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- Tasks: Lead a team in managing regulatory documentation and public reporting for pharmaceuticals.
- Company: Join a respected regulatory organisation making a significant impact in the pharmaceutical sector.
- Benefits: Enjoy a hybrid work model, competitive salary, and the chance to influence public transparency.
- Why this job: This role offers a unique opportunity to shape regulatory standards and drive meaningful change.
- Qualifications: Bachelor's degree in a scientific discipline and strong leadership experience required.
- Other info: 6-month contract with a full-time commitment of 37 hours per week.
The predicted salary is between 26700 - 44600 £ per year.
Weybridge, Surrey (Hybrid – three-days onsite, following initial training) 6-month contract | circa £44,500 pro rata | Full-time (37 hours/week)
We’re working with a respected regulatory organisation that needs an experienced scientific professional to step in for a 6-month assignment as a Regulatory Compliance Lead (Documentation and Reporting). In this role, you’ll lead a small team overseeing the documentation, approvals and public reporting relating to pharmaceuticals – ensuring authorisations are correctly processed, supply issues are addressed early and regulatory expertise in a leadership role that makes a strong impact. You’ll be driving improvements on how supply operations are delivered and communicated.
What you’ll be doing:
- Leading and line-managing a small team of specialists
- Overseeing the assessment of complex or unusual regulatory applications
- Managing the production and review of public assessment reports and product information
- Coordinating responses to supply issues and shortages
- Engaging with stakeholders to ensure early intelligence on supply challenges
- Leading key regulatory meetings and contributing to discussions
- Driving process improvements and ensuring compliance with regulatory and quality standards
What we’re looking for:
- A bachelor’s degree or higher in a relevant scientific discipline (such as life sciences, biological sciences, or related fields)
- Strong leadership experience with an ability to guide teams through complex regulatory work
- Excellent communicator, confident presenting technical and regulatory information clearly
- Familiarity with authorisation procedures, regulatory standards, and SOPs (or ability to rapidly learn)
- Highly organised, able to prioritise conflicting demands and meet tight deadlines
Why apply? This is a rare opportunity to step into a regulatory leadership role that directly impacts the UK — shaping documentation standards, improving public transparency, and driving meaningful outcomes.
Interested in learning more? Apply today – we’re shortlisting now.
Regulatory Compliance Lead (Documentation & Reporting) employer: Amber Employment Services
Contact Detail:
Amber Employment Services Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Compliance Lead (Documentation & Reporting)
✨Tip Number 1
Familiarise yourself with the latest regulatory standards and authorisation procedures relevant to pharmaceuticals. This knowledge will not only help you in interviews but also demonstrate your commitment to staying updated in a fast-paced environment.
✨Tip Number 2
Highlight your leadership experience by preparing specific examples of how you've successfully guided teams through complex regulatory challenges. Be ready to discuss these scenarios during your conversations with us.
✨Tip Number 3
Practice articulating technical and regulatory information clearly and confidently. You may be asked to present or explain complex concepts, so honing this skill will set you apart from other candidates.
✨Tip Number 4
Network with professionals in the regulatory field, especially those who have experience in documentation and reporting. Engaging with industry peers can provide valuable insights and potentially lead to referrals for the role.
We think you need these skills to ace Regulatory Compliance Lead (Documentation & Reporting)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in regulatory compliance and leadership. Use specific examples that demonstrate your ability to manage teams and handle complex regulatory applications.
Craft a Compelling Cover Letter: Write a cover letter that clearly outlines your motivation for applying and how your background aligns with the job requirements. Emphasise your communication skills and experience in driving process improvements.
Highlight Relevant Qualifications: In your application, be sure to mention your educational background in life sciences or related fields. If you have familiarity with authorisation procedures and regulatory standards, make that clear as well.
Showcase Leadership Experience: Provide examples of your leadership experience in your application. Discuss how you've successfully guided teams through complex projects and how you’ve contributed to improving compliance and quality standards.
How to prepare for a job interview at Amber Employment Services
✨Showcase Your Leadership Skills
As a Regulatory Compliance Lead, you'll be managing a team. Be prepared to discuss your leadership style and provide examples of how you've successfully guided teams through complex regulatory challenges in the past.
✨Demonstrate Your Regulatory Knowledge
Familiarise yourself with the latest regulatory standards and authorisation procedures relevant to pharmaceuticals. Be ready to discuss how you can apply this knowledge to improve documentation and reporting processes.
✨Prepare for Technical Questions
Expect questions that assess your understanding of compliance and quality standards. Brush up on key concepts and be ready to explain how you would handle specific regulatory scenarios or challenges.
✨Engage with Stakeholders
Since stakeholder engagement is crucial in this role, think of examples where you've effectively communicated with various parties. Highlight your ability to gather intelligence on supply issues and how you’ve addressed them in the past.
