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- Tasks: Join us as a Regulatory Affairs Consultant, managing product labelling and compliance for self-care products.
- Company: Work with a leading Consumer Health organisation focused on innovative self-care solutions.
- Benefits: Enjoy a competitive pay rate of £65ph PAYE and potential for permanent placement.
- Why this job: Be part of a dynamic team driving regulatory strategy in a fast-paced environment.
- Qualifications: Must have a B.S. in Chemistry, Biology, or related fields and relevant regulatory experience.
- Other info: This role requires on-site presence in High Wycombe, UK, twice a week.
Job Description
Job Title: Regulatory Affairs Specialist/Consultant – Self Care
Job Type: 6-monthcontract, likelihood of going permanent (Inside IR35)
Location: High Wycombe, UK – 2x a week in the office
Pay Rate: £65ph PAYE
We are partnered with a leading Consumer Health organization who are looking for an experienced Regulatory Consultant to join on a 6-month contract basis. This role will be dedicated to the self-care (Medicines, food supplements, cosmetics) portfolio.
Responsibilities:
- Regulatory review and approval of product labelling for Medicines, food supplements, cosmetics classes per the company portfolio in mainly UK & EU and EMEA
- Assists in the preparation of dossiers and submission packages for the registration and maintenance of products
- Participate in the development and implementation of, and maintain compliance with, all applicable Processes, SOPs
- Regulatory review and approval and advertising or promotional copy
- Support the Regulatory team with specific tasks per the needs of the department, which may include claims tracker updates, databases, compliance tasks
- Work with the regulatory team to develop project implementation plans and manage resource planning to ensure on time completion of projects and tasks
- Project management and implementation of regulatory changes to company assets (product label and promotional materials)
- Work with cross functional partners to drive regulatory strategy and implementation
- Regulatory review and approval of key documents before product approval
- Complete market impact assessments
Experience/Qualifications:
- Minimum B.S. Chemistry, Biology, or related fields
- Significant experience in Consumer Health/ Personal care Regulatory affairs mainly with new registrations, promotional material and artwork review/approval at all stages of life cycle management, with demonstrated accountability of managing multiple brands.
- Well versed with UK ASA, CAP, BCAP Guidance for Advertising, proven record of successful project management of dossiers with ClearCast
- Strong knowledge and application of the UK & EU
- Excellent leadership, communication, and organizational skills
- Attention to detail, effective in written and oral communication
- Works independently to plan, conduct, and manage regulatory projects to meet department and company objectives
- Responsible for identifying, implementing and managing key RA Departmental projects and/or strategies based on both short- and long-term RA Department objectives.
You must be able to be based on site 2x a week in Buckinghamshire, UK, and have the FULL right to work in the UK. For more information or to apply please reach out to lucy.kirkaldy@cpl.com
Regulatory Affairs Consultant employer: Cpl Life Sciences
Contact Detail:
Cpl Life Sciences 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 consumer health. Attend industry events or webinars to connect with potential colleagues and learn about the latest trends and challenges in the sector.
✨Tip Number 2
Familiarise yourself with the specific regulations and guidelines related to self-care products in the UK and EU. This knowledge will not only boost your confidence but also demonstrate your commitment and expertise during interviews.
✨Tip Number 3
Prepare to discuss your previous experiences managing multiple brands and projects in regulatory affairs. Be ready to provide examples of how you successfully navigated complex regulatory processes and collaborated with cross-functional teams.
✨Tip Number 4
Showcase your attention to detail and organisational skills by preparing a mock project plan or dossier that highlights your approach to regulatory compliance. This can serve as a practical demonstration of your capabilities during the interview process.
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 in consumer health and self-care products. Use keywords from the job description to demonstrate your fit for the role.
Craft a Compelling Cover Letter: Write a cover letter that specifically addresses the responsibilities and qualifications mentioned in the job description. Share examples of your past experiences that align with the requirements, especially your project management skills and knowledge of UK & EU regulations.
Showcase Your Attention to Detail: In your application, emphasise your attention to detail by providing specific examples of how you have successfully managed regulatory projects or reviewed promotional materials. This will help demonstrate your suitability for the role.
Follow Up: After submitting your application, consider sending a polite follow-up email to express your continued interest in the position. This can help keep you on the radar of the hiring team and show your enthusiasm for the role.
How to prepare for a job interview at Cpl Life Sciences
✨Know Your Regulatory Frameworks
Familiarise yourself with the UK and EU regulatory frameworks, especially those related to self-care products. Be prepared to discuss how these regulations impact product labelling and compliance, as this will demonstrate your expertise in the field.
✨Showcase Project Management Skills
Highlight your experience in managing multiple brands and projects simultaneously. Prepare examples of past projects where you successfully implemented regulatory changes or managed submissions, as this will illustrate your ability to handle the responsibilities of the role.
✨Demonstrate Attention to Detail
Since the role requires a keen eye for detail, be ready to discuss specific instances where your attention to detail made a significant difference in your work. This could include examples of successful dossier preparations or compliance tasks you've completed.
✨Prepare for Cross-Functional Collaboration
The job involves working with cross-functional teams, so think of examples where you've effectively collaborated with other departments. Discuss how you communicated regulatory strategies and ensured alignment on project goals, showcasing your teamwork skills.
