regulatory affairs specialist.

• As a member of the registration team having the joint responsibility for maintaining company’ continued compliance with European regional and national chemicals legislation.


• Responsible for preparation and submission of registration dossiers in the framework of the Biocidal Products Regulation, supporting both national authorizations (pre-BPR) as well as obtaining approvals to BPR.


• Interact with external services providers (consultants and laboratories) for the generation of physical-chemical and efficacy tests, toxicological tests and risk assessments.


• Interact with authorities on existing and future submissions.


• Interact with internal stakeholders (Regulatory, R&D, Portfolio Management, Application Management) providing input to the registration dossiers. Drive decision making by proposing registration strategies, maintaining adherence to deadlines and providing expert knowledge of what is feasible.


• Provide guidance on registration requirements to R&D during new product developments.


• Maintain informed about developments in national and European (biocide) regulation. Assess the potential impact to the company and alert internal stakeholders.


• Participate in advocacy (e.g. via trade associations) in an effort to influence regulatory developments in order to minimize impact.

• A University Degree in Scientific background: Master or PhD, in Chemistry, Biochemistry, Toxicology. Ecotoxicology.


• 3 to 5 of industry experience within Regulatory Affairs (registration, development, maintenance).


• Experienced in Chemical Legislation, Chemical industry, Chemical Regulations (i.e. BPR, CLP, REACH, PPPR) & preparing regulatory dossiers.


• Proficiency in spoken and written English, knowledge of any other languages would be an asset.


• Project management skills, follow-through and hands on approach.


• Attention to detail and meeting deadlines.


• Analytical mind.

An excellent remuneration package, in line with the responsibility of this position.