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- Tasks: Join us as a Regulatory Affairs Consultant, shaping compliance strategies and managing regulatory submissions.
- Company: PE Global is a dynamic consultancy focused on personal care, offering exciting opportunities in the FMCG sector.
- Benefits: Enjoy hybrid working, competitive pay, and the chance to transition into a permanent role.
- Why this job: Be part of a collaborative team, influence regulatory practices, and make a real impact in the industry.
- Qualifications: A Bachelor's degree in Life Sciences, Chemistry, or Pharmacy, plus 5-8 years in Regulatory Affairs is essential.
- Other info: This role requires full right to work in the UK; no sponsorship available.
The predicted salary is between 52000 - 78000 £ per year.
Job Description
PE Global is hiring a Regulatory Affairs Consultant (FMCG/EMEA) for our personal care client based in High Wycombe office until Dec and Reading Office thereafter from January. The rate for this role is £67.00 Umbrella p/hour.
- Initial 6 month role but with the opportunity to apply for a perm role
- Hybrid working, onsite at least 2 days per week.
Responsibilities:
Regulatory Strategy & Execution
- Develop and implement global and/or regional regulatory strategies in collaboration with internal stakeholders.
- Prepare and submit regulatory dossiers and documentation aligned with applicable regulations.
- Support regulatory activities for EU procedures (e.g., MRP, DCP, national).
- Monitor the progress of applications and proactively manage regulatory timelines and risks.
- Stay abreast of evolving regional regulatory requirements and ensure knowledge is applied effectively.
Regulatory Compliance
- Ensure regulatory systems and documentation are current and compliant.
- Participate in SOP training, audits, and inspections alongside the Quality function.
- Document and track communications and outcomes with regulatory authorities.
- Identify, escalate, and support resolution of compliance issues, implementing corrective/preventive actions as needed.
Cross-Functional Collaboration
- Represent Regulatory Affairs in cross-functional teams, providing expert guidance.
- Support business continuity and crisis management initiatives through effective regulatory leadership.
- Maintain strong relationships with internal and external stakeholders using clear and persuasive communication.
Essential Qualifications & Experience
- Bachelor's Degree (or higher) in Life Sciences, Chemistry, or Pharmacy.
- Proven experience in Regulatory Affairs across medicines and food supplements within the EMEA region.
- Deep understanding of EMEA regulatory frameworks and product lifecycle management.
- Proficiency in English (verbal and written).
- Ideally 5-8 years experience.
PE Global cannot provide sponsorship. Candidates will need the full right to live and work full time within the UK for at least the next 12 months.
Regulatory Affairs Consultant employer: PE Global
Contact Detail:
PE Global Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Consultant
✨Tip Number 1
Network with professionals in the Regulatory Affairs field, especially those who have experience in FMCG and EMEA regulations. Attend industry events or webinars to connect with potential colleagues and learn about the latest trends.
✨Tip Number 2
Familiarise yourself with the specific regulatory frameworks relevant to personal care products in the EMEA region. This knowledge will not only boost your confidence but also demonstrate your commitment to the role during interviews.
✨Tip Number 3
Prepare to discuss your previous experiences in regulatory strategy and compliance. Be ready to provide examples of how you've successfully managed regulatory timelines and resolved compliance issues in past roles.
✨Tip Number 4
Showcase your communication skills by practising how you would explain complex regulatory concepts to non-experts. This is crucial for cross-functional collaboration and will set you apart as a candidate who can bridge gaps between teams.
We think you need these skills to ace Regulatory Affairs Consultant
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in Regulatory Affairs, particularly within the FMCG sector and EMEA region. Use keywords from the job description to demonstrate your fit for the role.
Craft a Compelling Cover Letter: Write a cover letter that outlines your understanding of regulatory strategies and compliance. Mention specific examples of how you've successfully managed regulatory timelines and collaborated with cross-functional teams.
Highlight Relevant Qualifications: Clearly state your educational background and any certifications related to Life Sciences, Chemistry, or Pharmacy. Emphasise your years of experience in Regulatory Affairs and your proficiency in English.
Showcase Communication Skills: In your application, provide examples of how you've effectively communicated with regulatory authorities and internal stakeholders. This is crucial for the role, so make it stand out.
How to prepare for a job interview at PE Global
✨Know Your Regulatory Frameworks
Make sure you have a solid understanding of the EMEA regulatory frameworks relevant to the role. Brush up on recent changes and how they impact product lifecycle management, as this will show your commitment and expertise during the interview.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Think about past experiences where you successfully navigated regulatory challenges and be ready to discuss the strategies you employed.
✨Highlight Cross-Functional Collaboration
Since the role involves working with various teams, prepare examples that demonstrate your ability to collaborate effectively. Discuss how you've built relationships and communicated regulatory requirements to non-regulatory stakeholders.
✨Showcase Your Communication Skills
Effective communication is key in Regulatory Affairs. Be prepared to articulate complex regulatory concepts clearly and persuasively. Practise explaining your past projects or regulatory submissions in a way that anyone can understand.
