Wetzikon ZH
Quality Manager / Scientifically Responsible Person FvP D/E, 80-100% (m/f/d)
- 28 September 2026
- 80 – 100%
- Permanent position
- German (Fluent), English (Fluent)
About the job
As a successful Regulatory Affairs/Quality/Pharmacovigilance service provider and Clinical Research Organisation, we have been working for research-based pharmaceutical companies at home and abroad for over 45 years. We are looking to strengthen our Quality team immediately or by arrangement.
Quality Manager / Scientifically Responsible Person FvP D/E, 80-100% (m/f/d)
In your new position
- You combine your scientific education and experience in Quality Management in the pharmaceutical environment with a systematic, precise way of working.
- As FvP, you are responsible for product quality and GxP compliance according to Swissmedic requirements, approve batches and handle complaints for partners of Five Office Ltd.
- You create and revise Quality Agreements and process documentation.
- You support the responsible FvP of our sister company Future Health Pharma GmbH.
- If interested, you contribute to further exciting tasks in cooperation with our Life Sciences team, e.g. in Regulatory Affairs or Pharmacovigilance.
- You become part of our Quality team with >10 FvPs and experience the wealth of projects and the broad spectrum of indications of the products supported.
With this background you inspire us
- Pharmaceutical-scientific degree (university degree or equivalent).
- 2–3 years of experience in Quality Management in the pharmaceutical sector as well as sound GMP/GDP knowledge.
- Open, friendly, reliable and competent personality with a high service orientation and a "hands-on" mentality.
- Team player with a structured way of working, personal responsibility and assertiveness.
- Fluent communication in German and English, French is a plus.
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.