Regulatory Affairs Manager

  • Salary: £0 - £61 per hour
  • REF Number: v-107872
  • Consultant: Key Accounts Team
  • Contact: 01438 870011
  • Date Published: 15.10.2024
  • Industry: Pharmaceutical
  • Location: High Wycombe, Buckinghamshire, England
  • Functional Expertise: Regulatory Affairs

CK Group are recruiting for a Regulatory Affairs Manager, to join a company in the Pharmaceutical industry, at their site based in High Wycombe, on a contract basis to the end of March 2025.

Salary:

Hourly £61.00 per hour PAYE or £82.00 per hour Umbrella.

 

Regulatory Affairs Manager Role:

Management of post-approval activities for specified OTC products

  • Supports the EMEA Regulatory Affairs team for post-approval activities for MRP/DCP products across EEA and coordinate worksharing (WS) procedures for CMC and non-CMC variation, when WS is appropriate.
  • Development of regulatory strategies, preparation of regulatory applications and support maintenance activities for MRP/DCP products.
  • Supports the team with regulatory activities for European procedures (Decentralised, Mutual Recognition, WS) as appropriate.
  • Supports the team with regional regulatory strategies in line with business plan for post-approval activities.
  • Supports the team to complete identified regulatory activities to ensure all regulatory obligations and business objectives are met.
  • Prepares and compiles regulatory submissions (Variations, renewals, PSUSA etc.), responses to Regulatory Agency (RA) questions and other correspondence in accordance with EU regulations and guidelines.
  • Ensure Marketing Authorisations are maintained and renewed.

Your Background:

  • Life sciences or chemistry graduate to honours level or equivalent.
  • Works with minimal supervision to plan, conduct, and manage regulatory submissions for European procedures and multiple projects to meet department and company objectives.
  • Work with minimal supervision to determine and develop approaches to solutions with technical guidance on a variety of problems of moderate scope and complexity.
  • Project management, understanding of regulatory environment, interaction with the Regulatory Authorities (as appropriate), commercial / strategic awareness, implement regulatory strategy, managing and maintaining Marketing Authorisations etc.

Company:

Our client is the largest and most broadly-based healthcare company. They strive to improve access and affordability, create healthier communities, and put a healthy mind, body and environment within reach of everyone, everywhere.

Location:

This role is hybrid working with 2/3 days per week based in High Wycombe.

Apply:

It is essential that applicants hold entitlement to work in the UK. Please quote job reference 107 872 in all correspondence.

Please note: 

This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

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