Description
Regulatory Affairs Manager (m/f)
Reference: -en
Start: asap
Duration: 6 MM
Main tasks:
- Support Regulatory Affairs Life Cycle Management (RA LCM) Europe team
- Develop RA LCM related policies, and implement their flawless execution with leadership, and developing strong partnership with relevant interfaces
- Organize the transfer of food supplement dossiers as well as the responsibilities and product know-how into RA LCM group
- Organize the transfer of medicinal products as well as the responsibilities and product know-how into RA LCM group
- Implement and supervise a sustainable and cost efficient outsourcing strategy
- Prepare and submit dossiers for registration and compliance and to achieve registrations for the specific product portfolio
Main qualifications
- Know-how of regulatory environment for food supplements and medicinal products
- Development and preparation of successful regulatory strategies
- Experience in working across a wide range of regulatory systems and databases
- Project management know-how
- Strong experience in business development responsibilities
- Solid experience with OTC environment
- Strong experience with LCM activities
- English and German (business fluent)
Main advantages:
- A very renowned company
About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
My contact at Hays:
My contact person:
Esat Yaktubay
Referencenumber:
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