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Regulatory Affairs and Quality Manager 60-80%
Vor 7 Tagen
**Beschreibung**
In this role, you will ensure compliance with regulatory requirements in the markets. You will be responsible for the preparation of documentations in collaboration with manufacturers, the processing of new submissions and the logistics chain related to the marketing authorisation of medicinal products. You will also have legal responsibility for the entire quality management process (qualification of manufacturers, release of batches for distribution, management of the quality management system, product quality reviews, audits and assurance of good distribution practices in the supply chains). You will be the point of contact for all quality issues, both for manufacturers and partners and for customers in the markets.
**Motivation**
Centrally located workplace in Winterthur. Modern infrastructure. Flexible working hours. Flat hierarchies. 5 weeks' holiday. Generous home office arrangements. Expandable scope of responsibility. International and friendly work environment.
**Firmenprofil**
A successful Swiss pharmaceutical company.
**Spezielles**
**Erfahrung**
This challenging role requires several years' experience in regulatory affairs. You also have very good English and French skills, ideally good German skills. We are looking for a conscientious and independent personality who is able to work solution
- and goal-oriented. As a team player with good communication skills and an open mind, you will be a perfect fit in our international team.
**Ausbildung**
Master's degree in a scientific discipline or commercial training with additional training in business administration
**Sprachen**
Deutsch: Preferred
Englisch: Very good
Französisch: Good
**Arbeitsort**
Winterthur
**Arbeitsbeginn**
By agreement
**Vakanz-Nummer**
P-1-31674
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