THE COMPANY

Our client is a specialist in the manufacturer for the pharmaceutical sector. Due to growth, they are now looking to recruit a Regulatory Specialist.

• Manage and maintain EU, GB and EMEA authorisations of biocidal products; ensure compliance with other chemical regulations where applicable e.g. CLP; manage and maintain transitional biocidal registrations.
• Submission, maintenance, changes and renewals for products under EU BPR, GB BPR and other EMEA regulations as per market requirements.
• IUCLID dossier build, use of R4BP, preparation of SPCs, submission of IUCLID dossiers, preparation and submission of Poison Centre Notifications.
• Supporting Quality Assurance with implementing regulatory changes e.g. label artwork and Change Controls.
• Providing regulatory input for SDS preparation, marketing, sales, technical and R&D.
• Attend regulatory meetings in EU and elsewhere as required.
• Regulatory monitoring, including awareness of new regulations and changes to existing regulations, including internal communication of any potential impact to the company.
• Maintain compliance with other chemical regulations e.g., REACH, CLP, Detergents, as applicable for product range.
• Submission of annual biocidal product sales quantities to selected Member States.
• Liaise with all departments, project teams, suppliers, testing laboratories, distributors, consultants and Member State Competent Authorities to co-ordinate and monitor regulatory submissions and requirements
• Support other group sites with global disinfectant registrations.
• Could be full time or part time depending on the person.
• Could also offer remote working but site visits at least once a month or expected.

The Person

• Will have experience within a similar role.
• Must have biocides and BPR experience.
• You will have good IT Skills (Word, PowerPoint and Excel).
• Be proficient in use of IUCLID and R4BP.
• Good scientific communication (written and oral).
• Experience with human health toxicology and environmental risk and exposure assessments would be desirable.
• Experience with efficacy testing for regulatory purposes is desirable.
• Experience with CLP, REACH, SDS authoring and regulatory labelling would be beneficial.