Job ref: QAG040226 Job type: Permanent Location: Newry Closing date: Wednesday 18 Feb 2026 12:00 Job Overview The QA GLP Inspector is responsible for conducting inspections and generating audit reports within the R&D GLP Division to ensure compliance with Good Laboratory Practice Guidelines (SI 3106) and OECD GLP standards published as OECD Principles on Good Laboratory Practice (Revised 1997, ENV/MC/CHEM (98)17) and the requirements of Directive 2004/9/EC and 2004/10/EC and associated national legislation. Assist in the upkeep of a current and effective Quality Management System in accordance with Regulatory Authority requirements, company standards and best practices. Essential Criteria: Educated to degree level in a relevant life science related discipline or a minimum of two years' relevant experience working within a GLP or GMP environment. (Full training will be provided). Previous laboratory experience, including reviewing data using Empower (CDS). Experience in maintenance and trending of deviation and laboratory Investigation systems. Experience in managing Change Control. Demonstrate the Ability to read and interpret laboratory procedures, methods and data, GLP and regulatory guidance. Strong attention to detail. Excellent organisation and communication skills (written and verbal) across a range of interdepartmental levels. Demonstrate the ability to work independently on assigned responsibilities as well as part of a team to a high standard to meet deadlines. A full driving licence is required. Desirable Criteria: Experience working in a QA function in a GLP or GMP environment. Experience in the approval, introduction and control of study and facility related documentation. Experience developing and maintenance of Excel spreadsheets for tracking purposes. Understanding of bio-analysis Demonstrable experience in a Clinical setting (in-house and/or CROs etc.,) working on clinical and non-clinical studies operating to GLP Understanding of Good Laboratory Practice principles and standards and quality management systems Knowledge of FDA/EMA practices and guidelines Knowledge of Pharmacovigilance (PV) guidelines and previous experience of conducting PV audits. Experience in the trending and interpretation of analytical data Experience of preparing responses to regulatory queries Duration: Full time, permanent Location: Newry Additional Information: Applicants should have a right to work in the UK at the time of their application (proof required). Benefits: Free Life Assurance Company Pension Scheme Healthcare cash plan 32 days annual leave Wedding Leave Company Sick Pay Employee well-being initiatives Employee Assistance Programme FREE on-site parking Canteen Facilities Employee Perks scheme Annual Employee raffle Employee Recognition scheme Career development To Apply Please forward your CV via the APPLY Now button below.