PTA (m/w/d) - Mitarbeiter für wissenschaftliche Produktdokumentation und regulatorische Produktdaten

Maintain and update product files, specifications, and raw material documents to ensure they remain complete, current, and consistent across all systems. Create and verify LMIV files alongside scientific and regulatory product master data while performing version control and consistency checks between formulations, labels, and records. Request missing or incomplete supplier documentation and prepare standardized regulatory procedures, including BVL, IFA, and PZN notifications, as well as export materials. Work closely with scientists, biochemists, and regulatory affairs teams within ZEINpharma's family-owned structure in Nauheim, supporting the development and manufacturing of over 170 premium micronutrient products for global customers.