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For Companies At a Glance
- Tasks: Lead regulatory strategies and manage product information for a global pharmaceutical company.
- Company: Join a leading firm dedicated to improving patient health worldwide.
- Benefits: Competitive pay at £24.50 per hour, with opportunities for professional growth.
- Other info: Dynamic role with potential for career advancement in a supportive environment.
- Why this job: Make a real difference in healthcare while developing your regulatory expertise.
- Qualifications: Degree in a scientific field or relevant experience in regulatory affairs.
The predicted salary is between 48000 - 52000 £ per year.
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
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. 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.
Senior Specialist in London employer: Talentmark
Contact Detail:
Talentmark Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Specialist in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who have experience with regulatory affairs. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of UK and Irish regulatory processes. We recommend creating a list of common interview questions related to regulatory strategies and practising your answers to show off your expertise.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values. Check out our website for roles that excite you, and tailor your approach to highlight how you can contribute to their mission of putting patients first.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can keep you top of mind. Use this opportunity to reiterate your enthusiasm for the role and mention something specific from the interview that resonated with you.
We think you need these skills to ace Senior Specialist in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Regulatory Specialist role. Highlight your relevant experience in regulatory affairs and any specific knowledge of UK and Irish processes. We want to see how your background aligns with what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for this role. Mention your strategic thinking and problem-solving skills, and don’t forget to show your passion for putting patients first, just like we do at StudySmarter.
Showcase Your Experience with RIM Systems: If you've worked with regulatory information management systems like Veeva Vault, make sure to highlight that experience. We love seeing candidates who are familiar with the tools that help streamline regulatory processes!
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It helps us keep everything organised and ensures your application gets the attention it deserves. Don’t miss out on this opportunity!
How to prepare for a job interview at Talentmark
✨Know Your Regulations
Make sure you brush up on the latest EU, UK, and Irish regulatory processes. Being able to discuss specific regulations and how they apply to the role will show that you're not just familiar with the basics but are genuinely invested in the field.
✨Showcase Your Experience
Prepare to talk about your previous roles in regulatory affairs, especially any experience with RIM systems like Veeva Vault. Use specific examples to illustrate how you've successfully navigated regulatory challenges in the past.
✨Be Audit-Ready
Since this role involves driving departmental readiness for audits and inspections, be ready to discuss your experience with compliance activities. Highlight any past experiences where you ensured procedural compliance or led a team through an audit.
✨Think Strategically
Demonstrate your strategic thinking skills by discussing how you approach problem-solving in regulatory scenarios. Prepare a couple of examples where your analytical skills made a significant impact on a project or decision.