Pharmacovigilance and Quality Assurance Manager

1 day ago


Surrey, United Kingdom Zentiva Group Full time
Role Summary

This Pharmacovigilance and Quality Assurance Manager position is a vital part of our Scientific Affairs department in Zentiva UK. The successful candidate will oversee PV case management, author and maintain the UK pharmacovigilance system master file (PSMF), and act as the primary PV contact person for the MHRA.

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 Group

Zentiva is a well-established pharmaceutical company dedicated to delivering 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 strive to create a balanced team across the company and welcome applications from all qualified candidates regardless of their educational and industry experiences, cultural or ethnical backgrounds, and different life experiences or abilities.

Key Responsibilities
  • Act as the UK National Contact Person for Pharmacovigilance (NCPP).
  • Maintain oversight of all UK PV cases (including cases received via health authorities).
  • Author and maintain the UK pharmacovigilance system master file (PSMF).
  • Ensure that the UK Qualified Person for pharmacovigilance (QPPV) is kept fully aware of all UK PV specific information.
Benefits Package

We offer a comprehensive benefits package, including a competitive salary of approximately £65,000 per annum, international working environment, passionate team of professionals, and continuous learning & development opportunities thanks to our Zentiva Academy.



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