If you are thinking about a new career start, then we should talk! We currently have an exciting position as Specialist Team Process Control (m/f/d) with a business partner in the Rhine/Main areaarea. Diverse tasks, a working atmosphere characterized by appreciation and attractive benefits are waiting for you - all in an temporary employment with a customer from the pharmaceutical industry. Sounds good? We look forward to receiving your online application. Equal opportunities are very important to us - applicants with a disability are very welcome
Here's what we offer
1. Attractive salary and long-term job security through group affiliation
2. Contribution to company pension scheme after end of probationary period
3. Extensive social benefits, including Christmas and vacation bonuses
4. Reimbursement of travel expenses
5. Generally an open-ended employment contract
6. Good chances of being taken on by our business partners
7. Tailored further training opportunities and free language courses
8. A wide range of employee benefits
Your tasks
9. Review of the manufacturing documentation for CSI's production facilities (GMP documents, plant logbooks, EBR, MBR, MCR, additional documentation, signature control lists)
10. Checking all GMP and compliance-relevant aspects in the documents
11. Identification of deviations and anomalies in the executed manufacturing documentation as well as sources of error and optimization potential in the master documentation
12. Coordinating all activities with production operations, quality assurance and other functions involved
13. Supporting companies with questions and error analyses relating to the GMP-compliant completion of manufacturing and cleaning documents
Your profile
14. Completed vocational training in a chemical/pharmaceutical field, e.g. chemical technician, pharmaceutical technician, chemical laboratory technician or comparable qualification
15. First professional experience in a comparable position
16. Background knowledge of production processes in chemical production / GMP production
17. Independent and solution-oriented way of working