Regulatory Specialist

Jackson Hogg are excluisvely partnered with a specialist scientific business in the Northumberland area on a Regulatory Specialist position.

The Regulatory Specialist will be responsible for the following:

• 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 business


• Maintain compliance with other chemical regulations e.g., REACH, CLP, Detergents, as applicable for the businesses 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 coordinate and monitor regulatory submissions and requirements


• Support other sites with global registrations e.g., USA and Australia


• IT Skills (Word, PowerPoint and Excel)


• Proficient in use of IUCLID and R4BP


• Good scientific communication (written and oral)

Regulatory Specialist Requirements�

• Experience with human health toxicology and environmental risk and exposure assessments


• Experience with efficacy testing for regulatory purposes


• Experience with CLP, REACH, SDS authoring and regulatory labelling


• Degree eduacated within a scientific field, Chemistry, Pharmaceutical etc�


• Experience within a regulatory position is essential�