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- Tasks: Lead regulatory strategies and ensure compliance for innovative medicinal products.
- Company: Pioneering leader in the biopharmaceutical industry with a focus on innovation.
- Benefits: Remote work flexibility, competitive salary, and opportunities for professional growth.
- Why this job: Make a real impact on healthcare solutions and shape the future of medicines.
- Qualifications: 8+ years in regulatory affairs and strong leadership skills required.
- Other info: Join a diverse team committed to inclusivity and strategic initiatives.
The predicted salary is between 36000 - 60000 £ per year.
Join a pioneering leader in the biopharmaceutical industry as a Senior Manager of Regulatory Affairs, where your expertise will directly impact the development and delivery of innovative medicinal products worldwide. In this strategic role, you will lead regional regulatory strategies, oversee critical agency interactions, and ensure compliance across multiple product portfolios. Your contributions will be vital to maintaining timely approvals, supporting clinical trials, and shaping the future of healthcare solutions.
What You’ll Bring
- Extensive knowledge of regional legislation, regulations, and policies related to medicinal products
- Proven experience in developing and executing regulatory strategies for clinical trial and marketing applications
- Strong track record of managing regulatory submissions and negotiations with health authorities
- Exceptional leadership skills with the ability to guide and collaborate across cross-functional teams
- Excellent communication capabilities, adept at translating complex regulatory information into actionable insights
- Analytical mindset with the ability to assess regulatory risks and develop contingency plans
Nice To Have Skills
- Experience managing or supervising regional regulatory teams or support staff
- Familiarity with expedited pathways such as orphan drug, accelerated approval, and compassionate use programs
- Knowledge of industry best practices in labelling, regulatory documentation, and agency negotiations
- Multilingual proficiency and cultural sensitivity for international collaboration
Preferred Education And Experience
- Bachelor’s degree in Life Sciences, Pharmacy, or a related field; advanced degrees (e.g., Master’s or PhD) are advantageous
- A minimum of 8+ years of regulatory affairs experience within the biopharmaceutical or healthcare industry
- Prior involvement in product development phases from clinical trials through to commercialisation
Other Requirements
- Ability to work primarily remotely with occasional on-site presence in Uxbridge (approximately one day per month)
- Flexibility to support a 12-month contract with an immediate start preferred
- Willingness to stay abreast of evolving global and regional regulatory landscapes and contribute to strategic initiatives
If you are a strategic thinker with a passion for advancing healthcare through effective regulatory leadership, we invite you to bring your expertise to this dynamic role. Take this opportunity to make a meaningful impact—apply now and help shape the future of life-changing medicines.
The Planet Group of Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Senior Manager Regulatory Affairs in Uxbridge employer: Planet Pharma
Contact Detail:
Planet Pharma Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Manager Regulatory Affairs in Uxbridge
✨Tip Number 1
Network like a pro! Reach out to industry contacts on LinkedIn or attend relevant events. We all know that sometimes it’s not just what you know, but who you know that can help you land that Senior Manager role.
✨Tip Number 2
Prepare for interviews by brushing up on your regulatory knowledge and recent industry trends. We recommend practising common interview questions and having examples ready that showcase your leadership skills and strategic thinking.
✨Tip Number 3
Don’t forget to follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. We suggest mentioning something specific from the conversation to show your genuine interest.
✨Tip Number 4
Apply through our website for the best chance at landing the job! We make it easy for you to showcase your skills and experience directly to the hiring team. Don’t miss out on this opportunity!
We think you need these skills to ace Senior Manager Regulatory Affairs in Uxbridge
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the specific skills and experiences mentioned in the job description. Highlight your regulatory affairs expertise and any relevant achievements that align with the role.
Craft a Compelling Cover Letter: Use your cover letter to tell us why you're the perfect fit for this Senior Manager role. Share your passion for regulatory affairs and how your background can help shape the future of healthcare solutions.
Showcase Your Leadership Skills: Since this role requires exceptional leadership, be sure to include examples of how you've successfully guided teams or projects in the past. We want to see your collaborative spirit shine through!
Apply Through Our Website: For the best chance of success, make sure to apply directly through our website. This way, we can easily track your application and get back to you as soon as possible!
How to prepare for a job interview at Planet Pharma
✨Know Your Regulations
Make sure you brush up on the latest regional legislation and regulations related to medicinal products. Being able to discuss specific laws and how they impact regulatory strategies will show your expertise and readiness for the role.
✨Showcase Your Leadership Skills
Prepare examples of how you've successfully led cross-functional teams in the past. Highlight your ability to guide others through complex regulatory processes, as this is crucial for a Senior Manager position.
✨Communicate Clearly
Practice translating complex regulatory information into simple, actionable insights. During the interview, aim to demonstrate your excellent communication skills by explaining how you would approach regulatory submissions and negotiations.
✨Be Ready for Scenario Questions
Expect questions that assess your analytical mindset and risk assessment abilities. Prepare to discuss how you would handle potential regulatory challenges or develop contingency plans for various scenarios in the biopharmaceutical landscape.
