Planet Pharma is seeking an Associate Director, Analytical Development to lead late-stage analytical strategy for a lipid-peptide inhalation product. You will oversee regulatory authoring, method development, and stability programs, working with CDMOs and internal teams to ensure robust data packages for BLA submissions.
Responsibilities include managing analytical development projects, directing method transfer/validation, and ensuring cGMP-compliant processes.
#J-18808-LjbffrDirector of Analytical Development & Regulatory Submissions in california at Unknown Company
This position is listed as full time and onsite.