Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead regulatory strategies for life-changing medicines and ensure compliance across global markets.
- Company: Join a growing global team at a leading pharmaceutical company.
- Benefits: Competitive salary, career growth, and the chance to make a real impact.
- Why this job: Help bring safe, effective medicines to patients worldwide while advancing your career.
- Qualifications: Experience in Regulatory Affairs, especially with Biologics or Vaccines, is essential.
- Other info: Dynamic work environment with opportunities in Barcelona, Belfast, London, and Mumbai.
The predicted salary is between 55000 - 70000 £ per year.
G&L have multiple positions available for Regulatory Affairs Manager. We are growing our teams on a global basis; there has never been a more exciting time to join us!
Please note that we have vacancies in Barcelona, Belfast, London and Mumbai. If you have the experience we require and can work in one of our offices, we want to hear from you!
Do you want to help bring life-changing medicines to the world? Are you passionate about science, strategy, and regulatory excellence? As a CMC Regulatory Manager, you’ll play a key role in ensuring that high-quality medicines continue to reach patients safely and efficiently across global markets.
You’ll sit at the intersection of science, manufacturing, and regulatory strategy, guiding post-approval activities and ensuring that every change to our products meets global regulatory standards. If you enjoy solving complex problems, working across teams, and translating technical data into clear regulatory strategies, this role is for you.
What You’ll Be Doing
- Lead Post-Approval Regulatory Strategies
Develop and implement regulatory strategies for post-approval CMC activities, including: Variations, Renewals, Market expansions, Annual reports. Your work ensures our products continue to meet global regulatory expectations throughout their lifecycle. - Evaluate Manufacturing and Quality Changes
Review change controls and assess how manufacturing or quality updates impact regulatory filings. You’ll determine: Regulatory classification of changes, Submission requirements, Global regulatory impact. - Review Critical Scientific Data
Collaborate with quality and manufacturing teams to review key reports such as: Process validation studies, Stability studies, Analytical method validation. You’ll ensure all data supports regulatory submissions and meets compliance standards. - Collaborate Across Teams
Work closely with colleagues across: Manufacturing, Supply Chain, Quality Control, Quality Assurance, Global Regulatory teams. Your coordination keeps submissions accurate, complete, and on schedule. - Shape Regulatory Submissions
Draft and review CMC sections of regulatory documents, including: Variation submissions, Responses to health authority questions, Technical regulatory documentation. Your expertise helps transform complex scientific information into clear regulatory narratives. - Manage Regulatory Systems
Oversee projects within Regulatory Information Management (RIM) systems, ensuring global submissions are tracked, maintained, and compliant. - Anticipate and Manage Risk
Identify potential regulatory challenges early and implement strategies to keep projects on track.
What You Bring
- Experience
Experience in Regulatory Affairs within the pharmaceutical industry, Strong background in CMC or technical regulatory documentation, Experience preparing CMC sections of regulatory submissions or variations, Experience in validation, quality assurance, or pharmaceutical production is highly valued. - Technical Knowledge
Strong understanding of CMC and post-approval regulatory requirements, Knowledge of: Stability studies, Process validation, Analytical method validation, Comparability studies, Experience working with Biological products or vaccines is a mandatory requirement for this role. - Skills That Make You Shine
Exceptional attention to detail, Strong problem-solving ability, Excellent project management skills, Ability to collaborate with cross-functional global teams. - Languages
Fluency in English (written and spoken), Additional language (French, Italian, or German) is a plus.
Why This Role Matters
Your work ensures that safe, effective medicines continue to reach patients around the world — even as products evolve and improve. In short: you help science move forward, compliantly.
Please only apply for this role if you have demonstrable experience working with Biologics or Vaccines.
Regulatory Affairs Manager in City of London employer: G&L Scientific
Contact Detail:
G&L Scientific Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Manager in City of London
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those already working at G&L. A friendly chat can open doors and give you insider info that could make your application stand out.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of CMC and regulatory strategies. We want to see your passion for bringing life-changing medicines to the world, so be ready to discuss how your experience aligns with their needs.
✨Tip Number 3
Showcase your problem-solving skills! Think of examples from your past work where you tackled complex regulatory challenges. This will demonstrate your ability to navigate the tricky waters of regulatory affairs.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re serious about joining the team at G&L.
We think you need these skills to ace Regulatory Affairs Manager in City of London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Regulatory Affairs Manager role. Highlight your experience in CMC and any relevant projects you've worked on. 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 of bringing life-changing medicines to the world. Keep it engaging and personal!
Showcase Your Problem-Solving Skills: In your application, don’t forget to mention specific examples where you've tackled complex regulatory challenges. We love seeing how you approach problems and find solutions, especially in a cross-functional team setting.
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 shows you’re keen on joining our team!
How to prepare for a job interview at G&L Scientific
✨Know Your Regulatory Stuff
Make sure you brush up on your knowledge of CMC and post-approval regulatory requirements. Be ready to discuss specific examples from your experience, especially related to biologics or vaccines, as this will show that you understand the complexities of the role.
✨Showcase Your Problem-Solving Skills
Prepare to share instances where you've tackled complex regulatory challenges. Think about how you identified potential issues and what strategies you implemented to keep projects on track. This will demonstrate your proactive approach and critical thinking.
✨Collaboration is Key
Since the role involves working with various teams, be ready to talk about your experience collaborating across departments. Highlight any successful projects where teamwork was essential, and how you ensured submissions were accurate and timely.
✨Be Detail-Oriented
Attention to detail is crucial in regulatory affairs. During the interview, mention how you ensure compliance and accuracy in your work. You could even bring examples of documents you've drafted or reviewed to illustrate your meticulous nature.