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Jackson Hogg is exclusively partnered with a specialist scientific business in the Northumberland area, recruiting for a Regulatory Specialist position.
The Regulatory Specialist will be responsible for the following:
1. Managing submissions, maintenance, changes, and renewals for products under EU BPR, GB BPR, and other EMEA regulations according to market requirements.
2. Building IUCLID dossiers, using R4BP, preparing SPCs, submitting IUCLID dossiers, and Poison Centre Notifications.
3. Supporting Quality Assurance by implementing regulatory changes, such as label artwork and Change Controls.
4. Providing regulatory input for SDS preparation, marketing, sales, technical, and R&D teams.
5. Attending regulatory meetings in the EU and other regions as required.
6. Monitoring regulatory changes, including awareness of new regulations and updates to existing ones, and communicating potential impacts to the business.
7. Ensuring compliance with other chemical regulations like REACH, CLP, and Detergents, as applicable.
8. Submitting annual biocidal product sales quantities to relevant Member States.
9. Collaborating with departments, project teams, suppliers, testing laboratories, distributors, consultants, and Member State Authorities to coordinate regulatory submissions.
10. Supporting other sites with global registrations, e.g., USA and Australia.
11. Possessing IT skills in Word, PowerPoint, and Excel.
12. Proficient in IUCLID and R4BP.
13. Demonstrating good scientific communication skills, both written and oral.
Regulatory Specialist Requirements:
* Experience with human health toxicology, environmental risk, and exposure assessments.
* Experience with efficacy testing for regulatory purposes.
* Knowledge of CLP, REACH, SDS authoring, and regulatory labelling.
* Degree in a scientific field such as Chemistry or Pharmaceuticals.
* Essential experience within a regulatory position.
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