Regulatory Affairs Specialist – CLP, SDS & UFI Expert

Smart4 Sciences; Redditch; On-site; GBP 50,000 - 65,000; Full time

Job summary

Smart4 Sciences is seeking a Regulatory Affairs Specialist to join its on-site team in Redditch. The role focuses on UK and EU chemical regulations, CLP classification, SDS authoring, and providing regulatory support across R&D, Quality and Manufacturing.

You will navigate regulatory changes and guide multiple departments to maintain compliant products. You will work closely with cross-functional teams to ensure accurate labeling, artwork approval, and regulatory claims across the product

Qualifications

• Strong knowledge of CLP classification and chemical regulations.
• Experience authoring and maintaining Safety Data Sheets.
• Exposure to PCN submissions and UFI management.

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

PCN submissions

UFI management

Regulatory guidance

Job description

Smart4 Sciences is seeking a Regulatory Affairs Specialist to join its on-site team in Redditch. The role focuses on UK and EU chemical regulations, CLP classification, SDS authoring, and providing regulatory support across R&D, Quality and Manufacturing.

You will navigate regulatory changes and guide multiple departments to maintain compliant products. You will work closely with cross-functional teams to ensure accurate labeling, artwork approval, and regulatory claims across the product