Regulatory Affairs Specialist

REGULATORY AFFAIRS SPECIALIST

• Location: Redditch
• Salary: £38,.000 - £45,000
• Contract: Permanent
• Working hours: Days
• Well known established brand
• Bupa
• Bonus paid Quarterly
• Hybrid working offered (80/20 - must be Midlands based)
• Cycle to work scheme
• Death in Service

Ready to make your mark in Regulatory Affairs?

We're looking for an experienced Regulatory Affairs Specialist to join a growing team and take ownership of chemical classification, SDS authoring, product labelling and regulatory compliance across a diverse product portfolio.

This is a hands-on role where your expertise in CLP/GHS, SDSs, PCNs and UFI codes will make a real impact - working closely with R&D, Quality, Operations, Commercial and Marketing teams to keep products compliant and moving forward.

Commutable from Redditch, Birmingham, Studley, Worcester, Droitwich, Alcester, Stratford-Upon-Avon, Knowle, Solihull, Warwick, Halesowen, Bromsgrove and Balsall Common

Duties

• Classify products under EU CLP, GB CLP and GHS, ensuring accurate hazard classifications and labelling.
• Author, review and maintain SDSs for formulated products, using Lisam ExESS or equivalent.
• Manage Poison Centre Notifications (PCNs) and UFI codes, including submissions and updates.
• Review and approve product artwork, labels and packaging for regulatory compliance.
• Assess the regulatory impact of formulation changes, raw material substitutions and new product development.
• Ensure classifications are accurately reflected across SDSs, labels, technical documentation and marketing materials.
• Keep on top of changing chemical regulations and identify their impact on the product portfolio.
• Provide expert regulatory advice to colleagues across the business.
• Support process improvements, SOP development and regulatory training.

Requirements

• It is essential to have experience in Regulatory Affairs.
• Strong, demonstrable CLP classification expertise.
• Solid SDS authoring experience using Lisam ExESS or equivalent.
• Hands on experience managing PCN submissions and UFI codes.
• Knowledge of EU/UK chemical regulatory requirements.
• Strong attention to detail with the confidence to provide expert regulatory guidance across the business.

Why join?

This is a great opportunity for an experienced Regulatory Affairs professional to take ownership of a key compliance function, work across multiple areas of the business and play an important role in shaping regulatory processes as the product portfolio develops.

If CLP, SDS, PCN and UFI are your area of expertise, we'd love to hear from you.

Please Note: Candidates must have the right to live and work in the UK.