Intern Compliance

vor 1 Monat


Aubonne, Schweiz Merck KGaA Darmstadt Germany Vollzeit

Work Your Magic with us

Ready to explore, break barriers, and discover more? We know you've got big plans - so do we Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

**Your role**:
We offer a 6 to 12 months internship within the packaging department of our site in Aubonne, Switzerland.

Your focus will be on compliance, and you will be working with us to redefine and reorganize our full set of GMP documentation and training.

Our compliance experts have in collaboration with quality assurance identified a huge opportunity to increase compliance and efficiency in parallel. To reach this target we must redesign and restructure our base of standard operating procedures (SOPs). Procedures must be re-aligned and mutually optimized, requiring many procedures to be completely re-written.

Our documentation and training base is very substantial, participating in this project will give you an insight and knowledge of all the required processes and tasks to be defined and regulated within a fully GMP compliant packaging operation. At the same time, you will understand the importance of optimization and efficiency, which must go hand in hand with GMP to guarantee patient safety and optimize business potential.

**Your profile**:

- A relevant diploma in Life-science (Master - ongoing)
- Knowledge in Biotechnological sciences is a plus
- Fluently spoken and written English and French
- Good editorial and communication skills
- Ability to synthesize effectively
- Autonomous

**What we offer**:We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress


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