Manager, Analytical Development

Role: Support analytical development activities for pharmaceutical drug substances and products, focusing on manufacturing at CMOs and maintaining compliance with GMP standards. Responsibilities: review and organize development and manufacturing documents, analyze raw data for batch release and stability, assist with regulatory submission sections, draft SOPs, and provide administrative support. Requirements: BA/BS in a scientific or technical field, 6-8 years in pharmaceutical manufacturing, analytical development, or quality control; proficiency in GMP documentation, MS Office, highly organized and detail-oriented. HighValue: pharmaceutical analytical development, GMP compliance, support for drug substance and product manufacturing, regulatory documentation, working at CMOs. WorkSetup: headquarters-based, US only, full-time employment.