Beschreibung
I am looking for regulatory affairs freelancers for multi-faceted Projects in Pharmacy, Medical Device, Biology, Cosmetics and Chemistry in beautiful areas of Switzerland.Your duties and responsible:
- Covering the whole product's life cycle
- RA and registration (premarket activities)
- Post market activities
- Regulatory strategy
- You will be providing regulatory support to all areas of the business
- You will have the chance to determine submission strategies and registration dossier
- You will also be the knowledgeable person for EU, US and international regulations
- You will also be the company's representative for your specific products to regulatory agencies and bodies
Requirements
- English (French and German are a benefit)
- previous RA experience at least min. 2 years
- Scientific/engineering background (PhD. is a benefit)
- Experience as a Consultant / Freelancer
For a confidential discussion about regulatory affairs projects in Switzerland, or to apply, then send your CV to or call me.
I am a specialist recruitment consultant in regulatory affairs for the Pharmaceutical & Biotechnology industry. I offer a number of search options within the industry with a special focus on Switzerland.
If you are a Pharmaceutical professional looking for your next opportunity, then please don't hesitate to get in contact with me. Alternatively if you are currently looking for skilled individuals for the development of your organisation, then I can certainly help.
Your personal contact:
Kristina Bröckel
Regulatory Affairs Consultant
Tel:
mailto:
Specialties
Regulatory Affairs Contractors, Project Manager, Submissions Specialist, CMC, CTA, Freelancers, Generics, Cosmetics, Prescription Drugs, Bio-tech, Biologics, Medical Devices.
To find out more about Real Staffing please visit www.realstaffing.com