Regulatory Specialist - Biocides & REACh Lisboa

Regulatory Specialist - Biocides & REACh
Lisboa
Lisboa, Lisboa, Portugal

Regulatory Affairs Specialist – Biocides & Medical Devices

Location: Portugal | Full-time Remote options available or on site if you prefer. Remote is 1 day per month in the office.

Our client is a leading
- owned chemicals group headquartered in Belgium, operating across 30 countries with over 1, 000 employees. With a consolidated turnover of approximately €400 million and a 15% annual growth rate over the last 15 years, the business is built on excellence, agility, and
- term vision. Their portfolio covers hygiene solutions for professional textile care, food processing, medical sectors, and more – offering
- quality detergents, disinfectants, and innovative equipment.

As part of their continued expansion and the increasing complexity of EU regulatory frameworks, they are now looking to strengthen their Corporate Registration Team in Portugal with an experienced Regulatory Affairs Specialist , focused on biocidal products.

Your Responsibilities:

Ensure continued compliance with EU and national chemical legislation.

Prepare and submit regulatory dossiers under the Biocidal Products Regulation (BPR) and support national authorisations.

Liaise with external partners (labs, consultants) for toxicological, efficacy, and risk assessments.

Maintain direct contact with regulatory authorities across Europe for dossier submissions and queries.

Collaborate with internal teams (R&D, Regulatory, Portfolio Management) to shape registration strategies and ensure timely execution.

Provide proactive guidance during product development regarding regulatory requirements.

Monitor and assess changes in EU and national legislation, keeping the business informed and aligned.

Engage in regulatory advocacy through industry associations to help shape future developments.

What We’re Looking For:

MSc or Ph
D in Chemistry, Biochemistry, Toxicology, or a related scientific field.

3–5 years’ experience in Regulatory Affairs within the chemical or related industries.

Strong understanding of EU regulatory frameworks: BPR, REACH, CLP, MDR.

Proven experience in dossier preparation and regulatory submissions.

Fluent English (spoken and written); additional languages are a plus.

Excellent organisational and project management skills.

Detail-oriented, analytical thinker with strong communication skills.

Self-driven, resilient, and capable of working both independently and in multicultural teams.

What’s on Offer:

A pivotal role in a stable,
- growth international company.

The opportunity to directly shape regulatory strategy and influence market access across Europe.

A collaborative environment with access to
- tier scientific and regulatory expertise.

Competitive remuneration package aligned with your experience and the responsibility of the role.

For more information, either apply for this position or send your CV to Abid Kanji to a. kanji@nonstopconsulting.com