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Chemical laboratory technician (m/f/d)

Langenfeld
GULP – experts united
Inserat online seit: 19 September
Beschreibung

For our client in the field of pharmaceutical analysis, we are looking for an experienced chemical laboratory technician (m/f/d) at the Langenfeld site for analytical method development, validation and performance of analytical tests under GMP conditions.

If you are a team player and interested in multifaceted, challenging tasks, we look forward to receiving your application. Become part of our innovative and dynamic team and shape the future of the company with us.

Randstad Professional welcomes applications from all people. We do not discriminate on the basis of religion, origin, gender, sexual orientation, age, marital status or physical characteristics.

Here's what our clients offer

1. an open corporate culture with flat hierarchies and plenty of creative freedom
2. an international corporate environment
3. Attractive remuneration with profit-sharing
4. Flexible working hours
5. 30 days vacation entitlement plus additional days off
6. Employer-financed company pension scheme
7. Team events

... and much more!

Your tasks

8. Independent performance of pharmaceutical analyses in accordance with laboratory test specifications and test plans
9. GMP-compliant documentation of the tests carried out
10. Preparation of plans and reports (also in English)
11. Release testing of authorized medicinal products
12. Evaluation of analysis data with the aid of chromatography data systems
13. General laboratory activities
14. Independent method development and validation for chromatographic and spectroscopic procedures (HPLC, GC, etc.) on raw materials and finished pharmaceutical products
15. Carrying out skin permeation studies and preparation of biological tissue (e.g. human skin)
16. Optional: equipment and software administration

Your profile

17. Successfully completed training as a chemical laboratory technician / chemical technician, CTA or completed studies (e.g. bachelor's degree in chemistry) or comparable training
18. Ideally 2-3 years of professional experience in a GMP-regulated environment, e.g. in the pharmaceutical industry
19. Good knowledge of HPLC systems
20. Sound experience in the development and validation of analytical methods is an advantage
21. Good MS Office skills, especially Excel
22. Good knowledge of English
23. You are a team player with an independent, structured and careful way of working and good analytical thinking skills

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