Quality Assurance Auditor at SGS

Clydebank, Scotland, United Kingdom -

Full Time

Start Date

Immediate

Expiry Date

17 Sep, 26

Salary

0.0

Posted On

19 Jun, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Auditing, GLP Compliance, GMP Compliance, Data Verification, Report Review, SOP Management, CAPA Implementation, Database Management, Analytical Reasoning, Numerical Ability, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Regulatory Compliance, Communication Skills, Attention To Detail

Industry

Professional Services

Description

Company Description We are SGS – the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 100,000 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world. Our brand promise – when you need to be sure – underscores our commitment to trust, integrity and reliability. SGS’s Life Sciences services support the pharmaceutical, biotech, and healthcare sectors with expert testing, clinical research, auditing, and certification—ensuring product safety, quality, and regulatory compliance from development to market. Job Description Role: Quality Assurance Auditor Job Type: Permanent Location: Glasgow Salary: From £25,000 Hours: 35 hours, Monday to Friday 9:00am-5:00pm Industry: Life Science Role Overview As a Quality Assurance Auditor, you will review final reports to ensure all laboratory methods, procedures, observations, and results are accurately documented and consistent with raw data. You will communicate any issues found during data checks to the Study Director/Scientist, Principal Investigator, and relevant management. Key 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. Qualifications 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. Additional Information At SGS, we believe in rewarding our employees for their hard work and commitment. As part of our team, you would be eligible for: Performance related bonus (discretionary and subject to eligibility criteria) BUPA Private medical cover - Immediate cover from day 1 Competitive pension scheme + Life Assurance Generous Annual Leave allowance (increasing with service) plus bank holidays Retailer Discounts Enhanced maternity/paternity and adoption pay Length of Service Awards Christmas Vouchers Health & Wellbeing initiatives An additional day off for your birthday Discounted Gym Membership SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, colour, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law. APPLY NOW for full consideration, if you are selected for an interview, or further consideration, we will be in touch with you directly.

Responsibilities

The role involves reviewing final reports and raw data to ensure accuracy and compliance with GLP and GMP standards. The auditor will manage quality documentation and liaise with clients and study leadership regarding deviations and CAPAs.