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
Job Summary
This role involves ensuring the highest standards of quality within a pharmaceutical production environment by managing and reviewing critical documentation. Day-to-day, you will be responsible for creating, auditing, and updating technical documents, including test specifications and Standard Operating Procedures (SOPs). You will play a pivotal role in the batch release process within the ERP system, coordinating with logistics and production planning to prioritize releases. Additionally, you will track complaints, CAPA measures, and change control requests while participating in process optimization. This position is ideal for detail-oriented professionals with a background in laboratory science who enjoy the intersection of technical documentation and regulatory compliance. The role offers the stability of a permanent contract and the opportunity to work with high-profile clients in the pharmaceutical industry through FERCHAU’s extensive network, providing a structured path for career development in quality management.
Required Skills
Education
Completed vocational training as a Pharmaceutical Technician, Chemical Technician, Laboratory Assistant (CTA, PTA, BTA), or a comparable scientific qualification.
Experience
- Professional experience in pharmaceutical or chemical laboratory environments
- Demonstrated experience in creating and reviewing pharmaceutical documentation and technical instructions
- Practical experience with GMP requirements and quality control standards
- Experience in handling complaints, CAPA, and change control processes
- Experience using ERP systems for batch release and logistics coordination
Languages
Additional
- Must have a high sense of responsibility and the ability to formulate technical information precisely. Position requires location-based work at the client site.
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