Regulatory ant

Do you have experience in the registration of Chemicals under EU-REACH and feel particularly at home across all sections of dossiers?

Looking to leverage that experience in a global structure where you will be working 80% remote and collaborating with fellow regulatory experts in the team across different global regulations?

This opportunity might interest you

We are partnering with a global chemical consulting firm renowned for its expertise in regulatory compliance across America, Asia, and Europe (including the UK). With a strong focus on chemical registrations and compliance on particularly complex projects within the EU-REACH, UK-REACH, TSCA, KKDIK and K-REACH frameworks, assisting clients in navigating complex and ever evolving regulatory landscapes to bring chemical products to market safely and efficiently.

The Role

As a Regulatory Affairs Consultant, you will play a critical role in chemical registrations and regulatory dossier submissions, working within a flexible hybrid model (only one day per week required in the Brussels office).

This role offers an exciting opportunity to interpret scientific data, ensure regulatory compliance, and contribute to international chemical regulations. If you have some strong knowledge in toxicology, this role will also allow you to fully express yourself in this area

The position is one where Science really meets Regulation

Key Responsibilities

• Chemical Registrations & Compliance: Manage and support substance registrations under EU REACH, with occasional involvement in UK-REACH and TSCA.
• Regulatory Dossier Preparation & Submission: Assist in compiling, reviewing, and submitting registration dossiers, ensuring accuracy and adherence to regulatory requirements.
• Scientific Data Interpretation: Analyze complex toxicological and environmental data to support regulatory decisions.
• IUCLID Software Utilization: Use IUCLID for data input and management, ensuring compliance with regulatory standards.
• Stakeholder Collaboration: Work closely with internal regulatory teams and external clients to support successful product registrations.
• Regulatory Updates & Compliance Monitoring: Stay informed about evolving chemical regulations and assess their impact on company operations.

Your Profile

• 3+ years of experience in chemical regulatory affairs, particularly in substance registration.
• Strong proficiency in IUCLID and experience working with chemical registration dossiers.
• Good knowledge of toxicology and an understanding of how it applies to regulatory assessments.
• A scientific academic background (e.g., Chemistry, Environmental Science, Toxicology, or a related field).
• A detail-oriented approach with the ability to interpret complex regulatory requirements.
• Excellent organizational and communication skills, with the ability to collaborate across teams.

What's in It for You?

• Work for a globally recognized regulatory consulting firm with a strong industry reputation for excellence
• Flexible hybrid work model – only one day per week required in the Brussels office.
• Career growth opportunities in an expanding international organization.
• Exposure to global regulatory frameworks, enhancing your professional expertise.
• Competitive salary and benefits package, aligned with your experience and skills.

In order to be eligible for this position, you need to justify of the ability of being present once per week in Brussels (if applying from outside of Belgium), and have full rights to work within the Shenghen area.

Interested?

Apply now, and we will be in touch with you very soon