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Regulatory Affairs Specialist 
Location: Switzerland
Salary: Competitive SF 

Are you looking for an exciting opportunity and have a passion for working within Regulatory Affairs? An excellent opportunity has arisen with a global eye care company based in Switzerland.


•Coordination and submission of marketing authorisation applications
•Handle quality complaints, incidents and other safety related reports
•Product labelling
•Coordinate and prepare submissions
•Maintain marketing authorisation of medicinal products
•Comply with legal, internal and division requirements
•Generate reports
•Coordinate, prepare and submit clinical trial applications
•Establish and reverse documents in the Regulatory Affairs processes

Qualifications/experience required:

•A degree in Pharmacy, medicine, biology, biochemistry or chemistry
•Fluent English and German skills + Good knowledge in written and spoken French
•Have at least 3 years experience in Regulatory Affairs from Pharmaceutical or medical devices industry
•Knowledge in Swiss Health regulations, vigilance, marketing authorisation and clinical trials

If you are interested please contact:

Jim Maddison on +44 (0) 0207 822 1717 or 

If however, you do not feel that this is the right role for you, please forward these details on as we have a generous referral scheme in place.
Please note due to the high level of applications if you are not contacted within 48 hour, you have not been successful on this occasion.

Key Words: Regulatory Affairs, Submissions, Pharmacy, Medicine, Biology, Biochemistry, Chemistry, French, German, English, Complaints, Reports, Clinical Trials, Pharmaceutical and Medical Devices

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