Pharmaceutical Production Specialist / QA Reviewer | Pharmakant (m/w/d)

Randstad Professional

Frankfurt am Main, Hessen, Deutschland
Published Aug 12, 2025
Full-time
Permanent

Job Summary

This role involves ensuring the quality and compliance of pharmaceutical production documentation. The successful candidate will primarily review manufacturing documentation within the ICF Quality Unit Devices Packaging, prioritize work for batch release, and verify documentation for pharmaceutical-technical complaints. They will also be responsible for initiating actions for discrepancies, archiving batch records, and supporting the onboarding of new employees. This position is ideal for a detail-oriented professional with a background in pharmaceutical or chemical production, looking to contribute to quality assurance and process optimization in a highly regulated industry. The role offers the chance to work closely with QA Managers and Qualified Persons, ensuring GMP compliance and timely training completion.

Required Skills

Education

Completed training as a Pharmaceutical Production Specialist or Chemical Production Specialist

Experience

  • Professional experience in the pharmaceutical industry or a similarly regulated field
  • Experience in quality within the industrial sector (pharmaceutical or food) is advantageous
  • GMP experience is desirable
  • Experience with SAP Calypso is ideal
  • Practical experience in documentation is advantageous

Languages

German (Fluent)

Additional

  • Not specified