Regulatory Affairs Coordinator

Regulatory Affairs Coordinator wanted for our Zug based client in the pharmaceutical sector.

YOUR EXPERIENCE/SKILLS:

- BSc or MSc in Pharmacy, Life Science or similar
- At least 2 years of experience in a relevant field
- The ability to accomplish tasks in the required quality on time
- Know how in databases and archives
- Languages: fluent English and German both written and spoken, intermediate French and intermediate Italian knowledge would be a plus

YOUR TASKS:

- Coordinating and preparing high quality submissions of regulatory dossiers for assigned products to Swissmedic in time
- Being responsible for regulatory maintenance activities such as CMC variation, safety updates and annual reports
- Managing printed text material according to the quality standards and timelines set by Swissmedic and other stakeholders as well as involving relevant global and local functions
- Communicating and tracking regulatory, relevant activities and commitments as well as maintaining country specific information in databases and archives
- Ensuring traceability and integrity of current and past DRA records for Switzerland by accurate and timely data management in regulatory compliance databases for assigned products
- Establishing and maintaining a close professional relationship to Swissmedic

START: 01/2017

DURATION: 3MM++

Location: Zug, Switzerland

Ref.Nr.: BH10130

Does that sound interesting?

Does that sound like a challenging opportunity to you?

Then take the next step and send us your CV as a Word Document and a daytime contact telephone number.

DUE TO WORK PERMIT RESTRICTIONS WE CAN UNFORTUNATELY ONLY CONSIDER APPLICATIONS FROM EU OR SWISS CITIZENS AS WELL AS CURRENT WORK-PERMIT HOLDERS FOR SWITZERLAND.

GOING THE EXTRA MILE

NEW TO SWITZERLAND?

In case of successful placement, we support you with:

- All administrative questions
- Finding an apartment
- Health - and social insurance
- Work permit and much more