We are currently looking for a Senior Process Advisor (m/f/d) on behalf of our business partner from the pharmaceutical industry in Biberach .
Here's what we offer
1. Attractive salary and long-term job security through group affiliation
2. Up to 30 days vacation per year
3. Contribution to company pension scheme after end of probationary period
4. Extensive social benefits, including Christmas and vacation bonuses
5. Reimbursement of travel expenses
6. Generally an open-ended employment contract
7. Good chances of being taken on by our business partners
8. Tailored further training opportunities and free language courses
9. A wide range of employee benefits
Your tasks
10. In your new role, you will be responsible for coordinating work packages, optimizing processes and further developing the GMP status within the Cell Culture division.
11. You will design well thought-out solutions and ensure their successful implementation.
12. You will be responsible for production support/coordination and technical management as well as the definition of specifications for the process, taking into account the required cGMP-compliant operation, quality-relevant aspects and occupational safety aspects.
13. In addition, you will be involved in the evaluation of process data (creation of charts, tables, interpretation), process monitoring and troubleshooting activities.
14. You will also be responsible for the independent planning, implementation and evaluation of expert activities for technical projects and take on special tasks such as the independent implementation of error analyses, preparation of regulations and risk analyses.
15. You will support the Cell Culture department in the implementation of new technologies and processes, including as part of a project.
Your profile
16. Completed studies (Bachelor's, Diploma, Master's) in biopharmacy, biotechnology, bioengineering or a completed scientific education with additional training as a master craftsman or technician as well as several years of professional experience - ideally in dealing with large-scale production facilities under GMP conditions
17. Expertise in working with systems such as GBS, LIMS, SAP and BioMES as well as experience in a GMP-regulated environment
18. In-depth MS Office applications and a good understanding of complex interrelationships
19. Independent problem identification and solution with a structured way of working
20. Proactive and independent way of working with a high level of initiative and ability to communicate complex content
21. Good knowledge of English