Regulatory Affairs Associate

CK Group are recruiting for a Regulatory Affairs Associate to join a leading global helathcare company on a contract basis until December 2026. This is a hybrid role with 2 days per week in Reading.

Salary:

From £25 ph PAYE

Regulatory Affairs Associate Role:

• Support and maintain pharmaceutical product portfolios
• Manage ongoing product information updates
• Supports regulatory project plan execution
• Assist in the preparation and review of labelling and local SOPs
• Compile regulatory documents for submission

• Hold a relevant scientific degree or have equivalent working experience
• Good knowledge and experience of UK

  regulations

• Previous working experience in pharmaceutical regulatory affairs
• Ability and experience to work cross-functionally with different functions involved: Global functions, QA, PV, Marketing
• Excellent communication skills
• Any project management experience would be an advantage

Our client is one of the worlds leading healthcare providers, and has been highly innovative in providing healthcare solutions, to unmet medical needs through scientific advancement as well as strategic acquisitions and partnerships. They work at the critical intersection where innovations that save and sustain lives meet the physicians, nurses and pharmacists who make it happen. Our client is committed to improving outcomes for patients, and helping their partners meet the evolving challenges and opportunities in healthcare around the world.

Apply:

For more information, or to apply for this Regulatory Affairs Associate

please contact the Key Accounts Team on 01438 870011 or email [email protected]. Please quote reference 173 158.

It is essential that applicants hold entitlement to work in the UK

Please note:

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