QC Lab Team Supervisor – Pharmaceutical Quality Control | QC Lab Team Supervisor (m/w/d) – Pharmazeutische Qualitätskontrolle

BS Wutow GmbH

Frankfurt am Main, Hessen, Deutschland
Published Nov 11, 2025
Full-time
Permanent

Job Summary

This is a critical full-time position starting December 1, 2025, within a leading pharmaceutical company in the Rhein-Main region, offering a direct path to permanent employment. The QC Lab Team Supervisor is responsible for ensuring the timely execution and GMP-compliant documentation of all quality testing for pharmaceutical products. Key daily activities include implementing and managing essential quality assurance systems such as OOS/OOT, Change Controls, and Deviation management, while upholding strict data integrity guidelines. The role involves providing expert support during regulatory authority inspections and internal quality audits, coordinating validation and transfer studies, and handling annual product reviews and customer complaints. Candidates must possess a natural science degree (e.g., Chemistry, Biology, or Pharmacy), fundamental GMP knowledge, and either initial experience in personnel leadership or a strong motivation to assume supervisory responsibilities. This role offers significant responsibility and the opportunity to shape quality processes in a modern, high-standard GMP laboratory environment.

Required Skills

Education

Successful completion of a natural science degree (Bachelor, Diploma, or Master) in fields such as Chemistry, Biology, Pharmacy, or related disciplines.

Experience

  • Fundamental knowledge of GMP (Good Manufacturing Practice)
  • Initial professional experience in pharmaceutical Quality Control (ideal)
  • Initial personnel experience or strong motivation to assume leadership responsibility

Languages

English (Intermediate)

Additional

  • Start date of December 1, 2025. Must be able to work full-time (37.5 hours/week) in the Rhein-Main Area, Germany.