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 (phone number removed) or email (url removed). Please quote reference (Apply online only).
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