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Scientific & QA Jobs

Chemical Regulatory Data Specialist - Contract Role 12 months

SynthomerHarlow, Essex

Salary
£49k – £49k
Posted
30 August 2026
Work mode
Full-time
Sponsor match
high
Skilled WorkerWorker (A rating)
Role overview

Synthomer is hiring a Chemical Regulatory Data Specialist - Contract Role 12 months in Harlow, a full-time scientific & qa role advertised as contract. The advertised salary is £49k – £49k. Synthomer holds an active licence on the UK Home Office register of sponsors for the Skilled Worker route, which means it can sponsor a visa for this hire if it chooses to.

Synthomer is a leading supplier of high-performance, highly specialised polymers and ingredients that play vital roles in key sectors such as coatings, construction, adhesives, and health and protection – growing markets that serve billions of end users worldwide. Headquartered in London, UK and publicly listed there since 1971, we employ c.3,900 employees across our 5 innovation centres of excellence and more than 29 manufacturing sites across Europe, North America and Asia. Around 20% of our …
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Synthomer is confirmed on the UK Home Office register of licensed sponsors for the Skilled Worker visa route (Worker (A rating)). Always confirm sponsorship availability for this specific role directly with the employer when you apply.
Visa sponsorship snapshot
  • Employer: Synthomer — confirmed licensed sponsor
  • Visa route: Skilled Worker
  • Advertised salary: £49k – £49k
  • How this salary compares: about 21% above the £40,675 median across 718 scientific & qa roles with published salaries on FindSponsorJobs
  • Location: Harlow, Essex · Full-time
  • Posted: 30 August 2026
  • How we verify sponsors: employers are matched against the UK Home Office register of licensed sponsors — read our methodology.
About this sector

Scientific and quality assurance roles span pharmaceutical, biotech, clinical research, and laboratory sectors. The UK life sciences industry actively recruits internationally for research scientists, QA managers, regulatory affairs specialists, and clinical trial coordinators, with many employers maintaining well-established sponsor licence operations.

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