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 forproducts 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