Description
Regulatory Affairs Manager - Switzerland - 1 year contractOur client, a global science-based company active in health, nutrition and materials is currently seeking for a Regulatory Affairs Manager. As Regulatory Affairs Manager you are going to be responsible for the product approvals and maintenance of compliance in the different pharma markets for Europe Middle East and Africa. You also are going to support Marketing and Sales in all regulatory and quality related issues
Requirements
- 3-5 years of expertise in Regulatory Affairs
- A degree in the life sciences, post-graduate is preferred but not required
- Proven experience with European regulatory procedures
- Knowledge on regulations and standards for DNP and DFS business
- Experience with Active Pharmaceutical Ingredients (API's)
- English is a must, German would be an advantage
- Excellent communicator, both verbal and written
- Valid Swiss Work Permit
Duties and Responsibilities will include
- Preparing and coordinating regulatory documentation
- Collecting and collating a wide range of information
- Responsible for global or regional representation
- Supporting TQM for the product specifications in customer Quality agreements
I am a specialized recruiter, currently taking care of various projects within the Regulatory Affairs area in Switzerland. For more information about this role or jobs within related specialist areas please send me your CV as a Word document with your hourly rate expectation for immediate consideration.
You can reach me on or (a.xenitidis'at'realstaffing.com)
Keywords: Regulatory Affairs Manager, Swissmedic, Switzerland, DMF, API, English, TQM, DNP, DFS, biology, toxicology