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- Tasks: Lead regulatory activities and ensure compliance for clinical and commercial processes.
- Company: A well-established client expanding their quality team across the UK.
- Benefits: Competitive salary, minimal travel, and opportunities for professional growth.
- Other info: Work closely with manufacturing facilities and enjoy a flexible work arrangement.
- Why this job: Be a key player in shaping regulatory strategies in a dynamic environment.
- Qualifications: 5+ years of regulatory experience in pharmaceuticals, especially sterile/biological products.
The predicted salary is between 50000 - 65000 £ per year.
We are supporting a long-standing client with further expansion of their quality team across the UK. This new position will take a business lead for all regulatory activities to support both clinical and commercial processes. You will work closely with several manufacturing facilities across the UK and will be the internal SME on all things regulatory. Due to an increasing and evolving product portfolio, this new function will take a direct responsibility in liaising with the regulatory bodies and work with corporate QA. The split of the role will be around 70% regulatory focused but 30% of your time will still be attributed towards quality activities. Whilst there are several sites, travel will be minimal. However, given the growing nature of the business, there is an expectation for this role to be site based initially with some flexibility moving forwards.
Key experience:
- Established regulatory experience (minimum 5 years) within pharmaceutical sterile/biological products
- IMP experience is essential
- Track record in leading communication with regulatory bodies
- Exceptional stakeholder management skills
- Ability to work in an evolving and fast-paced business
Regulatory Manager in Newcastle upon Tyne employer: RBW Consulting
Contact Detail:
RBW Consulting Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Manager in Newcastle upon Tyne
✨Tip Number 1
Network like a pro! Reach out to your connections in the regulatory and quality sectors. Attend industry events or webinars where you can meet potential employers and showcase your expertise.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of regulatory bodies and current trends in the pharmaceutical industry. We want you to be the go-to person for all things regulatory, so show them you know your stuff!
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you email to express your appreciation and reiterate your interest in the role. It keeps you fresh in their minds.
✨Tip Number 4
Apply through our website! We’ve got loads of opportunities that might just be the perfect fit for you. Plus, it’s a great way to ensure your application gets seen by the right people.
We think you need these skills to ace Regulatory Manager in Newcastle upon Tyne
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Regulatory Manager role. Highlight your established regulatory experience and any specific projects related to pharmaceutical sterile or biological products. 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. Mention your track record in leading communication with regulatory bodies and your exceptional stakeholder management skills. Let us know what makes you tick!
Showcase Relevant Experience: When filling out your application, be sure to showcase your relevant experience, especially your IMP experience. We’re looking for someone who can hit the ground running, so don’t hold back on sharing your achievements in regulatory activities.
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It helps us keep everything organised and ensures your application gets the attention it deserves. Plus, it’s super easy to do!
How to prepare for a job interview at RBW Consulting
✨Know Your Regulatory Stuff
Make sure you brush up on your knowledge of regulatory frameworks, especially those related to pharmaceutical sterile and biological products. Be ready to discuss your experience with IMP submissions and how you've successfully navigated communication with regulatory bodies like the MHRA.
✨Showcase Your Stakeholder Skills
Prepare examples that highlight your exceptional stakeholder management skills. Think about times when you’ve effectively collaborated with different teams or departments, and be ready to explain how you can bring that experience to the new role.
✨Embrace the Fast-Paced Environment
This role is in a rapidly evolving business, so be prepared to discuss how you thrive in fast-paced settings. Share specific instances where you adapted quickly to changes or challenges in your previous roles, particularly in regulatory or quality contexts.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask questions that show your interest in the company’s growth and regulatory strategies. Inquire about their current challenges in regulatory affairs or how they foresee the evolution of their product portfolio impacting the quality team.