Regulatory Affairs Manager

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Regulatory Affairs Manager

Malmö

You will have a broad area of responsibility within quality assurance, pharmacovigilance, regulatory affairs and medical information and report to our Nordic Head of Scientific Affairs. The responsibilities could for some areas include all Nordic countries, as we are presently integrating our Nordic operations.

The primary responsibilities

Quality assurance including production of various types of documentation (standard operating procedures, enclosures, work instructions etc.), self-inspections, participation in audits and follow up
Reporting of adverse events, (SCP)
National documentation of EU processes and translations of documents

Check the job satisfaction:

267 ratings

Published: 16-04-2015