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- Tasks: Lead regulatory efforts for cutting-edge stem cell therapies and engage with key stakeholders.
- Company: Dynamic therapeutics company focused on advanced therapies in London.
- Benefits: Highly competitive day rate and potential for long-term engagement.
- Why this job: Make a real impact in the exciting field of cell and gene therapy.
- Qualifications: Experience in ATMPs and strong regulatory background required.
- Other info: Hybrid work model with immediate start and excellent growth opportunities.
The predicted salary is between 50000 - 65000 £ per year.
Location: London (hybrid)
Engagement: Full-time consulting for 3 months initially, then a long-term arrangement
Sector: Cell Therapy | Stem Cells | GMP | Advanced Therapies
Regulatory Bodies: MHRA | CQC
We are supporting a therapeutics company that is preparing to launch an advanced stem cell therapy platform. They are now seeking an experienced Regulatory Consultant to step in immediately and take ownership of regulatory remediation and stakeholder engagement.
- Act as the primary regulatory lead and interface with MHRA
- Stabilise the regulatory position following inspection feedback
- Build, formalise and implement GMP and regulatory processes
- Strong background in ATMPs / autologous stem cell therapies
- CQC experience is highly desirable
Start: ASAP
Format: Full-time consulting role
Day rate is highly competitive (budget approved)
The right individual will be engaged immediately.
Regulatory Consultant – Cell & Gene Therapy in London employer: Valtera Group Ltd
Contact Detail:
Valtera Group Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Consultant – Cell & Gene Therapy in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the cell and gene therapy space. Attend industry events or webinars to meet potential employers and get your name out there.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ATMPs and regulatory processes. We want you to be able to discuss your experience confidently and show how you can stabilise regulatory positions.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your expertise in GMP and CQC. Use our website to find roles that match your skills and interests, making your application stand out.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can keep you top of mind for hiring managers. Show them you're keen and ready to take ownership of regulatory challenges.
We think you need these skills to ace Regulatory Consultant – Cell & Gene Therapy in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to highlight your experience in regulatory affairs, especially in ATMPs and stem cell therapies. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant projects!
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 experience with MHRA and CQC, and how you can stabilise regulatory positions after inspections. Let us know what makes you tick!
Showcase Your Stakeholder Engagement Skills: Since stakeholder engagement is key for this role, make sure to include examples of how you've successfully managed relationships in previous roles. We love to see how you’ve navigated complex regulatory landscapes!
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 Valtera Group Ltd
✨Know Your Regulatory Stuff
Make sure you brush up on your knowledge of ATMPs and the specific regulations surrounding cell and gene therapy. Familiarise yourself with the MHRA and CQC guidelines, as you'll need to demonstrate your expertise in these areas during the interview.
✨Showcase Your Experience
Prepare to discuss your previous roles and how they relate to regulatory remediation and stakeholder engagement. Be ready to share specific examples of how you've stabilised regulatory positions or implemented GMP processes in past projects.
✨Engage with Confidence
Since you'll be acting as the primary regulatory lead, it's crucial to convey confidence in your ability to interface with regulatory bodies. Practice articulating your thoughts clearly and assertively, as this will help build trust with the interviewers.
✨Ask Insightful Questions
Prepare a few thoughtful questions about the company's current challenges and future plans regarding their stem cell therapy platform. This shows your genuine interest in the role and helps you understand how you can contribute effectively.