Description ABOUT YOU As a QC Auditor / Senior QC Auditor, you will have a strong eye for detail and enjoy working with data, numbers and processes. You will be comfortable reviewing information for accuracy and consistency and following defined procedures within a regulated environment. You will bring a structured and organised approach, with the ability to manage your workload effectively while maintaining a high level of accuracy. You will enjoy working as part of a team, supporting laboratory operations and working closely with scientists to ensure data integrity and quality standards are consistently met. This role would suit: A recent graduate or early career candidate with strong numerical skills Or someone with experience in QC, data review or a regulated environment Required skills and experience: Strong numeracy skills with the ability to check and calculate data accurately High attention to detail and accuracy Good IT literacy skills Clear written and verbal communication skills Ability to follow processes and procedures consistently Ability to manage workload and prioritise tasks Desirable: Scientific background (Biology, Chemistry or related discipline) Experience within a GxP regulated environment (GLP, GMP, GCP) Exposure to data integrity, QC or auditing activities ABOUT THE OPPORTUNITY As a QC Auditor / Senior QC Auditor, you will play a key role in ensuring the accuracy and integrity of laboratory data. You will support laboratory teams by reviewing data, checking calculations and ensuring that all documentation is accurate, consistent and compliant before reporting. This is not a lab-based role. Instead, you will focus on data review and quality control, acting as a key checkpoint between laboratory output and final reporting. This is an excellent opportunity to develop a career in quality, data integrity and regulatory compliance within a highly regulated laboratory environment. Key activities: Reviewing laboratory data, calculations and analytical write-ups for accuracy Verifying that results are correctly calculated and transcribed Reviewing documentation for completeness, consistency and compliance Applying data integrity principles (ALCOA) to all work Identifying and escalating discrepancies or anomalies Working with laboratory teams to resolve data queries Supporting the delivery of accurate reports in a timely manner Ensuring processes and procedures are followed consistently Supporting continuous improvement of data quality and documentation WHAT WE OFFER Join Intertek and become part of our global network of inspiring and entrepreneurial colleagues. We are a global family that values diversity and we thrive working together with precision, pace, and passion. We are working to make the world Ever Better, ensuring the quality, safety and sustainability of products and services used by millions of people around the world. Competitive salary/benefits Development and career opportunities around the Globe Client-facing technical work within a highly motivated team and dynamic working environment We are an Equal Opportunity Employer who do not discriminate against applicants. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex or national origin. Intertek operates a preferred supplier arrangement, and we do not accept unsolicited approaches from agencies