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Quality Manager / Technically Responsible Person FvP D/E, 80-100% (w/m/d)

Five Office Ltd

Employment type
Full-time
Workload
100%
Location
Wetzikon
Company
Five Office Ltd, 8620 Wetzikon ZH
First posted
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As a successful Regulatory Affairs/Quality/Pharmacovigilance service provider and Clinical Research Organisation, we have been active for over 45 years for researching pharmaceutical companies domestically and abroad. We are looking for reinforcement for our Quality team immediately or by arrangement.

Quality Manager / Technically Responsible Person FvP D/E, 80-100% (w/m/d)

In your new position

  • Combine your scientific education and experience in Quality Management in a pharmaceutical environment with a systematic, exact way of working.
  • As FvP, be responsible for product quality and GxP compliance according to the requirements of Swissmedic, undertake batch releases, and process complaints for partners of Five Office Ltd.
  • Create and revise Quality Agreements and process documentation.
  • Support the responsible FvP of our sister company Future Health Pharma GmbH.
  • If interested, contribute to further exciting tasks in the area of Regulatory Affairs or Pharmacovigilance in cooperation with our Life Sciences team.
  • Become part of our Quality team with >10 FvPs and convince yourself of the abundance of projects and the broad spectrum of indications of the products under supervision.

With this background you will inspire us

  • Pharmaceutical-scientific studies (university degree or comparable).
  • 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 "hands-on" mentality.
  • Team player with a structured way of working, personal responsibility and assertiveness.
  • Business-fluent communication in German and English, French is a plus.

Your FIVE Benefits

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

Have we piqued your interest?

Send your complete application dossier to Andrea Gerber and discover how you can move forward with us.

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