At a Glance
- Tasks: Lead regulatory activities and ensure compliance for clinical and commercial processes.
- Company: Join 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 be the go-to expert on regulatory matters.
- Why this job: Make a real impact in a dynamic environment with evolving product portfolios.
- Qualifications: 5+ years of regulatory experience in pharmaceutical sterile/biological products required.
The predicted salary is between 50000 - 70000 € 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 London employer: LinkedIn
As a Regulatory Manager with us, you will join a dynamic and supportive team dedicated to quality and compliance in the pharmaceutical sector. Our company fosters a collaborative work culture that prioritises employee development, offering ample opportunities for growth and advancement within a rapidly expanding organisation. Located across the UK, we provide a flexible working environment that values your expertise while ensuring minimal travel, making it an ideal place for professionals seeking meaningful and rewarding careers.
StudySmarter Expert Advice🤫
We think this is how you could land Regulatory Manager in London
✨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 recent changes in regulations. We want you to be the go-to person for all things regulatory, so show them you’re on top of your game!
✨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 perfect for you. Plus, it’s a great way to ensure your application gets the attention it deserves.
We think you need these skills to ace Regulatory Manager in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to highlight your regulatory experience, especially in pharmaceutical sterile/biological products. We want to see how your skills align with the job description, so don’t be shy about showcasing your IMP experience and stakeholder management skills!
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. We love seeing candidates who can articulate their passion for regulatory affairs and quality management, so let your personality come through while keeping it professional.
Showcase Relevant Achievements:When filling out your application, don’t forget to include specific achievements that demonstrate your expertise in liaising with regulatory bodies. We’re looking for concrete examples of how you’ve successfully navigated regulatory challenges in the past.
Apply Through Our Website:We encourage you to apply directly through our website for a smoother process. It helps us keep track of your application and ensures you don’t miss any important updates. Plus, it’s super easy – just follow the prompts and you’ll be set!
How to prepare for a job interview at LinkedIn
✨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 prepared to discuss your experience with IMP submissions and how you've successfully navigated communication with regulatory bodies in the past.
✨Showcase Your Stakeholder Management Skills
This role requires exceptional stakeholder management skills, so think of examples where you've effectively collaborated with different teams or departments. Be ready to explain how you’ve built relationships and managed expectations with both internal and external stakeholders.
✨Demonstrate Adaptability
Given the fast-paced nature of the business, it’s crucial to show that you can adapt to changing circumstances. Prepare to share instances where you’ve successfully managed evolving priorities or tackled unexpected challenges in your previous roles.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask questions that show your interest in the company and the role. Inquire about their current product portfolio, future regulatory challenges they foresee, or how the quality team collaborates across sites. This not only shows your enthusiasm but also helps you gauge if the company is the right fit for you.
