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Regulatory Affairs Specialist
4 months ago
I am seeking a highly motivated and experienced Regulatory Affairs Specialist with expertise within OTC/Cosmetics experience to join us on a contracted basis for a period of 6 to 12 months. As a key member of the Regulatory Affairs team, you will play a crucial role in ensuring our products comply with all relevant regulations and standards in various markets.
Like the look of this opportunity Make sure to apply fast, as a high volume of applications is expected Scroll down to read the complete job description.
Responsibilities:
- Conduct regulatory assessments and ensure compliance of cosmetic products with local and international regulations, including but not limited to FDA, EU, and other global regulatory agencies.
- Prepare and submit regulatory documents, including ingredient lists, safety assessments, and product dossiers, for product registrations and approvals.
- Stay up-to-date with changes in regulations and guidelines affecting the cosmetics industry and provide guidance to internal teams on compliance requirements.
- Collaborate cross-functionally with R&D, Quality Assurance, Marketing, and other departments to support product development and launch activities.
- Respond to regulatory inquiries and requests for information from regulatory authorities in a timely and accurate manner.
- Participate in regulatory audits and inspections, ensuring all documentation and processes meet regulatory requirements.
Qualifications:
- Bachelor’s degree in a scientific discipline or related field; advanced degree preferred.
- Minimum of 4-6 years of experience in regulatory affairs within the OTC/Cosmetics industry.
- In-depth knowledge of cosmetic regulations and guidelines, including experience with FDA, EU Cosmetics Regulation, and other global regulatory frameworks.
- Proven track record of successful product registrations and approvals in various markets.
- Strong attention to detail and excellent analytical skills.
- Ability to effectively communicate complex regulatory requirements to cross-functional teams.
- Experience with regulatory submissions and documentation management systems is preferred.
- Regulatory affairs certification or professional accreditation is a plus.
- MUST be based in the UK
Contract Details:
- Type: Contract, 6-12 months (with possibility of extension)
- Location: Hybrid/Remote (Circumstances dependant)
