At a Glance
- Tasks: Lead regulatory strategy and ensure successful outcomes for pharmaceutical products across Europe.
- Company: Leading pharmaceutical company with a focus on innovation and collaboration.
- Benefits: Competitive hourly rate, hybrid work model, and opportunity to shape industry standards.
- Other info: Flexible working hours with a dynamic and supportive team environment.
- Why this job: Make a real impact in the pharmaceutical industry while working with global teams.
- Qualifications: Degree in life sciences and strong experience in European Regulatory Affairs required.
The predicted salary is between 56000 - 68000 £ per year.
Do you have the right skills and experience for this role? Read on to find out and make your application.
Location: Maidenhead/Remote (hybrid)
Duration: 12 months initial (four days per week / 0.8 FTE)
Rate: £70-85 per hour (based on experience)
We are working with a leading pharmaceutical company who are seeking an experienced Senior Manager, Regulatory Affairs to shape and drive regulatory strategy across the Europe Area. This high-impact role will work across development and marketed products, partnering closely with global teams, affiliates and health authorities to ensure successful regulatory outcomes.
Key Responsibilities- Lead the development and implementation of regulatory strategies and risk assessments for assigned products across the Europe Area
- Represent regional regulatory requirements within global regulatory project teams to ensure appropriate consideration in global strategy
- Collaborate with affiliate Regulatory Affairs teams to guide submissions, health authority interactions and life-cycle management activities
- Assess scientific data for regulatory submissions, identify gaps, and develop mitigation strategies to support approvals
- Monitor evolving European legislation and lead the development of regulatory responses and policy implementation
- Degree in pharmacy, biology, chemistry, pharmacology, or related life sciences discipline
- Strong experience in European Regulatory Affairs, including centralised, MRP/DCP and national procedures
- Proven track record leading regulatory activities for development products (e.g., scientific advice, PIP)
- Effective communicator able to work across complex international and matrixed environments
- Strong leadership, organisational skills and ability to work independently with minimal supervision
Senior) Manager, Regulatory Affairs in Maidenhead employer: Carbon
Join a leading pharmaceutical company that values innovation and collaboration, offering a dynamic work culture where your expertise in Regulatory Affairs will directly impact the success of products across Europe. With a hybrid working model based in Maidenhead, you will enjoy flexibility while being part of a team that prioritises professional growth and development, ensuring you have the resources and support to excel in your role. This is an exceptional opportunity to contribute to meaningful projects in a supportive environment that champions regulatory excellence.
StudySmarter Expert Advice🤫
We think this is how you could land Senior) Manager, Regulatory Affairs in Maidenhead
✨Tip Number 1
Network like a pro! Reach out to your connections in the regulatory affairs field, especially those who have experience with European regulations. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of current European legislation and regulatory strategies. We recommend having specific examples ready that showcase your leadership and problem-solving skills in past roles.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, send 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 for the best chance at landing that Senior Manager role! We’re always on the lookout for top talent, and applying directly helps us see your application first.
We think you need these skills to ace Senior) Manager, Regulatory Affairs in Maidenhead
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your experience in European Regulatory Affairs. We want to see how your background aligns with the key responsibilities mentioned in the job description, so don’t hold back on showcasing your relevant 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 the Senior Manager role. We love seeing candidates who can articulate their passion for regulatory affairs and how they can contribute to our team.
Showcase Your Leadership Skills:Since this role requires strong leadership, make sure to include examples of how you've led teams or projects in the past. We’re looking for someone who can drive regulatory strategy, so let us know how you’ve done that before!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it makes the process smoother for everyone involved!
How to prepare for a job interview at Carbon
✨Know Your Regulatory Stuff
Make sure you brush up on your knowledge of European regulatory affairs, especially centralised and MRP/DCP procedures. Be ready to discuss specific examples from your past experiences where you successfully led regulatory activities or navigated complex submissions.
✨Showcase Your Leadership Skills
This role requires strong leadership, so think of instances where you've led a team or project. Prepare to share how you motivated others, managed conflicts, and drove successful outcomes in a matrixed environment.
✨Understand the Company’s Products
Research the pharmaceutical company and their products thoroughly. Familiarise yourself with their portfolio and any recent news or developments. This will help you tailor your responses and demonstrate your genuine interest in the role.
✨Prepare for Scenario Questions
Expect questions that assess your problem-solving skills and ability to handle regulatory challenges. Think about potential scenarios you might face in this role and how you would approach them, particularly regarding risk assessments and policy implementation.
