Job Title: Regulatory Affairs Consultant (M&A)
Company: Christeyns
Location: Nantes, France
Duration: 6 months, Full-time (3 days a week on-site)
Start Date: Late November (1) / Mid December (2)
Budget: To Be Confirmed
Job Description:
About Us: Christeyns is a leading company in the development and sale of detergents, biocides, and cosmetic products, including soaps and Hair & Body products. We are located near Nantes, France.
Job Description: We are seeking 1 or 2 experienced Regulatory Affairs Consultants to join our team on a temporary basis. This role is crucial as two of our current team members will be leaving by the end of the year. The consultants will be responsible for managing regulatory affairs activities to ensure compliance and support our product development and marketing efforts.
Key Responsibilities:
- Establish Safety Data Sheets (SDS) using ExESS software.
- Handle declarations to poison control centres.
- Manage BioCid registrations.
- Create and review labels in collaboration with R&D and Marketing teams.
- Enter data into the ERP software for ADR, CLP, ICPE, TGAP, and customs nomenclature.
- Participate in the preparation of Biocidal Products Regulation (BPR) files with colleagues from our Group in Belgium.
- Conduct regulatory watch and perform gap analysis and action plans related to biocides regulations, REACh, CLP, detergents, explosives precursors, etc.
- Handle PIC declarations.
Requirements:
- Fluency in French.
- Proven experience in regulatory affairs, preferably in the chemical or cosmetics industry.
- Familiarity with ExESS software and ERP systems.
- Strong understanding of relevant regulations (biocides, REACh, CLP, detergents, explosives precursors).
- Excellent communication and teamwork skills.
- Ability to work on-site in Nantes, France, for 3 days a week.
