

ROLE OVERVIEW
We are currently looking for a Regulatory Affairs Specialist to join a leading organisation within the life sciences sector based in the UK. This is an exciting opportunity for an experienced professional to contribute to the management of regulatory compliance and product submissions within a dynamic team.
An ideal candidate will play a key role in ensuring our client’s products meet all necessary regulatory standards, supporting new product launches and maintaining ongoing compliance across diverse markets. This role offers a chance to develop your expertise within a forward-thinking environment committed to innovation and excellence.
KEY DUTIES AND RESPONSIBILITIES
Your duties as the Regulatory Affairs Specialist will be varied however the key duties and responsibilities are as follows:
- To oversee regulatory submissions and maintain accurate documentation to ensure compliance with local and international regulations.
- To collaborate with cross-functional teams including R&D, quality assurance, and manufacturing to support regulatory strategies.
- To monitor changes in regulatory requirements and update internal processes accordingly.
- To provide guidance and support on regulatory issues and documentation for product lifecycle management.
- As the Regulatory Affairs Specialist you will ensure ongoing compliance and contribute to the successful approval of new and existing products.
ROLE REQUIREMENTS
To be successful in your application to this exciting role as the Regulatory Affairs Specialist we are looking to identify the following on your profile and past history:
- A Degree or higher level in a relevant field (e.g., Pharmaceutical Chemistry / Quality Assurance / Regulatory Affairs).
- Proven experience in a regulatory affairs role within the life sciences or pharmaceutical industries, demonstrating knowledge of regulatory procedures and submissions.
- Strong communication skills, with the ability to liaise effectively with regulatory authorities and internal teams.
WHAT’S IN IT FOR YOU?
Joining our client means being part of an innovative organisation that values professional growth, offers competitive benefits, and fosters a collaborative environment. It’s a fantastic chance to advance your career in a vital role within the regulatory landscape and make a real impact within the industry.
Key Words: Regulatory / Compliance / Submissions / Life Sciences / Pharmaceutical / Quality Assurance / Product Lifecycle / International Regulations / Team Collaboration
"Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career".
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.


