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- 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.
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. Attend industry events or join relevant online forums to gain insights and make connections that could lead to job opportunities.
✨Tip Number 3
Showcase your experience with regulatory databases and tools like IUCLID or ECHA REACH-IT during conversations. Being able to discuss your hands-on experience with these tools can set you apart from other candidates.
✨Tip Number 4
Prepare to discuss how you've contributed to continuous improvement in regulatory processes in your previous roles. Highlighting specific examples of how you've streamlined processes or improved compliance can impress potential employers.
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: Customise your CV to highlight relevant experience in regulatory affairs, particularly in the chemical industry. Emphasise any specific projects or roles where you ensured compliance with regulations related to cosmetics, pharmaceuticals, or home care products.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for regulatory affairs and your understanding of global chemical regulations. Mention specific experiences that align with the job description and how you can contribute to the company's success.
Highlight Soft Skills: In your application, don't forget to mention your strong organisational, analytical, and communication skills. Provide examples of how you've managed multiple priorities under tight deadlines, as this is crucial for the role.
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 share examples of your experience in navigating them.
✨Showcase Your Cross-Functional Experience
Highlight your ability to work with various teams like R&D, Marketing, and QA. Prepare specific examples of how you've successfully coordinated with different departments to ensure regulatory compliance.
✨Demonstrate Attention to Detail
As a Regulatory Affairs Specialist, attention to detail is crucial. Bring examples of how your meticulous nature has helped in preparing regulatory documentation or managing submissions effectively.
✨Stay Updated on Global Changes
Discuss how you keep abreast of changes in global regulations. Mention any tools or databases you use, and be ready to explain how you've assessed the impact of regulatory changes on previous projects.
