Job Title: Quality Auditor (Onsite – London)
We have an exciting opportunity for a Quality Auditor to join a leading Global Development Quality team on a 6-month contract based onsite in London.
About the Role
This position offers exposure to a wide range of investigational medicinal products, from small molecules to advanced immunotherapy treatments. You will play a key role in ensuring GMP compliance and regulatory conformance by reviewing clinical batch records and supporting QP release.
Key Responsibilities
* Conduct GMP audits of data, systems, and facilities.
* Review and approve production and analytical documentation.
* Work closely with global teams to resolve compliance issues.
* Assess and report regulatory deficiencies, supporting remedial actions.
Who We’re Looking For
* Experience in QA/GMP compliance within the pharmaceutical/chemical industry or regulatory agencies.
* Strong attention to detail and ability to work independently.
* Excellent communication and problem-solving skills.
* Open to new science graduates (Bachelor’s degree minimum) with a proactive mindset and willingness to learn.
Start Date: Beginning of March 2025
Location: London (Fully Onsite)
Duration: 6 months
If you're interested, apply now or reach out for more details!
nfordyce@barringtonjames.com