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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, hybrid work model, and potential for long-term engagement.
- Why this job: Make a real difference in the innovative field of cell and gene therapy.
- Qualifications: Experience in ATMPs and strong regulatory background required.
- Other info: Immediate start with opportunities for professional growth.
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 Slough 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 Slough
✨Tip Number 1
Network like a pro! Reach out to your connections in the cell and gene therapy sector. 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 regulatory bodies like MHRA and CQC. Show them you know your stuff and can handle the complexities of ATMPs with ease.
✨Tip Number 3
Don’t just wait for job postings; be proactive! Reach out directly to companies you admire, especially those working on advanced therapies. A little initiative can go a long way.
✨Tip Number 4
Apply through our website for the best chance at landing that role. We’re always looking for passionate individuals who want to make a difference in the field of cell therapy!
We think you need these skills to ace Regulatory Consultant – Cell & Gene Therapy in Slough
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Regulatory Consultant role. Highlight your experience with ATMPs and any relevant regulatory bodies like MHRA and CQC. We want to see how your background aligns with our needs!
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. Share specific examples of your past work in regulatory remediation and stakeholder engagement that relate to cell and gene therapy.
Showcase Your Expertise: Don’t hold back on showcasing your expertise in GMP and regulatory processes. We’re looking for someone who can hit the ground running, so make sure to detail your experience in building and implementing these processes.
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 don’t miss out on any important updates from us!
How to prepare for a job interview at Valtera Group Ltd
✨Know Your Regulatory Stuff
Make sure you brush up on the latest regulations surrounding ATMPs and autologous stem cell therapies. 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 specific examples from your past roles where you've successfully navigated regulatory challenges or implemented GMP processes. This will help you illustrate your hands-on experience and how it aligns with what the company is looking for.
✨Engage with Stakeholders
Think about how you've previously engaged with stakeholders, especially in a regulatory context. Be ready to discuss your communication strategies and how you’ve built relationships with regulatory bodies like the MHRA.
✨Ask Insightful Questions
Prepare thoughtful questions that show your interest in the company's upcoming projects and challenges. This not only demonstrates your enthusiasm but also gives you a chance to assess if the role is the right fit for you.