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

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 1. The manager will be responsible for creating requirement documents for investment projects, assisting in the selection of investment objects through decision analysis, and ensuring timely and GMP-compliant project implementation. Key duties also include comprehensive project documentation, regular status reporting, and transparent communication of results and challenges. The position supports digitalization initiatives, maintains and develops concepts for workflow optimization, and defines measures within the Change Control process. Additionally, the role contributes to qualification projects, initiates corrective and preventive actions (CAPA), change controls, risk analyses, and root-cause analyses, and manages material flow control. This is an attractive opportunity for a detail-oriented professional with a background in pharmaceutical manufacturing and strong GMP knowledge to contribute to a future-oriented and family-like company culture.

Required Skills

Education

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

Experience

  • Professional experience in pharmaceutical manufacturing
  • Experience with pharmaceutical process technologies
  • Experience with regulatory EU-GMP knowledge

Languages

German (Fluent)English (Fluent)

Additional

  • Not specified