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Team leader quality assurance (m/f/d)

Frankfurt am Main
GULP – experts united
Teamleiter
Inserat online seit: 25 November
Beschreibung

We create lasting connections: Thanks to our trustworthy contacts with local HR decision-makers, we can offer you attractive jobs with successful companies in the pharmaceutical industry in Frankfurt am Main. We are currently looking for a Supervisor in Quality Control. Are you a pharmacist or biotechnologist looking for a secure job with fair pay and long-term prospects as a QC Lab Team Supervisor? You will find what you are looking for with us - apply now! Our working atmosphere and the openness of our teams promote equal opportunities for all people - including those with disabilities, whose applications we welcome.

Here's what we offer

1. Above-average salary
2. Attractive social benefits, for example vacation and Christmas bonuses
3. Vacation entitlement of up to 30 days per year
4. Opportunity to be taken on by our business partner
5. Regular team events such as summer parties and Christmas parties
6. Monthly changing employee offers, e.g. for technology, fashion, cars, etc.

Your tasks

7. Ensuring the timely execution and documentation of quality inspections of pharmaceutical products in compliance with GMP guidelines and other requirements
8. Implementation and support of required quality assurance systems, e.g. failure investigation, under the responsibility of the responsible quality management and head of quality control
9. Implementation of the inspection-compliant quality concept by contributing expert knowledge during inspections by the authorities and internal quality audits
10. Implementing regulations on occupational safety and health and environmental protection (HSE) and monitoring compliance with these rules
11. Maintaining and approving sampling plans, test methods and test specifications as well as the associated acceptance criteria
12. Planning, coordination and evaluation of verification, validation and transfer studies in compliance with relevant internal and external guidelines
13. Implementing data integrity specifications and ensuring compliance
14. Preparation of the annual product evaluation
15. Processing complaints in relation to laboratory tests
16. Collaboration in project teams

Your profile

17. Successfully completed scientific studies
18. Professional experience desirable
19. Ideally initial experience in managing employees
20. Knowledge of GMP and expertise in QC
21. Experienced with MS Office
22. Good written and spoken English skills
23. Independent, proactive and conscientious way of working as well as quick comprehension skills
24. Willingness to perform and a strong sense of responsibility

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