At a Glance
- Tasks: Lead regulatory strategies and submissions for innovative medicines in the UK.
- Company: Join a global biopharmaceutical leader focused on breakthrough therapies.
- Benefits: Competitive salary, career development, and a supportive team environment.
- Other info: Exciting opportunity for growth in a collaborative and innovative setting.
- Why this job: Make a real impact on patient care while managing a dynamic team.
- Qualifications: Degree in Life Sciences and significant UK regulatory experience required.
The predicted salary is between 60000 - 75000 £ per year.
Apsida Life Science are currently partnering with a global biopharmaceutical company recognised for developing innovative medicines that address complex and serious diseases. The organisation combines strong scientific expertise with a patient-first approach, focusing on improving standards of care through breakthrough therapies and close collaboration with healthcare systems. They are seeking a Senior Regulatory Affairs Manager to support their UK portfolio and be responsible for managing a small team.
Location: M4 Corridor
Responsibilities:
- Acts as the primary Regulatory contact for identified therapeutic area.
- Develop regulatory strategies and timely submissions to the MHRA, as well as developing and maintaining a strong relationship with MHRA/local pharma trade associations.
- Act as Regulatory liaison with Area and local UK cross functional teams to ensure UK strategies align with global strategies, whilst maintaining compliance with local regulations.
- Ensure compliance with UK legislation for medicines, clinical trials and PIPs.
- Responsible for line managing a small team.
Requirements:
- Degree in Life Sciences or a related field.
- Significant experience within UK regulatory processes and MHRA interactions.
- Must have proven, recent line management experience.
- Experience managing regulatory submissions and lifecycle activities.
- Highly developed people skills and a positive, can-do attitude.
If you are interested in learning more, please reach out to Geneva Jones at Apsida Life Science: www.apsida.co.uk +44(0)7441341762
Apsida Life Science is a specialist recruitment business based in London (UK), Redhill (UK) & Boston (USA) that is dedicated to delivering the best talent to the Life Science industry. We believe there is a gap in the market for a cost effective, high quality and trusted recruitment service that puts the candidate journey at the heart of the recruitment process.
Senior Manager Regulatory Affairs - MHRA in London employer: Apsida Life Science
Apsida Life Science is an exceptional employer, offering a dynamic work environment in the M4 Corridor that fosters innovation and collaboration within the biopharmaceutical sector. With a strong commitment to employee development, the company provides ample opportunities for growth and advancement, alongside a supportive culture that prioritises a patient-first approach. Joining Apsida means being part of a team that is dedicated to making a meaningful impact on healthcare through groundbreaking therapies and strategic partnerships.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Manager Regulatory Affairs - MHRA in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the regulatory affairs field, especially those who have experience with MHRA. Attend industry events or webinars to make connections and learn more about the latest trends.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of UK regulatory processes. Be ready to discuss your past experiences managing submissions and leading teams, as these will be key topics for the Senior Manager role.
✨Tip Number 3
Showcase your people skills! In your conversations, highlight how you've successfully managed teams and built relationships with stakeholders. A positive attitude goes a long way in making a great impression.
✨Tip Number 4
Don't forget to apply through our website! We’ve got loads of resources to help you land that dream job, and applying directly can give you an edge over other candidates.
We think you need these skills to ace Senior Manager Regulatory Affairs - MHRA in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Senior Manager Regulatory Affairs role. Highlight your experience with MHRA and regulatory submissions, as well as any leadership roles you've held. 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 passionate about regulatory affairs and how you can contribute to our mission. Keep it concise but impactful – we love a good story!
Showcase Your Team Management Skills:Since this role involves line management, be sure to highlight your experience in leading teams. Share examples of how you've motivated and developed your team members. We value strong people skills here at StudySmarter!
Apply Through Our Website:We encourage you to apply directly through our website for a smoother application process. It helps us keep track of your application and ensures you don’t miss out on any updates. Let’s get started on this journey together!
How to prepare for a job interview at Apsida Life Science
✨Know Your Regulatory Stuff
Make sure you brush up on the latest UK regulatory processes and MHRA guidelines. Being able to discuss recent changes or challenges in the regulatory landscape will show that you're not just knowledgeable but also proactive in your field.
✨Showcase Your Leadership Skills
Since this role involves line management, be prepared to share specific examples of how you've successfully led a team. Highlight your people skills and how you've fostered a positive environment, as this will resonate well with the interviewers.
✨Align with Their Patient-First Approach
Understand the company's mission of improving patient care through innovative therapies. Be ready to discuss how your previous experiences align with this ethos and how you can contribute to their goals.
✨Prepare for Scenario Questions
Expect questions that assess your problem-solving abilities in real-world regulatory scenarios. Think of examples where you've navigated complex submissions or compliance issues, and be ready to explain your thought process and outcomes.
