Pharmacovigilance Manager D/E/F, 80-100% (m/f/d)

About the job

We have been active for over 45 years as a successful Regulatory Affairs/Quality/Pharmacovigilance service provider as well as a Clinical Research Organisation for research-based pharmaceutical companies both domestically and abroad. To support our Life Sciences team, we are looking from spring 2027 or by arrangement

Pharmacovigilance Manager D/E/F, 80-100% (m/f/d)

In your new position

• You will contribute your medical-pharmaceutical training or initial experience in local pharmacovigilance for partners of Five Office Ltd and our sister company Future Health Pharma GmbH.
• You will support our experienced Local Safety Officers (LSO) in all activities with the aim of later taking responsibility as an LSO yourself.
• You will deal with tasks related to reports of adverse drug reactions in accordance with the laws and regulations in Switzerland.
• You will be responsible for the target group-appropriate preparation and provision of medical information for various stakeholders.
• If interested, you will contribute in collaboration with our Life Sciences team to other exciting areas of activity, e.g. Regulatory Affairs or Quality Management. Convince yourself of the wealth of projects and the broad indication spectrum of the products supported.

With this background you will inspire us

• Completed studies in medicine or pharmacy and understanding of adverse drug reactions and local pharmacovigilance (CH).
• Team player with a structured and precise way of working as well as personal responsibility.
• Open, friendly and reliable personality with a high level of service orientation and a "hands-on" mentality.
• You appreciate working with authorities, health care professionals, customers and internal teams.
• Negotiation-level communication skills in German, English and French.

Your FIVE Benefits

As a "Best Workplace" we offer a permanent position in a pleasant working environment with partial home office possibility. New horizons through collaboration with our teams in Clinical Research, Regulatory Affairs, Quality Management, Marketing/Communication and Translation. 5 weeks holiday and 3 months sabbatical after 3 years for training or study travel. Contemporary working models and social benefits. Lean structures and short decision-making paths in a dynamic family business. Varied projects with international contacts. Regular events.
Good team spirit.

Have we aroused your interest?

Please send your complete application dossier to Andrea Gerber and discover how you can progress with us.