Quality Manager / Technically Responsible Person FvP D/E, 80-100%
- Employment type
- Full-time
- Location
- Wetzikon · Remote possible
- Company
- Five Office Ltd, Guyer-Zeller-Strasse 10, 8620 Wetzikon ZH
- First posted
Quality Manager / Technically Responsible Person FvP D/E, 80-100% (m/f/d)
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 at home and abroad. We are looking for reinforcement for our Quality team immediately or by arrangement.
Your new position combines your scientific education or experience in Quality Management with a systematic and exact way of working. For partners of Five Office Ltd, you take responsibility for product quality and GxP compliance, perform batch releases, process complaints, etc. Additionally, you create and revise Quality Agreements and process documentation.
For our sister company Future Health Pharma GmbH, you support the responsible FvP in their tasks.
In cooperation with our Life Sciences team, exciting tasks in the areas of Regulatory Affairs, clinical trials or pharmacovigilance offer individual development opportunities if interested. They attest to the abundance of our projects and the supervised products.
With this background, you inspire us
Pharmaceutical-scientific university degree or comparable. You bring 2-3 years of experience in Quality in the pharmaceutical sector and are familiar with GMP/GDP. You are an open, friendly, reliable and competent personality with individual responsibility and assertiveness. You appreciate dealing with customers and authorities, prioritize and like to work independently. As a team player, you have good communication and organizational skills. You have a "hands-on" mentality and are characterized by a systematic, exact and service-oriented way of working.
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. 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?
Send your complete application dossier and discover how you can move forward with us. jpid37d6dbdjm jit0834jm jiy26jm
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