Quality Assurance Associate | Mitarbeiter Qualitätssicherung (m/w/d)

Orizon GmbH Niederlassung Bad Homburg

Friedrichsdorf, Taunus, Hessen, Deutschland
Published Mar 6, 2026
Full-time
Permanent

Job Summary

This role involves supporting an established pharmaceutical company in ensuring high quality standards for products and processes. As a Quality Assurance Associate, you will be responsible for performing GMP-compliant documentation of analyses, including release testing and stability studies. You will utilize various analytical methods such as HPLC, GC, IR, and UV spectroscopy in accordance with international pharmacopoeias like Ph. Eur. and USP. The position requires recording and verifying analytical results while creating necessary documentation within your scope of responsibility. This is an attractive opportunity for a professional with a background in chemical laboratory work to join a leading industry player. The role offers a competitive salary under the GVP collective agreement, up to 30 days of annual leave, and the potential for permanent takeover by the client company. It is ideal for detail-oriented individuals who value integrity and quality in a regulated environment.

Required Skills

Education

Completed vocational training as a Chemical Laboratory Assistant (Chemielaborant) or a comparable qualification.

Experience

  • Professional experience as a Chemical Laboratory Assistant or in a comparable analytical role
  • Experience in performing and documenting analyses according to GMP standards
  • Practical experience with analytical methods including HPLC, GC, IR, and UV
  • Experience working with international pharmacopoeias and regulatory requirements

Languages

German (Fluent)

Additional

  • The position is a full-time, permanent contract. Applicants should provide their availability and salary expectations. Location-based work in a pharmaceutical laboratory environment is required.