About this job

FERRING GmbH is the German production company of the internationally operating and rapidly expanding FERRING Group, headquartered in Saint-Prex, Switzerland. In Kiel, we produce key products for the pharmaceutical market in the areas of reproductive medicine, endocrinology, urology, pediatrics, and gastroenterology. Using state-of-the-art production facilities, we primarily manufacture sterile dosage forms, specializing in peptide hormones. Research and development are of paramount importance within the FERRING Group and are integral to our company philosophy. Ferring has subsidiaries in nearly 60 countries and markets its products in 110 countries. Our Kiel site employs approximately 550 people.

Changing the lives of millions of people means we succeed together. Our diverse backgrounds, experiences, expertise, and perspectives enable us to find solutions to even the most challenging problems. Imagine the power of your career when it's Ferring + You.

Ferring + You

To support our team in the pharmaceutical department of Ferring Arzneimittel GmbH Marketing- und Vertriebsgesellschaft, we are looking for a motivated and committed student assistant (m/f/d) starting in September 2026.

Look forward to exciting insights into a diverse marketing and sales environment and the opportunity to gain valuable practical experience in an innovative, internationally active pharmaceutical company.

The position involves 7.5 hours per week and is initially limited to one year.

Your contribution to making a difference.

Regulatory Affairs (Drug Approval)

• Support in processing Certificates of Pharmaceutical Product (CPPs)
• Assistance with the revision, maintenance, and updating of registration dossiers

Quality Assurance (Good Distribution Practice, GDP)

• Support in day-to-day operations
• Participation in the creation and maintenance of Standard Operating Procedures (SOPs), the handling of deviations, and other GDP-relevant processes.

Pharmacovigilance

• Support in the collection, documentation and follow-up of adverse event reports
• Maintenance and updating of pharmacovigilance documentation

General support

• Maintenance of databases and document management systems
• Creation of analyses, overviews and reports
• Participation in cross-functional projects

Their qualifications enrich us.

• They are studying pharmacy, life sciences, or a comparable natural science degree program.
• They are interested in the pharmaceutical industry, particularly in the areas of Regulatory Affairs, Quality Assurance and Pharmacovigilance.
• They are characterized by a structured, reliable and independent way of working.
• They have good English skills, both spoken and written.
• Ideally, you should be proficient in using the common MS Office applications.