Beschreibung
For a Swiss pharmaceutical company that develops, manufactures drugs for treating rheumatic diseases, accident and sport injuries, venous and vascular complaints, as well as dermatologies and gynecological disturbances I'm looking for a Regulatory Affairs Freelancer in the Basel Area.Duties and responsibilities:
- Provide of registration dossiers for the in-house made RX- and OTC- products (Modules 1-5)
- Transformations of existing registration dossiers into the CTD-Format
- Mentoring and update of existing submissions
- Be the company's representative for the products to regulatory agencies and bodies.
- Support the Director of RA in international Projects (EU, Asia,Russia)
YOU'RE PROFILE:
- You have a scientific or medical degree ideally in the pharmaceutical or natural science
- Proven experience with submissions of drugs in Switzerlandand EU
- Fluent English and German - both written and spoken
- French is a benefit
- Excellent communication and negotiation skills
Project Details
- Freelancer Position
- For 6 Months and a Option of extension
- 60-100 % onside
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.
Kristina Bröckel
Regulatory Affairs Consultant
Tel:
mailto:
To find out more about Real Staffing please visit www.realstaffing.com