Regulatory Affairs Specialist - Biocide Registration

Consult; Portugal; Teletrabalho; USD 35 034 - 70 069; Tempo integral

Resumo da oferta

An exciting opportunity awaits as a Regulatory Affairs Specialist in a global leader in the chemical industry. This role focuses on ensuring compliance with European and national chemical legislation, particularly in biocide and medical device registration. You will play a crucial role in preparing registration dossiers, supporting national authorizations, and collaborating with external service providers. If you're ready to make a significant impact and grow with a respected company, this position is perfect for you. Join a dynamic team and contribute to the ongoing success of a rapidly expanding organization.

Qualificações

• 1-4 years of experience in Regulatory Affairs, focusing on chemical legislation.
• Proficient in English and Portuguese with strong analytical skills.

Responsabilidades

• Prepare and submit registration dossiers for BPR and MDR compliance.
• Work with external providers for testing and risk assessments.

Conhecimentos

Regulatory Affairs

Analytical Skills

Attention to Detail

English

Portuguese

Descrição da oferta de emprego

Regulatory Affairs Specialist - Biocide Registration

Location: Portugal (remote)

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 physical-chemical, efficacy, toxicological tests, and risk assessments.
• Provide guidance on registration requirements to R&D during new product developments.
• Stay up-to-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.

Seniority level: Associate

Employment type: Full-time

Job function: Other

Industries: Chemical Manufacturing