Laboratory Technician as Quality Reviewer in Pharmaceutical Manufacturing | Laborant (m/w/d) als Qualitäts-Reviewer in der pharmazeutischen Fertigung

FERCHAU GmbH Wiesbaden Pharma & Life Science

Wiesbaden, Hessen, Deutschland
Published Feb 20, 2026
Full-time
No information

Job Summary

This role involves ensuring the highest standards of quality within pharmaceutical production by managing and reviewing critical documentation. Day-to-day responsibilities include creating and updating pharmaceutical documents, performing documentation controls, and maintaining technical records such as testing specifications and Standard Operating Procedures (SOPs). You will be responsible for tracking complaints, CAPA measures, and change control requests, as well as releasing batches within the ERP system. The position requires close collaboration with logistics and production planning to prioritize batch releases and optimize operational processes. This is an attractive opportunity for a detail-oriented professional to work with a leading technology service provider, offering a permanent contract and comprehensive coaching throughout the application process. The role is ideal for those who value precision and want to contribute to the safety and efficacy of pharmaceutical products through rigorous quality assurance.

Required Skills

Education

Completed vocational training in a natural science field such as Pharmaceutical Technician, Chemical Technician, Chemical Laboratory Assistant, CTA, PTA, BTA, or a comparable qualification.

Experience

  • Professional experience in pharmaceutical documentation and quality review
  • Practical experience in tracking complaints and CAPA measures
  • Experience in handling technical documents such as testing instructions and SOPs
  • Experience working within an ERP system for batch releases
  • Proven background in a GMP-regulated environment

Languages

German (Fluent)English (Basic)

Additional

  • Must have a strong sense of responsibility and the ability to formulate precise technical documentation. Location constraints or specific travel percentages were not specified.