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Manager, Quality Assurance GMP (12 month Fixed Term Contract)

CNX Therapeutics LtdHolborn, Central London

Salary
£47k – £47k
Posted
14 August 2026
Sponsor match
high
Skilled WorkerWorker (A rating)
Role overview

CNX Therapeutics Ltd is hiring a Manager, Quality Assurance GMP (12 month Fixed Term Contract) in Holborn, a scientific & qa role advertised as contract. The advertised salary is £47k – £47k. CNX Therapeutics Ltd 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.

Role Purpose The Manager, Quality Assurance GMP is responsible for leading GMP compliance, supplier assurance and product quality oversight activities across CNX Therapeutics. The role ensures that products manufactured, tested, released and distributed through third-party partners are managed in accordance with applicable GMP requirements, Market i ng Authorisation Holder obligations and company quality standards. The successful candidate will work closely with internal stakeholders, external …
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CNX Therapeutics Ltd 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: CNX Therapeutics Ltd — confirmed licensed sponsor
  • Visa route: Skilled Worker
  • Advertised salary: £47k – £47k
  • How this salary compares: about 17% above the £40,000 median across 859 scientific & qa roles with published salaries on FindSponsorJobs
  • Location: Holborn, Central London
  • Posted: 14 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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