Regulatory Affairs and Scientific Information Expert

2 days ago


Surrey, United Kingdom Zentiva Group Full time
Scientific Information Expert Role

This Regulatory Affairs and Scientific Information Expert role is a critical part of our Scientific Affairs department in Zentiva UK. The successful candidate will lead the building of a motivated and engaged team through the use of formal and informal recognition, regular communications, and the encouragement of cooperation between individuals and teams.

The ideal candidate will have a life science degree or a qualified health professional background with at least 5-10 years' experience in pharmacovigilance and previous line management responsibilities.

About Zentiva UK

Zentiva is a leading pharmaceutical company that strives to deliver high-quality medicine to people whose lives depend on it. Our mission is to create a work culture where everyone feels appreciated, valued, and empowered to contribute their best.

We welcome applications from all qualified candidates regardless of their educational and industry experiences, cultural or ethnical backgrounds, and different life experiences or abilities.

Main Responsibilities
  • Lead and participate in any UK PV inspections and audits.
  • Manage the pregnancy prevention programs for Thalidomide and Lenalidomide and any other products requiring pregnancy prevention programs marketed in the UK or Ireland.
  • Represent the UK PV department internally and externally at a global level and function as an authoritative and professional member of the Scientific Affairs team.
Benefits

We offer a competitive salary of approximately £70,000 per annum, international working environment, passionate team of professionals, and continuous learning & development opportunities thanks to our Zentiva Academy.



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