Time for change - time for a new job! Are you a scientist looking for a new professional challenge in the field of ITOT Compliance in Penzberg ? Randstad Professional has what you are looking for: A secure job, attractive benefits and a job with exciting tasks in the pharmaceutical sector .
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
● Creation, processing, follow-up and closure of changes, deviations, corrections and preventive measures
● Performing quality assurance tasks for the unit's QA, IT and automation systems, including associated processes (e.g. archiving, maintenance of master data and maintenance contracts, data integrity)
● Creation and processing of risk analyses in the quality risk management environment
● Ensuring operational GMP-relevant documentation (e.g. records management) or the creation and processing of regulations (e.g. content management) in the automation environment
● Preparation, support and follow-up of audits and inspections
● Representation of the unit with regard to QA and training topics, as well as the implementation and organization of training courses in the unit
● Supporting validation and qualification projects and participating in the establishment of new IT & automation systems
Your profile
10. Bachelor, Master, Diploma, e.g. chemical engineer, biotechnology engineer, university degree in the field of computer science, chemistry, biology, biotechnology, process engineering or an equivalent technical education with experience from practical activities
11. 4-6 years of professional experience after graduation (no graduates without non-university professional experience, internships or similar during the course of studies do not count)
12. Experience in quality assurance
13. Experience in the GMP environment is an advantage
14. Experience as a (partial) project manager or in-depth knowledge of automation technology or complex IT systems
15. Knowledge of pharmaceutical manufacturing and software development processes
16. Specialized knowledge and limited management tasks or responsibility for sub-areas, ongoing activities, targets and product portfolios
17. Meticulous way of working
18. Fluent German and good English skills