CAREERS

Join Our Technical & Regulatory Affairs Team

We are expanding our core regulatory and technical governance team. Help us ensure complete supply chain integrity, substance compliance, and safety standards across bulk raw material distribution.

REGULATORY AFFAIRS • FULL-TIME

COMPLIANCE • FULL-TIME

QUALITY AUDITING • FULL-TIME

Senior Regulatory Toxicologist

REACH Specialist

Supply Chain Quality Auditor

We are seeking an experienced Senior Regulatory Toxicologist to join our organisation and provide authoritative leadership across toxicology, product safety, and global regulatory compliance. This role is central to ensuring our specialty chemicals and personal care ingredients meet international standards for human health and environmental protection.

Role Summary

The Senior Regulatory Toxicologist will lead toxicological hazard evaluations, oversee product safety classifications, and manage the creation and approval of high‑quality SDS and supporting documentation. You will act as a senior scientific advisor, guiding regulatory strategy, supporting market access, and ensuring compliance with EU/UK/Global frameworks including REACH, CLP, GHS, and Cosmetics Regulation.

Key Responsibilities

  • Provide expert leadership in toxicological assessment, hazard identification, and regulatory classification.

  • Deliver scientifically robust safety documentation including SDS, exposure scenarios, toxicological profiles, and risk assessments.

  • Support REACH/UK REACH compliance activities, including DNEL/PNEC derivation and dossier maintenance.

  • Advise internal teams and external partners on regulatory impacts, safe use, and product stewardship.

  • Ensure alignment with global regulatory frameworks and emerging scientific methodologies.

  • Uphold high standards of scientific integrity, documentation quality, and regulatory governance.


Qualifications & Experience

  • MSc/PhD in Toxicology or related discipline.

  • Significant experience in regulatory toxicology within chemicals, cosmetics, or personal care sectors.

  • Strong working knowledge of REACH, CLP, GHS, Cosmetics Regulation, and related global frameworks.

  • Proven ability to interpret complex toxicological data and communicate clearly to diverse stakeholders.


Why Join Us

This is a senior, high‑impact role within a growing regulatory function. You will shape toxicology strategy, influence product safety decisions, and contribute directly to global compliance and market access.

We are seeking a highly organised and detail‑driven REACH Specialist to support our regulatory compliance activities across EU and UK markets. This role is responsible for ensuring full alignment with REACH and UK REACH obligations, maintaining dossier accuracy, and supporting market access for our chemical and personal care portfolios.

Role Summary

The REACH Specialist will manage registration activities, maintain IUCLID dossiers, coordinate data gathering, and ensure compliance with all relevant regulatory requirements. You will work closely with regulatory, product stewardship, and commercial teams to deliver timely, accurate, and defensible regulatory submissions.

Key Responsibilities

  • Manage REACH/UK REACH registrations including dossier updates, inquiry submissions, and data coordination.

  • Maintain and update IUCLID datasets, CSR sections, and supporting documentation.

  • Coordinate testing strategies, data gap analysis, and communication with laboratories and external partners.

  • Support compliance with CLP, SDS authoring, and product classification activities.

  • Monitor regulatory changes and ensure proactive alignment with evolving requirements.

  • Provide internal guidance on REACH obligations, timelines, and data needs.

Qualifications & Experience

  • Degree in Chemistry, Regulatory Affairs, Toxicology, or related field.

  • Strong working knowledge of REACH and UK REACH processes.

  • Experience with IUCLID, SDS authoring, and regulatory submissions.

  • Excellent organisational skills and attention to detail.

We are recruiting a Supply Chain Quality Auditor to strengthen our quality assurance framework across suppliers, manufacturing partners, and distribution channels. This role ensures that all supply chain operations meet internal standards, regulatory requirements, and customer expectations.

Role Summary

The Supply Chain Quality Auditor will conduct supplier audits, evaluate quality systems, and ensure compliance with chemical, cosmetic, and personal care regulatory frameworks. You will play a critical role in maintaining product integrity, operational consistency, and supply chain reliability.

Key Responsibilities

  • Conduct supplier quality audits across manufacturing, packaging, and distribution partners.

  • Assess compliance with ISO standards, GMP, regulatory requirements, and internal quality policies.

  • Identify gaps, risks, and non‑conformities; develop corrective action plans with suppliers.

  • Monitor ongoing supplier performance and maintain audit documentation.

  • Collaborate with procurement, regulatory, and operations teams to ensure supply chain robustness.

  • Support continuous improvement initiatives across quality and compliance functions.

Qualifications & Experience

  • Background in Quality Assurance, Chemistry, Supply Chain, or related discipline.

  • Experience conducting audits within chemical, cosmetic, or manufacturing environments.

  • Strong understanding of ISO/GMP frameworks and supplier quality systems.

  • Excellent communication, documentation, and analytical skills.