Pharmaceuticals

Senior Manager of Safety Information

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About the job

  • UK

Do you have significant experience within regulatory affairs – specifically safety information and/or compliance? Are you interested in stepping into a more senior position in a global pharmaceutical company specialising in generics?

Invenia Group is currently partnered with a leading international pharmaceutical company, who are seeking a Senior Manager of Safety Information. This professional will manage all regional and local Regulatory Affairs activities related to Pharmacovigilance. This is a fully remote role and open to applicants who currently reside in the UK and have right-to-work.

Role responsibilities:

If successful, as the Senior Manager of Safety Information, you will maintain the product information, quality, and accuracy as well as handle all the pre-licensing product safety information submissions throughout the EMENA region. You will also handle all product safety-related post-licensing activities and review outcomes of PSUSA/PRAC procedures.

What we are looking for:

An ideal candidate would hold a life science degree and have extensive experience within Pharmaceutical Regulatory Affairs. You must have great working knowledge of EU post-approval submissions and possess the ability to work within the realm of safety variations. You will also have a great working-knowledge of PV regulations and guidance in the area of Regulatory Affairs.

This is a great opportunity to join a growing team within an industry-leading generics company promising further growth plans. It is an unusual role combining Regulatory Affairs alongside Pharmacovigilance responsibilities which will further develop your skillset and professional horizons.

If you are interested in proceeding with this opportunity, please apply so we can arrange a confidential discussion to discuss the position in more detail.