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Regulatory Affairs Manager

  1. East Anglia
  1. Contract
  1. Drug Safety / Pharmacovigilance
Date Posted06 Sep 2019
Our client is one of the world’s leading biotechnology companies.  Our client is a values-based company, deeply rooted in science and innovation to transform new ideas and discoveries into medicines for patients with serious illness.
They strive to serve patients by transforming the promise of science and biotechnology into therapies that have the power to restore health or save lives. In everything that they do, they aim to fulfill their mission to serve patients.

They are looking for a Regulatory affairs manager to lead regulatory projects for emerging markets commercialisation and life cycle management of assigned products.

Responsibilities include:

- organization and preparation CMC investigational product amendments and post-market supplements
- organization and preparation CMC sections of annual reports 
- GMP registration of facilities
- Providing guidance on regional regulatory mechanisms to optimise product registration 

If this seems like something you wish to get involved in or hear more about, apply today! 

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