Laboratory Technician and 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 Apr 13, 2026
Full-time
No information

Job Summary

This role involves ensuring the highest standards of quality within a pharmaceutical manufacturing environment. As a Quality Reviewer, you will be responsible for the creation, review, and updating of critical pharmaceutical documentation, including Standard Operating Procedures (SOPs) and testing specifications. Your daily activities will include performing documentation controls, tracking complaints, managing CAPA (Corrective and Preventive Actions) measures, and handling Change Control requests. You will also play a key role in the logistics chain by releasing batches in the ERP system and coordinating with the logistics and production planning departments to prioritize releases. This position is ideal for a detail-oriented professional who enjoys process optimization and cross-departmental collaboration. Joining FERCHAU offers the unique advantage of professional coaching throughout the application process, a permanent employment contract, and exposure to prestigious clients within the pharmaceutical industry.

Required Skills

Education

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

Experience

  • Professional experience in pharmaceutical manufacturing or laboratory environments
  • Demonstrated experience in creating and reviewing pharmaceutical documentation and technical records
  • Proven track record of working within strict GMP-regulated environments
  • Experience handling quality management processes such as CAPA, Change Control, and complaint tracking
  • Experience using ERP systems for batch release and inventory management

Languages

German (Fluent)English (Basic)

Additional

  • Must have the ability to formulate precise and concrete technical documentation; high level of responsibility and quality-oriented mindset required.