Employee Quality Control Laboratory

Employee Quality Control Laboratory (m/f/d)

Helaxa is a company in Luckenwalde founded in 2022 by Erol Isim and the traditional family business HELM AG and specialises in the production of the life‑saving active ingredient heparin. On a total area of 22,500 square metres, the most modern and efficient production facility in Europe is being built, which will meet the highest quality standards.

Date: Nov 6, 2025
Location: Luckenwalde, DE, 14943
Business Unit: Helaxa GmbH & Co KG
Job Function: Quality Management / HSE
Level of Experience: Mid‑Career

"Caring today. Enabling tomorrow" is more than just a slogan for us. It is the daily inspiration for collaboration, as well as all our actions and decisions. This describes the philosophy of Helaxa, a newly established company in Luckenwalde dedicated to manufacturing active ingredients for life‑saving medicine. For our dynamic and growing company in Luckenwalde, we are seeking dedicated talents (m/f/d) who are motivated to drive our mission ‘Caring today. Enabling tomorrow' with passion.

Position Objective

Facilitate timely execution of QC tests on incoming samples of raw materials, intermediate, and finished products according to established testing procedures, as well as participating in maintaining the qualification/validation status of equipment and methods within the quality control laboratory.

Key Responsibilities

• Independently process incoming sample materials including sampling in accordance with current test instructions
• Perform and document method implementation/validation studies and take ownership for maintenance and condition of instruments
• Contribute to the internal quality management system (training, self‑inspections, etc.)
• Participate in overarching, cross‑functional projects, as needed
• Communicate with other departments to ensure smooth operations

Your Profile

• Training on the job as a chemical laboratory technician or equivalent qualification
• Working experience in pharmaceutical quality control of active ingredients, ideally with experience in the field of rt‑PCR
• Strong analytical and technical understanding
• Good working knowledge in evaluation and documentation of laboratory tests/results in a GMP environment
• Proficient in office standard software and laboratory equipment/LIMS applications
• Structured, solution‑oriented, self‑motivated work approach, with a hands‑on mentality
• Ability to work independently in a small team, pro‑active attitude and strong quality mindset
• Excellent German language skills, both written and spoken, willingness to work early/late shifts

Does this sound like you?

Then we look forward to receiving your detailed application via our application portal.

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