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For Companies At a Glance
- Tasks: Ensure compliance of chemical products with global regulations and manage regulatory documentation.
- Company: Join a dynamic team focused on innovative chemical solutions for cosmetics, pharmaceuticals, and home care.
- Benefits: Enjoy flexible working options, professional development opportunities, and a collaborative work environment.
- Why this job: Be part of a mission-driven company that values compliance and innovation in the chemical industry.
- Qualifications: Bachelor’s degree in a relevant field and 2–5 years of regulatory experience required.
- Other info: Opportunity to work with cross-functional teams and make a real impact on product compliance.
The predicted salary is between 36000 - 60000 £ per year.
Job Description
Our clients are seeking a proactive and detail-oriented Regulatory Affairs Specialist to join their growing team. You will play a critical role in ensuring that our chemical products meet all applicable regulatory requirements across the cosmetics, pharmaceutical, and home care sectors. This position requires an understanding of global chemical regulations and experience coordinating with cross-functional teams to support product compliance from development to market launch.
Key Responsibilities:
- Ensure compliance of raw materials and finished products with relevant chemical regulations (e.g., REACH, CLP, FDA, EU Cosmetics Regulation, EPA, etc.).
- Prepare, review, and maintain regulatory documentation including safety data sheets (SDS), product dossiers, technical files, and product registrations.
- Serve as the regulatory point of contact for internal teams (R&D, Marketing, QA, Sales) and external regulatory bodies or clients.
- Monitor changes in global regulations and provide impact assessments and guidance to the business.
- Coordinate regulatory submissions for product approvals, renewals, and amendments in various markets.
- Manage ingredient listings and restrictions based on applicable legislations (e.g., INCI for cosmetics, pharmacopeias for pharmaceuticals).
- Support product labeling and claims compliance across all relevant product lines.
- Participate in audits and inspections, ensuring readiness and full documentation availability.
- Contribute to continuous improvement in regulatory processes and tools.
Qualifications & Skills:
- Bachelor’s degree in Chemistry, Regulatory Affairs, Pharmaceutical Sciences, or a related field.
- 2–5 years of regulatory experience in the chemical industry, preferably with exposure to cosmetics, pharmaceuticals, and/or home care products.
- Solid knowledge of global chemical and product regulations (e.g., EU, US, APAC).
- Experience with regulatory databases and tools (e.g., IUCLID, ECHA REACH-IT, CosIng).
- Strong organizational, analytical, and communication skills.
- Detail-oriented with the ability to manage multiple priorities under tight deadlines.
Regulatory Affairs Specialist employer: Laborare Group Limited
Contact Detail:
Laborare Group Limited Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Specialist
✨Tip Number 1
Familiarise yourself with the specific regulations mentioned in the job description, such as REACH and CLP. Understanding these regulations will not only help you in interviews but also demonstrate your proactive approach to compliance.
✨Tip Number 2
Network with professionals in the regulatory affairs field, especially those who work in cosmetics, pharmaceuticals, or home care. Engaging with industry experts can provide insights into current trends and challenges, making you a more attractive candidate.
✨Tip Number 3
Stay updated on global chemical regulations by following relevant news sources and joining professional associations. This knowledge will be invaluable during discussions with potential employers and can set you apart from other candidates.
✨Tip Number 4
Prepare to discuss your experience with regulatory databases and tools like IUCLID and ECHA REACH-IT. Being able to articulate your hands-on experience with these tools will show that you're ready to hit the ground running in this role.
We think you need these skills to ace Regulatory Affairs Specialist
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of a Regulatory Affairs Specialist. Familiarise yourself with key regulations like REACH, CLP, and FDA to demonstrate your knowledge in your application.
Tailor Your CV: Highlight relevant experience in regulatory affairs, especially within the chemical industry. Emphasise your familiarity with global regulations and any specific tools or databases you've used, such as IUCLID or ECHA REACH-IT.
Craft a Compelling Cover Letter: Use your cover letter to showcase your passion for regulatory affairs and how your skills align with the job requirements. Mention specific examples of how you've ensured compliance in previous roles and your ability to work with cross-functional teams.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors. A detail-oriented approach is crucial for this role, so ensure your application reflects that quality.
How to prepare for a job interview at Laborare Group Limited
✨Know Your Regulations
Familiarise yourself with key regulations such as REACH, CLP, and FDA guidelines. Be prepared to discuss how these regulations impact product compliance and your previous experiences in navigating them.
✨Showcase Your Cross-Functional Experience
Highlight any experience you have working with teams like R&D, Marketing, and QA. Discuss specific projects where you coordinated efforts to ensure regulatory compliance, demonstrating your ability to collaborate effectively.
✨Prepare Regulatory Documentation Examples
Bring examples of regulatory documentation you've prepared, such as safety data sheets or product dossiers. This will showcase your attention to detail and understanding of the documentation process.
✨Stay Updated on Global Changes
Demonstrate your proactive approach by discussing how you keep abreast of changes in global regulations. Mention any tools or resources you use to monitor these changes and how you've applied this knowledge in past roles.
