Regulatory Affairs Specialist

Probe UK; Holt End; Hybrid; GBP 38,000 - 45,000; Full time

Benefits offered by this job

Bupa

Quarterly bonus

Cycle to work

Death in service

Job summary

Probe UK is seeking a Regulatory Affairs Specialist to own regulatory compliance across a diverse product portfolio. You will manage CLP/GHS classifications, author SDS and maintain PCNs and UFI codes, collaborating with R&D, Quality, Operations and Marketing to keep products compliant.

Based in the Midlands with 80/20 hybrid working, you will assess regulatory changes, review artwork and packaging, and provide expert guidance across the business. UK right to work is required.

Qualifications

• Experience in Regulatory Affairs and chemical regulations.
• Strong CLP/GHS classification expertise.
• SDS authoring using Lisam ExESS or equivalent.
• Hands-on PCN submissions and UFI code management.
• Knowledge of EU/UK chemical regulatory requirements.
• Ability to provide expert regulatory guidance across the business.

Responsibilities

• Classify products under EU CLP, GB CLP and GHS with accurate labeling.
• Author/review and maintain SDSs for formulated products.
• Manage PCNs and UFI codes, including submissions and updates.
• Review artwork, labels and packaging for regulatory compliance.
• Assess regulatory impact of formulation changes and new products.
• Ensure classifications are reflected across SDSs, labels and tech docs.

Skills

Regulatory Affairs

CLP classification

SDS authoring

PCN submissions

UFI codes

UK/EU chemical regulations

Tools

Lisam ExESS

Job description

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.