Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead global regulatory strategies for cutting-edge cell and gene therapies.
- Company: Join a leading CDMO known for advanced therapies and biologics.
- Benefits: Executive visibility, direct client partnerships, and influence in innovative life sciences.
- Why this job: Shape the future of healthcare by driving regulatory excellence in a dynamic environment.
- Qualifications: Degree in Life Sciences and extensive regulatory affairs experience required.
- Other info: Be part of a high-performing team with opportunities for professional growth.
The predicted salary is between 72000 - 108000 £ per year.
ROLE OVERVIEW An exciting opportunity for a VP, Global Regulatory Affairs to join a leading Cell and Gene Therapy CDMO. As the VP, Global Regulatory Affairs, you will play a key role in providing global regulatory leadership, supporting clients developing advanced therapy programmes from early development through to commercialisation. You will be responsible for defining and implementing global regulatory strategies, ensuring compliance with international standards, and building strong partnerships with regulatory authorities. This role reports directly into the SVP, Global Quality and will lead an experienced regulatory team during a period of continued international growth. KEY DUTIES AND RESPONSIBILITIES Your duties as the VP, Global Regulatory Affairs will be varied however the key duties and responsibilities are as follows: Develop and execute global regulatory strategies that support client programmes across cell and gene therapy, ensuring alignment with regional and international agency expectations. Act as the senior regulatory representative with global health authorities, leading discussions, responses, and inspections while building trusted long-term relationships. Provide expert regulatory input across CMC, clinical, and post-approval activities, supporting high-quality submissions such as INDs, IMPDs, and variations. Partner with commercial, quality, and technical operations teams to provide regulatory insight during client engagements, business development activities, and due diligence reviews. Lead, coach, and mentor a high-performing global regulatory team, fostering collaboration, accountability, and professional development across regions. ROLE REQUIREMENTS To be successful in your application to this exciting role as the VP, Global Regulatory Affairs we are looking to identify the following on your profile and past history: A Degree or higher level in a relevant Life Science discipline (e.g., Pharmaceutical Chemistry / Biochemistry / Regulatory Science). Extensive experience in global regulatory affairs within biologics, advanced therapy, or gene therapy environments. Proven leadership experience within a CDMO or partnering organisation, managing regulatory teams and engaging with global health authorities. Demonstrated ability to lead strategic regulatory initiatives, ensuring compliance and supporting clients through the product lifecycle. WHAT’S IN IT FOR YOU? You will join a business recognised for its expertise in advanced therapies and biologics manufacturing, with the opportunity to shape global regulatory strategy across a growing international network. This position offers visibility at executive level, direct involvement in client partnerships, and the chance to influence regulatory direction in one of the most innovative areas of life sciences. You will be part of the senior leadership team driving excellence in Cell and Gene Therapy development. KEY WORDS: VP Global Regulatory Affairs / Regulatory Affairs / Advanced Therapy / Gene Therapy / Biologics / ATMP / CGT / CDMO / CMC / FDA / EMA / MHRA / Leadership / Compliance / Regulatory Strategy / Quality Systems / Biotechnology Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career
VP Global Regulatory employer: Hyper Recruitment Solutions LTD
Contact Detail:
Hyper Recruitment Solutions LTD Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land VP Global Regulatory
✨Network Like a Pro
Get out there and connect with people in the industry! Attend conferences, webinars, or local meetups related to regulatory affairs. Building relationships can open doors and give you insider info on job opportunities.
✨Showcase Your Expertise
When you get the chance to chat with potential employers, don’t hold back! Share your insights on global regulatory strategies and your experience with health authorities. This will show them you’re not just another candidate, but a valuable asset.
✨Leverage Social Media
Use platforms like LinkedIn to highlight your achievements and connect with industry leaders. Join relevant groups and participate in discussions to increase your visibility and demonstrate your knowledge in regulatory affairs.
✨Apply Through Our Website
Don’t forget to check out our website for the latest job openings! Applying directly through us not only shows your interest but also gives you a better chance of being noticed by our hiring team.
We think you need these skills to ace VP Global Regulatory
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the VP, Global Regulatory role. Highlight your experience in global regulatory affairs and any leadership roles you've held. We want to see how your background aligns with the key duties and responsibilities outlined in the job description.
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 specific experiences that demonstrate your ability to lead regulatory strategies and build relationships with health authorities. We love a good story!
Showcase Your Achievements: Don’t just list your responsibilities; showcase your achievements! Use metrics or examples to illustrate how you’ve successfully navigated regulatory challenges or led teams to success. This will help us see the impact you've made in your previous roles.
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It helps us keep track of your application and ensures you’re considered for the role. Plus, it’s super easy to do!
How to prepare for a job interview at Hyper Recruitment Solutions LTD
✨Know Your Regulatory Landscape
Before the interview, brush up on the latest regulations and guidelines from global health authorities like the FDA, EMA, and MHRA. Being able to discuss recent changes or trends in regulatory affairs will show your expertise and commitment to staying informed.
✨Showcase Your Leadership Skills
Prepare examples of how you've successfully led regulatory teams in the past. Highlight specific instances where you mentored team members or navigated complex regulatory challenges. This will demonstrate your ability to lead and inspire a high-performing team.
✨Align with Company Values
Research the company’s mission and values, especially their focus on advanced therapies and biologics. Be ready to articulate how your personal values align with theirs and how you can contribute to their goals in the cell and gene therapy space.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your problem-solving skills in regulatory affairs. Think about potential challenges you might face in this role and how you would approach them. This will showcase your strategic thinking and readiness for the position.
