Regulatory Affairs Lead: CLP, SDS & Compliance

Smart4 Sciences; Redditch; On-site; GBP 45,000 - 65,000; Full time

Job summary

Smart4 Sciences in the United Kingdom is seeking a Regulatory Affairs Specialist to lead CLP classification and SDS authoring, supporting product compliance from concept to market launch.

Working with R&D, Quality and Manufacturing, you will prepare SDS, classify products, review labels and packaging, manage PCNs and UFI submissions, and monitor regulatory changes to keep products compliant across UK and EU markets.

Qualifications

• Previous experience within a Regulatory Affairs position.
• Strong knowledge of CLP classification and chemical regulations.
• Experience authoring and maintaining Safety Data Sheets.
• Exposure to PCN submissions and UFI management.
• Excellent attention to detail and documentation skills.
• The ability to communicate complex regulatory requirements to non-technical stakeholders.

Responsibilities

• Prepare, review and maintain Safety Data Sheets (SDS) for a diverse product portfolio.
• Classify products in accordance with CLP, GHS and UK regulatory requirements.
• Assess formulation changes and determine regulatory impact.
• Review supplier documentation and evaluate compliance implications.
• Approve product labels, packaging artwork and regulatory claims.
• Manage Poison Centre Notifications (PCNs) and UFI submissions.
• Ensure regulatory information remains consistent across labels, SDSs and technical documentation.
• Support internal teams with regulatory advice and compliance guidance.
• Monitor emerging legislation and communicate potential business impacts.
• Contribute to continuous improvement initiatives and regulatory best practice.

Skills

CLP classification

SDS authoring

Regulatory guidance

PCN submissions

UFI management

Documentation skills

Job description

Smart4 Sciences in the United Kingdom is seeking a Regulatory Affairs Specialist to lead CLP classification and SDS authoring, supporting product compliance from concept to market launch.

Working with R&D, Quality and Manufacturing, you will prepare SDS, classify products, review labels and packaging, manage PCNs and UFI submissions, and monitor regulatory changes to keep products compliant across UK and EU markets.