Senior Specialist

Talentmark are recruiting for a Senior Regulatory Specialist

to join a global pharmaceutical company on a contract basis for 12 months.

Salary:

£24.50 ph PAYE

Senior Regulatory Specialist Role:

• Lead the development and execution of regulatory strategies

  in the UK and Ireland

• Be the local regulatory contact for MHRA and HPRA on assigned products
• Lead post-approval product information management
• Drive departmental readiness for audits, inspections, and procedural compliance activities
• Lead post-approval product information management

Your Background:

• Hold a degree in a relevant scientific subject or have equivalent working experience

• Some work experience in a regulatory affairs role in the pharmaceutical industry
• Knowledge of EU, UK and Irish regulatory processes, GxP and quality systems
• Experience with regulatory information management (RIM) systems such as Veeva Vault or similar
• Strategic thinker with strong analytical, problem-solving, and decision-making skills

Company:

Our client is the global leader in enabling pharma, biotech, and consumer health partners to optimize product development, launch, and full life-cycle supply for patients around the world. They have the goal of putting patients first and to help people around the world live better and healthier lives.

Apply:

For more information, or to apply for this Senior Regulatory Specialist

please contact the Key Accounts Team on 01438 870011 or email pharmacontracts@talentmark.co.uk. Please quote reference 182 875.

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.