This job is now closed.

Quality Audior

Reference: BBBH28333
Date posted: 20/01/2026
Job details
Specialism
Technical Operations
Expertise
Quality Control
Location
City of London, London, England
Job type
Contract
Register your interest

If you can’t find your ideal role with us right now, we’d still love to hear from you! Send us your CV and we’ll contact you if a suitable role becomes available.

Register interest

Description

Step into a role where your attention to detail doesn’t just matter, it drives the integrity of life‑changing medicines with this Quality Auditor role!

R&D Partners is seeking a Quality Auditor to be responsible for reviewing clinical batch records to ensure they meet Good Manufacturing Practices (GMP) and regulatory standards. You will compile and approve data packs and collaborate with global teams and manufacturing sites to support the clinical supply chain. This position requires strong communication skills, attention to detail, and the ability to work independently.

Please note that to be considered for this role you must have the right to work in this location

Responsibilities:

  • Review clinical batch records to ensure compliance with GMP and regulatory requirements.
  • Compile and approve data packs for presentation to the Qualified Person (QP) for final release.
  • Conduct routine audits of data, procedures, equipment, and systems to ensure compliance with regulations.
  • Review and approve production and analytical documentation for clinical supply lots.
  • Communicate and resolve audit findings with relevant teams.
  • Perform inspections or audits to assess compliance and issue reports summarizing findings.
  • Collaborate with teams to address deficiencies and implement corrective actions.

Key Skills and Requirements:

  • Knowledge of GMP regulations and experience in the pharmaceutical industry or a regulatory agency.
  • Strong attention to detail and problem-solving skills.
  • Effective written and verbal communication skills.
  • Ability to manage multiple tasks and projects efficiently.
  • Proficiency in Microsoft applications and willingness to learn GMP-related software.
  • Bachelor’s degree in a life sciences field or related discipline.

For more information, please contact Grant Van Schalkwyk.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you’ve read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.r-dpartners.com/privacy-policy/

Register your interest

If you can’t find your ideal role with us right now, we’d still love to hear from you! Send us your CV and we’ll contact you if a suitable role becomes available.

Register interest

Related jobs

Discover our latest opportunities in life sciences and apply now.

View all jobs

Get in touch

Have questions or need support? Our team is here to help, contact us to discuss your hiring needs or career goals today.

Contact us