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About Us
Randstad II - Prestação de Serviços, Limitada is a chemical group with global operations. We are seeking an experienced Regulatory Affairs Specialist to strengthen our team.
Job Summary
The successful candidate will be responsible for preparing and submitting biocide and medical device registration dossiers in accordance with European regulations, including BPR and MDR.
Main Responsibilities
- Maintain company compliance with regional and national chemicals legislation.
- Prepare and submit registration dossiers for biocidal products and medical devices.
- Interact with external service providers and authorities to obtain necessary approvals.
- Collaborate with internal stakeholders to drive decision-making and provide expert knowledge.
- Provide guidance on registration requirements during new product development.
- Stay informed about regulatory developments and assess their impact on the company.
- Participate in advocacy efforts to influence regulatory changes.
Requirements
- A Master's or PhD degree in Chemistry, Biochemistry, Toxicology, or Ecotoxicology.
- 3-5 years of experience in Regulatory Affairs within the chemical industry.
- Familiarity with chemical legislation, such as BPR, CLP, REACH, and PPPR.
- Strong project management skills and attention to detail.
- Excellent analytical and communication skills.
Benefits
An attractive remuneration package is offered for this position.
