At a Glance
- Tasks: Lead regulatory efforts for innovative medical technology products in a global biotech environment.
- Company: Ground-breaking global biotechnology company focused on ethical innovation.
- Benefits: 25 days annual leave, pension plan, flexible time off, and private medical insurance.
- Other info: Hybrid working model with excellent career growth opportunities.
- Why this job: Join a supportive team and make a real impact in the life sciences sector.
- Qualifications: Experience in regulatory settings with strong analytical and interpersonal skills.
The predicted salary is between 70000 - 90000 £ per year.
A regional lead Regulatory role in a global biotech.
European Regulatory Lead - London or Cambridge with hybrid working.
If you're looking for an opportunity to work as part of a global team and utilise a breadth of European regulatory capability in a region-lead role, this could be an excellent opportunity for you with a ground-breaking global biotechnology company with a focus on ethical innovation.
Potentially suited to either an experienced in-house practitioner or someone looking for their first role from practice, either individual would find substantial support across an experienced team both locally and throughout the business' global hubs.
Role:- Focusing primarily on regulatory and quality matters of medical technology products, including RUO and clinical offerings.
- Advise the business and its teams/functions globally (EMEALA) on complex regulatory frameworks.
- Working closely with teams across Reg Affairs, Med Affairs, Marketing, Compliance and Commercial among others.
- Supporting regional submissions, market-access strategies and post-market matters.
- Evaluating and providing cross-function guidance on regulating changes and industry adaptations.
- UK or dual UK/EU Qualified.
- Senior advisory and commercial experience in a regulatory setting, ideally in an international setting.
- Demonstrable life sciences and medical devices regulatory knowledge/experience.
- An essential skill will be providing practical solutions from analytical judgement of regulatory risk and/or change.
- Multilingual skills an advantage, but not essential.
- Pragmatic and commercially focused with excellent interpersonal skills.
- 25 days annual leave plus bank holidays.
- Pension plan.
- Flexible time off.
- Bonus scheme.
- Private Medical Insurance.
- Life Assurance.
- On-site gym.
For further information and a confidential discussion, please contact sean.dodsworth@erringtonlegal.co.uk.
We are an equal opportunities recruiter, committed to ensuring an inclusive and supportive recruitment process. We embrace and promote diversity as we understand the importance and value of this both for us and our clients.
Locations
Associate Director - Regulatory in Cambridge, London employer: Errington Legal
Join a pioneering global biotechnology company that champions ethical innovation and offers a dynamic work environment in London or Cambridge. With a strong emphasis on employee growth, you will benefit from a supportive team culture, flexible working arrangements, and a comprehensive benefits package including private medical insurance and a bonus scheme. This role not only provides the opportunity to lead in regulatory affairs but also fosters collaboration across diverse teams, making it an ideal place for professionals seeking meaningful and rewarding employment.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Director - Regulatory in Cambridge, London
✨Tip Number 1
Network like a pro! Reach out to your connections in the biotech and regulatory fields. Attend industry events or webinars to meet potential employers and get your name out there. Remember, it’s all about who you know!
✨Tip Number 2
Prepare for interviews by researching the company and its regulatory challenges. Tailor your answers to show how your experience aligns with their needs. We want to see you shine, so practice common interview questions and have your own ready!
✨Tip Number 3
Follow up after interviews! A quick thank-you email can set you apart from other candidates. It shows your enthusiasm for the role and keeps you fresh in their minds. Plus, it’s just good manners!
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of opportunities that might be perfect for you. Keep an eye on our listings and make sure your application stands out by highlighting your relevant skills and experiences.
We think you need these skills to ace Associate Director - Regulatory in Cambridge, London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the specific skills and experiences that match the Associate Director - Regulatory role. Highlight your regulatory knowledge and any relevant experience in life sciences or medical devices to catch our eye!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about this role and how your background makes you a perfect fit. Don’t forget to mention your experience with regulatory frameworks and your ability to provide practical solutions.
Showcase Your Team Spirit:Since this role involves working closely with various teams, make sure to highlight your interpersonal skills and any collaborative projects you've been part of. We love seeing candidates who can work well in a global team environment!
Apply Through Our Website:We encourage you to apply directly through our website for the best chance of getting noticed. It’s the easiest way for us to keep track of your application and ensure it reaches the right people!
How to prepare for a job interview at Errington Legal
✨Know Your Regulatory Stuff
Make sure you brush up on your knowledge of European regulatory frameworks, especially those related to medical technology products. Be ready to discuss specific examples from your experience that demonstrate your understanding and how you've navigated complex regulations.
✨Showcase Your Interpersonal Skills
This role requires excellent communication and collaboration with various teams. Prepare to share instances where you've successfully worked with cross-functional teams, highlighting your ability to provide practical solutions and guidance on regulatory matters.
✨Be Ready for Scenario Questions
Expect questions that ask how you would handle specific regulatory challenges or changes in the industry. Think through potential scenarios beforehand and formulate your responses, focusing on your analytical judgement and risk assessment skills.
✨Ask Insightful Questions
At the end of the interview, have a few thoughtful questions prepared about the company's approach to regulatory challenges or their team dynamics. This shows your genuine interest in the role and helps you assess if it's the right fit for you.
