full time and onsite.