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Open nowFirst seen 68 days ago

Regulatory Affairs Specialist

Arxada55 open roles

Where
UK - Manchester
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Your applicationOpen nowRegulatory Affairs SpecialistArxada · UK - Manchester

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The clock on this job

Early applications get read.

12.3% of postings close within 7 days. Measured by our own scanner across the market. Arxada postings stay open a median of 49 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.3%7 days
  4. 19.3%14 days
  5. 35.6%30 days
  6. 57.8%60 days
This job: first seen 68 days ago

Arxada median: 49 days open

The posting

Arxada is a global leader in innovative solutions that protect our world. Our groundbreaking technologies, in-depth regulatory know-how, manufacturing and process development help our customers to safeguard nutrition, health and infrastructure efficiently through chemistry and biotechnology that enhance sustainability. We offer a broad portfolio of ingredients and services for multiple end-markets that include Human Health & Nutrition, Home & Personal Care, Professional Hygiene, Paints & Coatings and Wood Protection. With customers in more than 100 countries, the company achieved sales of CHF 2 billion in 2024. Headquartered in Basel (Switzerland), Arxada employs 3,200 associates across 24 production sites and 14 R&D centers, all committed to our customers’ success.

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. Collaborating closely in a matrix environment, this role offers the opportunity to make a tangible impact across multiple product areas while helping Arxada go beyond in delivering sustainable, science‑led solutions.

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 has world class offering in two distinct areas: Microbial Control Solutions (MCS) focuses on threats posed by microorganisms to people and planet through five distinct business lines including Professional Hygiene, Home & Personal Care, Wood Protection, Paints & Coatings and Material Protection. Nutrition, Care & Environmental (NCE), meanwhile, provides materials used to manufacture composites for electronics, aerospace and other markets, as well as vitamins and nutritional ingredients, chemicals and performance intermediates, and raw materials for a wide range of high‑performance applications. 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.

GB08

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