Project and GMP Compliance Manager for Production Area II | Projekt- und GMP-Compliance-Manager (m/w/i) für den Produktionsbereich II

MEDICE Arzneimittel Pütter GmbH & Co. KG

Iserlohn, Nordrhein-Westfalen, Deutschland
Published Aug 21, 2025
Full-time
No information

Job Summary

This role involves leading technology, process, and GMP compliance projects within Production Area II, focusing on pharmaceutical manufacturing. The manager will be responsible for creating requirement documents for investment projects, assisting in the selection of investment objects, and ensuring projects are completed on schedule and in compliance with GMP regulations. Key responsibilities include comprehensive project documentation, regular status reporting, and transparent communication of results. The position also supports digitalization initiatives, optimizes workflows, and manages change control procedures. Additionally, the role involves planning and executing packaging validation, contributing to qualification projects, and implementing corrective and preventive actions (CAPA). This is an excellent opportunity for a professional with a background in pharmacy or a related scientific field to contribute to a future-oriented, family-like company committed to long-term growth and innovation in pharmaceutical production.

Required Skills

Education

Completed training as a Pharmaceutical Master (Pharmameister) or a degree in Pharmacy, Pharmaceutical Technology, or an alternative technical/natural science background.

Experience

  • Professional experience in pharmaceutical manufacturing (ideally)
  • Experience with pharmaceutical process techniques (beneficial)
  • Experience with regulatory EU-GMP knowledge (beneficial)

Languages

German (Fluent)English (Fluent)

Additional

  • Not specified