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 May 8, 2026
Full-time
No information

Job Summary

In this role, you will serve as a critical link between laboratory operations and quality assurance within a pharmaceutical manufacturing environment. Your day-to-day responsibilities will focus on the rigorous review, creation, and maintenance of essential pharmaceutical documentation, including Standard Operating Procedures (SOPs) and testing protocols. You will play a key role in ensuring regulatory compliance by managing CAPA measures, handling change control applications, and overseeing complaint tracking. Additionally, you will be responsible for the final release of batches within the ERP system and coordinating with logistics and production planning to prioritize workflows. This position is ideal for a detail-oriented professional with a strong background in natural sciences who thrives on precision and quality management. You will be instrumental in optimizing operational processes while maintaining the high standards required in the pharmaceutical industry, all while supported by a dedicated team focused on your professional development and career placement.

Required Skills

Education

Completed vocational training as a Pharmaceutical Technician, Chemical Technician, Chemical Laboratory Technician, CTA (Chemical-Technical Assistant), PTA (Pharmacy Technician), BTA (Biological-Technical Assistant), or equivalent scientific qualification.

Experience

  • Professional experience in a scientific or laboratory environment
  • Practical experience in pharmaceutical manufacturing or quality control
  • Proven experience with GMP-compliant documentation and regulatory requirements

Languages

German (Fluent)English (Basic)

Additional

  • Not specified