Biocidal Regulatory Affairs Specialist (Efficacy/APCP)

Redebel SA; Belgique; À distance; EUR 60 000 - 90 000; Plein temps

Résumé du poste

Redebel SA, based in Belgium, seeks a Regulatory Affairs Consultant focused on Biocidal products with Efficacy or APCP expertise. The role involves ensuring products meet EU regulations, performing health risk assessments, and preparing regulatory dossiers.

You will work with cross-functional teams and manage projects independently in a dynamic environment. The ideal candidate has 2–5 years in regulatory affairs, expertise in efficacy or APCP, and a Master’s in science, with strong communication

Qualifications

• 2–5 years of regulatory affairs experience, preferably biocidal products.
• Master's degree in science or related field.
• Strong toxicology skills and knowledge of EU biocidal regulations.
• Excellent communication and cross-functional collaboration.

Responsabilités

• Ensure that clients' products meet regulatory requirements and reach the market quickly and efficiently.
• Conduct human health risk assessments.
• Prepare and submit regulatory dossiers for biocidal products.
• Coordinate with internal teams and external stakeholders, and manage projects independently.
• Assist in other regulatory tasks as needed.

Connaissances

Regulatory affairs

Biocidal products

Toxicology

EU regulations

Project management

Formation

Master's in Science

Description du poste

Redebel SA, based in Belgium, seeks a Regulatory Affairs Consultant focused on Biocidal products with Efficacy or APCP expertise. The role involves ensuring products meet EU regulations, performing health risk assessments, and preparing regulatory dossiers.

You will work with cross-functional teams and manage projects independently in a dynamic environment. The ideal candidate has 2–5 years in regulatory affairs, expertise in efficacy or APCP, and a Master’s in science, with strong communication