Regulatory Affairs Coordinator (m/w/d)

Description

In this position you are responsible for the management of the RA-owned procedural documents and mandatory training for RA worldwide. Your activities include: - Ensure updated and compliant status of RA-owned procedural documents (tracking and coordination of writing) - Support the RA SOPs authors with training and continuous guidance / operational help - Manage training assignment of SOPs /WIs to relevant roles in RA, and maintain RA training curricula information - Support the RA GDD organization for internal global audits related to SOPs and training - Help to devise and implement relevant remedial and improvement actions for Corrective Action Plans from training audits and follow-up on completion and implementation of relevant tasks to ensure closure

Motivation

Are you looking to work in a global growth company where you can make a real difference? Then you are right with us!

Company description

Globally & successfully operating company within the pharmaceutical industry.

Special

If you are interested then kindly send your resume to: a.ahanor@universaljob.ch

Experience

5 years Pharmaceutical working experience with preferably experience in Regulatory Affairs and Basic knowledge of global regulatory requirements.

P-13-7403