As a Regulatory Affairs Specialist based in Manchester, UK (hybrid, part‑time), you will play a vital role in enabling Arxada’s continued growth and market access across the EMEA region. Working within the Microbial Control Solutions business area, you will contribute regulatory expertise that supports business continuity, customer confidence, and compliant innovation.
Essential Job Functions
- Deliver regulatory aspects of business‑critical projects such as coordination and submission of EMEA biocidal product and/or active substance dossiers to achieve registrations.
- Manage post‑submission activities to drive favorable outcomes, including engagement with regulatory authorities and other stakeholders.
- Provide clear regulatory expertise, policy analysis, and advice to internal stakeholders and customers.
- Partner cross‑functionally with Marketing, Sales, R&D, Quality, and Product Safety teams to support strategic and technical regulatory objectives.
- Monitor and communicate regulatory changes and assess their impact on the product portfolio.
- Demonstrate flexibility, resilience, and a collaborative mindset to support broader regulatory team goals.
Qualifications & Experience
- Bachelor’s degree in Life Sciences, Chemistry, or a related field, or equivalent demonstrable working experience.
- Min. 1+ years experience in Regulatory Affairs within biocides.
- Working knowledge of BPR, CLP, REACH, and related regulatory frameworks.
- Hands‑on experience with IUCLID and R4BP3.
- Strong attention to detail with the ability to translate complex regulatory topics for non‑experts.
- Proactive, commercially aware, and comfortable managing multiple priorities in a matrix environment.
Arxada is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
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