Laboratory Technician / Chemical Technical Assistant (HPLC/Pharmaceutical Analytics) | Laborant / CTA (m/w/d) HPLC (Pharmaanalytik)

ALS Germany GmbH Altenberge

Münster, Westfalen, Nordrhein-Westfalen, Deutschland
Published Mar 9, 2026
Full-time
No information

Job Summary

As a Laboratory Technician at the Münster location, you will play a critical role in the analysis of mycotoxins and cannabis products within a highly regulated pharmaceutical environment. Your daily responsibilities include performing instrumental analysis using HPLC and GC systems, as well as conducting wet-chemical methods like titrations and detection reactions. You will be responsible for testing pharmaceutical raw materials, active ingredients, and finished products in accordance with international pharmacopoeias such as Ph. Eur. and USP. A significant portion of the role involves working under GMP guidelines, ensuring precise documentation of results in LIMS and Access databases, and assisting with the maintenance and calibration of analytical equipment. This position is particularly attractive for professionals seeking a stable role with 30 vacation days, flexible working hours (Gleitzeit), and comprehensive health and fitness benefits, all while working at the forefront of medicinal cannabis and mycotoxin analytics.

Required Skills

Education

Completed vocational training as a Chemical Laboratory Technician (Chemielaborant), Chemical Technical Assistant (CTA), or Pharmaceutical Technical Assistant (PTA).

Experience

  • 2-3 years of laboratory experience in a GMP-regulated environment is preferred
  • Practical experience in HPLC and GC analytical techniques
  • Professional experience in the chemical and physical testing of pharmaceuticals, active ingredients, and raw materials
  • Initial experience handling narcotics or medicinal cannabis is an advantage

Languages

German (Fluent)English (Basic)

Additional

  • Must be able to work according to German narcotics laws (BtMG and MedCanG). Position is based in Münster/Altenberge. Requires high reliability for GMP-compliant documentation.