You will gain in-depth insight into internal and external audit systems and the procedures for authorizing our manufactured products within our Regulatory Affairs/Quality Compliance department, and you will become familiar with internal interfaces such as Production, Quality Control and Engineering
Together with your team, you will be a central point of contact for international authorities and customers on GMP compliance
You will support (international) customer audits and regulatory inspections as well as internal audits — from preparation and participation through to follow-up
You will be involved in the qualification of suppliers and service providers, communicate independently with suppliers and analyze data on your own
You will assist in the creation of risk analyses and in revising SOPs
You will conduct detailed research on regulations and standards for specific topics and present your findings in presentations

You are motivated and studying Biotechnology, Pharmacy, Chemistry, Biology, Pharmaceutical Engineering or a related degree program
You impress us with your friendly, communicative manner and willingness to engage with people; you share a strong commitment to quality and are ready to contribute your ideas
You enrich our team with your initiative, structured and efficient working style, and a goal-oriented approach to new topics
You are available to work with us for six months
You have very good English skills, which you will use in communication with our international suppliers

Attractive compensation
Flexible working hours
Travel allowance
Personal laptop
Self-directed projects run by interns for interns to support networking and career orientation
Thorough onboarding to your new tasks by direct colleagues
Occupational health management, fitness and sports offers
Development opportunities, trust and scope to help shape processes

Internship Quality Compliance, Audit Systems

Key skills