Regulatory Affairs Specialist with Pharmaceutical Expertise

1 day ago


High Wycombe, Buckinghamshire, United Kingdom CK Group Full time

Are you a seasoned regulatory affairs professional looking for a new challenge in the pharmaceutical industry? We have an exciting opportunity for a Regulatory Affairs Manager to join our client, a leading healthcare company based in High Wycombe.

About the Role

This is a contract-based position that will see you working on post-approval activities for specified OTC products. You will be responsible for managing post-approval activities, developing regulatory strategies, and preparing regulatory applications. Your expertise in European procedures and commercial awareness will also be valuable assets in this role.

We are looking for someone who can work independently to plan, conduct, and manage regulatory submissions for European procedures and multiple projects. If you have a strong understanding of the regulatory environment and excellent project management skills, we want to hear from you

Requirements
  • A degree in life sciences or chemistry to honors level or equivalent
  • Strong knowledge of European regulations and guidelines
  • Ability to determine and develop approaches to solutions with technical guidance
  • Commercial / strategic awareness and ability to implement regulatory strategy
About Our Client

Our client is a global healthcare company that strives to improve access and affordability, create healthier communities, and put a healthy mind, body, and environment within reach of everyone, everywhere. They offer a hybrid working arrangement with 2/3 days per week based in High Wycombe.

What We Offer

As a Regulatory Affairs Manager at our client, you can expect a competitive salary of £61.00 per hour (PAYE) or £82.00 per hour (Umbrella), making it an attractive option for those looking for a rewarding career in the pharmaceutical industry.



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