We create lasting connections: Thanks to our trusting contacts with local HR decision-makers, we can offer you attractive jobs with successful companies in the pharmaceutical sector. We are currently looking for an experienced Process Engineer in Singen. Are you a biotechnologist looking for a secure job with fair pay and long-term prospects? You'll find what you're 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. Performance-oriented salary package depending on qualifications and professional experience
2. Attractive social benefits, for example vacation and Christmas bonuses
3. Vacation entitlement of up to 30 days per year
4. Good chances of being taken on by our client company
5. Individual training with renowned partners
6. A wide range of employee benefits
7. Possibility of predominantly working from home by arrangement
Your tasks
8. Perform change control, investigations, CAPAs and continuous process improvements during validation/manufacturing activities
9. Manage work packages for capital projects in compliance with timelines, policies and procedures
10. Support qualification of new vaccine manufacturing facilities and equipment in compliance with cGMP requirements and global regulatory requirements
11. Assist in the planning, execution and reporting of validation activities, including analyzing data and determining results and conclusions
12. Collaborate with QA, Quality Control and other support functions to ensure the smooth flow of technology transfer and validation
13. Responsibility for recipes and recipe lists
14. Coordination of technology transfer as representative of the Receiving Unit
15. Troubleshooting and improvements during technology transfer
16. Responsibility for the creation and content of bills of materials (BOM) for raw materials and single-use materials
17. Support in setting up the practical process in production
Your profile
18. University degree in biotechnology or a related field
19. Several years of experience in supporting start-ups, technology transfer and maintaining cGMP-compliant biopharmaceutical manufacturing processes
20. Sound knowledge of GMP
21. Ideally experience in working with live viruses
22. Experience in writing technical documents, including validation documents, protocols and reports
23. Experience in the use of statistical analysis tools and Design of Experiments (DoE) an advantage
24. Technical knowledge within biological drug manufacturing
25. Very good written and spoken German and English skills
26. Enjoy interdisciplinary and cross-functional teamwork
27. Organizational talent and a goal-oriented way of working