Quality Assurance Auditor

16h16 hours ago

SGS

Glasgow, GB · Full-time · £24,603 – £30,000

About this role

As a Quality Assurance Auditor at SGS, you review final reports to ensure all laboratory methods, procedures, observations, and results are accurately documented and consistent with raw data. You communicate any issues found during data checks to the Study Director, Principal Investigator, and relevant management.

Your day-to-day involves verifying final reports and raw data for accuracy, completeness, and GLP/GMP compliance. You prepare and maintain all quality documentation, including approved study documents and SOPs, while planning your workload to ensure efficient auditing.

You work within SGS's Life Sciences team, supporting pharmaceutical and biotech sectors with expert testing and auditing. You provide compliance guidance to staff and liaise with clients on deviations, investigations, and CAPAs, ensuring regulatory standards are met.

At SGS, you join a global network of 100,000 employees committed to quality and integrity. This role offers the chance to develop deep expertise in pharmaceutical quality assurance within a leading Life Sciences organization.

Requirements

Degree in Biomedical Sciences, Life Sciences, or a related field (industry experience or placement beneficial).
Strong attention to detail and high auditing standards.
Ability to review data and draw clear, accurate conclusions.
Experience with database management.
Strong IT skills (Word, Excel, PowerPoint).
Familiarity with business and regulatory guidelines.
Effective communication skills.
Solid analytical reasoning and numerical ability.

Responsibilities

Review and verify final reports and raw data for accuracy, completeness, and compliance with GLP and GMP standards.
Communicate findings promptly to study leadership and management.
Prepare, manage, and maintain all quality documentation, including approved study documents and SOPs.
Ensure all study documentation meets regulatory and compliance requirements.
Plan and prioritise workload to ensure efficient auditing and adequate resource allocation.
Provide compliance guidance to staff and support Study Directors with issue resolution and client discussions.
Liaise with clients on deviations, investigations, or out‑of‑specification events, ensuring effective implementation of CAPAs.