Regulatory Affairs Specialist - Biocide Registration Setúbal

Regulatory Affairs Specialist - Biocide Registration
Setúbal
Setúbal, Setubal, Portugal

Regulatory Affairs Specialist - Biocide Registration
Location: Portugal (remote) or hybrid in Lisbon
Competitive Salary + Benefits
Scope:Our client, in the chemicals sector, is looking to strengthen its Regulatory Affairs Department due to rapid company growth and increasingly complex regulatory environments. As a Regulatory Affairs Specialist, you will be responsible for ensuring compliance with European and national chemical legislation, focusing on biocide and medical device registration dossiers. This is an exciting opportunity to make a significant impact at the forefront of regulatory compliance and contribute to the ongoing growth of a highly respected global company. Key Responsibilities:Prepare and submit registration dossiers for Biocidal Products Regulation (BPR) and Medical Device Regulation (MDR) compliance. Support both national authorizations (pre-BPR) and the process to obtain approvals to BPR. Work with external service providers (consultants, laboratories) for testing, including
- chemical, efficacy, toxicological tests, and risk assessments. Provide guidance on registration requirements to R&D during new product developments. Stay
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- date on European and national regulatory developments and evaluate their impacts. About You:1-4 years of experience within Regulatory Affairs, specifically in chemical legislation (e. g. , BPR, CLP, REACH, PPPR) and dossier preparation. Proficient in English and Portuguese
Excellent analytical skills and attention to detail. How to Apply:If you’re looking to take on a rewarding challenge and contribute to a global leader in the chemical industry, click apply or contact us for more information. Consult will endeavour to contact candidates within 14 days of application. However, if you do not hear back after 2 weeks, unfortunately, you have not been successful on this occasion.