Internship - Biotech Compliance - All Genders
Internship - Biotech Compliance - All Genders
Internship - Biotech Compliance - All Genders
Internship - Biotech Compliance - All Genders
Merck
Pharmazeutische Produkte, Arzneimittel
Aubonne VD
- Art der Anstellung: Studierende
- Vor Ort
Internship - Biotech Compliance - All Genders
Über diesen Job
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.
Start Date: 01.09.2025
Duration: 6 month
Location: Aubonne, Switzerland
Position: Internship
Role:
The Biotech Compliance Intern will assist in ensuring compliance within the Compliance team at Manufacturing Operational Support by adhering to cGMP standards and ensuring the accuracy of documentation. The intern will contribute to maintaining quality requirements by participating in Deviations, CAPAs, Change Control, and document reviews.
Responsibilities:
- Participate in the resolution of deviations by implementing CAPAs or CCP actions in a timely manner.
- Maintain, review, and manage procedures and/or other documents necessary to uphold the GMP status of activities executed in their area.
- Engage in continuous improvement projects, document changes, and other quality-related activities within the Biotech department.
Skills:
- Understanding of GMP standards and current regulations for the production of active ingredients.
- Awareness of behaviors in a pharmaceutical environment.
- Knowledge of protein manufacturing principles in a pharmaceutical production context.
- Proficiency in office software applications.
Education:
- Currently pursuing a degree in Biotechnology, Life Sciences, Health, or equivalent.
or - Studies related to Compliance or Quality Assurance.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety 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!
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
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