Chemical Laboratory Technician - Quality Control and Development | Chemielaborant (m/w/d) Qualitätskontrolle und Entwicklung

FERCHAU GmbH Niederlassung Frankfurt

Frankfurt am Main, Hessen, Deutschland
Published Mar 20, 2026
Full-time
No information

Job Summary

This role involves a dynamic mix of quality control and developmental support within the pharmaceutical and life sciences sector. As a Chemical Laboratory Technician, you will be responsible for ensuring compliance with DIN EN ISO 13485 and GMP standards for medical devices. Your daily activities will include performing incoming inspections of raw materials and packaging, conducting precise chemical assays using HPLC, titration, and UV-Vis spectrophotometry, and managing batch documentation. Additionally, you will play a key role in equipment qualification, calibration, and laboratory inventory management. This position is particularly attractive due to its permanent contract status with a well-established company offering 60 years of market experience, comprehensive personal coaching throughout the application process, and a robust benefits package including occupational pension schemes and corporate discounts. It offers a structured environment to sharpen your profile in instrumental analytical chemistry within a highly regulated industry.

Required Skills

Education

Completed vocational training as a Chemical Laboratory Technician, Chemical-Technical Assistant (CTA), or a comparable qualification.

Experience

  • Professional experience in instrumental analytical chemistry, specifically with HPLC systems
  • Practical experience in wet chemical analysis methods such as titration and potentiometry
  • Experience working within regulated environments following GMP or ISO 13485 standards
  • Experience in laboratory equipment monitoring, calibration, and documentation
  • Experience with sum parameters (AOX, TOC, COD) is preferred

Languages

German (Fluent)English (Basic)

Additional

  • Must be able to work on-site at the customer location; requires the ability to adhere to strict regulatory documentation standards for medical products.