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An established industry player in regulatory affairs is seeking a Senior Biocide Regulatory Specialist. This role offers the chance to lead consultancy projects, develop regulatory strategies, and engage with stakeholders. With a focus on career progression and flexible working arrangements, this consultancy provides a dynamic environment for high-performing professionals. Join a team that values innovation and offers opportunities for professional development, while making a significant impact in the biocide regulatory landscape. If you're ready to advance your career in a supportive and growing organization, this position is an exciting opportunity for you.
Full time | Blue Frog Scientific Limited | United Kingdom
Posted On 03/14/2025
Chemicals
Work Experience 5+ years
Competitive, based on experience
City Edinburgh
Province City of Edinburgh
Postal Code EH1 1AE
Blue Frog Scientific is a leading regulatory affairs consultancy, specialising in the registration and compliance of biocides, chemicals, pharmaceuticals, and plant protection products. As a growing organisation we are now seeking a Senior Biocide Regulatory Specialist to join our dynamic team.
This role provides the opportunity to take the lead on consultancy projects for active substance and biocidal product registrations in addition to advocacy work to defend substances subject to renewal challenges or other regulatory pressures. As a growing organisation, there is ample opportunity for career progression for high-performing staff.
We have offices in Edinburgh, Swansea (United Kingdom), and Lyon (France). We'd be happy to accommodate you at any of our offices, or the position can be fully remote in the United Kingdom or France.
Biocidal Regulatory Consultancy: Provide high-level regulatory consultancy under the Biocidal Products Regulation (EU) 528/2012 and equivalent GB/NI regulation.
Regulatory Strategy Development: Provide strategic regulatory advice on EU and UK regulatory requirements, using creative and innovative approaches to improve the cost-benefit to our clients.
Dossier Preparation & Submission: Coordinate the compilation of active substance and biocidal product dossiers for EU and GB submission.
Advocacy & Stakeholder Engagement: Liaise with regulatory authorities (EFSA, CRD, ECHA) and participate in expert groups, workshops, and regulatory consultations.
Project & Client Management: Lead client projects, ensuring high-quality, timely deliverables and maintaining strong client relationships.
Essential Qualifications & Experience:
What We Offer:
How to Apply:
Please send your CV and a cover letter outlining your experience and interest in the role.