Quality Officer | Quality Officer | M/W/D - Referenz 001007

consult16 GmbH

Biberach an der Riß, Baden-Württemberg, Deutschland
Published Aug 11, 2025
Full-time
Fixed-term

Job Summary

As a Quality Officer for an internationally successful pharmaceutical company in Upper Swabia, you will play a crucial role in ensuring regulatory compliance and adherence to international cGMP and internal regulations within the BioPharma Drug Product unit. Your daily tasks will involve reviewing and approving change requests and documents, supporting the improvement of the internal quality management system, and defining consistent standards. You will serve as the primary contact for quality-related inquiries in the Change Control Process across various areas, including sterile manufacturing, packaging, and quality control of biopharmaceuticals. This role requires proactive decision-making on routine tasks, diligent tracking of quality-relevant assignments, and escalation when necessary. The ideal candidate will possess a degree in Pharmacy, Biopharmacy, Biology, or Chemistry, coupled with extensive professional experience in biopharmaceutical manufacturing and a strong understanding of GMP compliance and regulatory requirements. This is an attractive opportunity for a professional seeking to contribute to high-standard quality assurance in a dynamic pharmaceutical environment.

Required Skills

Education

Bachelor's or Master's degree in Pharmacy, Biopharmacy, Biology, or Chemistry, or comparable qualification

Experience

  • Several years of professional experience in Pharmacy, Biopharmacy, Biology, or Chemistry
  • Several years of experience with GMP Compliance and quality topics
  • Advanced knowledge of biopharmaceutical manufacturing, especially regarding compliance and quality-relevant topics in process and quality control

Languages

German (Fluent)English (Basic)

Additional

  • Temporary contract for 18 months; Must be able to start as soon as possible; Position is based in Upper Swabia, Germany.