Regulatory Consultant

Description

Regulatory Consultant

Location: Basel, Switzerland

Length of the contract: contract until end of year, with a huge chance to be extended for another year.

Rate: market rate

Company:

Our client, an international pharmaceutical company, is currently looking for a Regulatory Affairs Consultant to work on their Site in the Basel area to overview its licence transfer.

The Regulatory Affairs manager will be in charge of the Regulatory Affairs matters on regional and and Europe site base.

Furthermore, our client is expecting the candidates to have at least 3-5 years of experience in

Regulatory Affairs. Animal Health knowledge would be of advantage

We have already agreed on interviews.

The ideal start date is as soon as possible.
In regards to the workload, we are looking for someone who is available ideally 5 days a week, with the possibility of 20% home office.

Responsibilities:

-License transfers (company to other international enterprise)

-POC to HA (EMEA and Swissmedic)

-Responsible for all documentation

-Responsible for manufacturing licenses (required from CMO)

Requirement:

-A minimum of 3-5 years of experience in RA Pharma or related industries.

-Swiss medic experience

-EMEA experience

-Sound GMP knowledge

Required application documents:

• Updated CV including requested experience/responsibilities as per above

• 5-10 bullet points with relevant experience

• 2 reference contact persons, will be required at interview stage

• Your start date, required rate and interest.

I am looking forward to hear from you.

Bests,

Sabina Keel

Realstaffing Schweiz, Pharma, Biotech & Medical Devices

Talstrasse 65, Zurich, 8001, Switzerland

T:

E: