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 PAYESenior Regulatory Specialist Role:Lead the development and execution of regulatory strategies in the UK and IrelandBe the local regulatory contact for MHRA and HPRA on assigned productsLead post-approval product information managementDrive departmental readiness for audits, inspections, and procedural compliance activitiesLead post-approval product information managementYour 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 industryKnowledge of EU, UK and Irish regulatory processes, GxP and quality systemsExperience with regulatory information management (RIM) systems such as Veeva Vault or similarStrategic thinker with strong analytical, problem-solving, and decision-making skillsCompany: 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