Do you have auditing experience or are you already working in a GLP / GCP environment and want to consider Quality Assurance as your next career move? Do you want to be part of a company that helps build a healthier and safer world? Are you looking for industry recognised training and development opportunities? Labcorp is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. As a GLP/GCP Quality Assurance Auditor at Labcorp based in Harrogate, North Yorkshire, you will play an essential part in making this happen. We are looking for someone who is able to apply regulatory knowledge and critically assess data, whilst working in an ever-changing environment. Responsibilities will include: Conducting, but not limited to protocol review, report/data audits and internal facility/process inspections Navigating, reading and understanding specific regulations Being able to answer questions relating to audit findings (successful interaction/relationships on small scale outside QA function) Peer reviewing QA SOPs Supporting Operational liaison meetings representing QA function Making suggestions for improving compliance and/or efficiency of the local QA organization and business units supported Reporting on relevant quality metrics (for single topics/departments) and highlighting trends Ensuring Regulatory Compliance and Quality Assurance (RC&QA) responsibilities, as indicated in applicable controlled documents, are followed What Labcorp can offer you: Competitive salary and a comprehensive benefits package including health cover and contributory pension Unrivalled opportunities to develop a successful career in the scientific industry Unsurpassed career development opportunities A culture of CARE with access to well-being programs and various employee resource groups Education: A minimum of a Bachelor’s Degree in Life Sciences preferred (or equivalent Life Science experience) Experience may be substituted for education Skills / Experience: Auditing experience, preferably to GLP or a proven work history in a regulatory environment working to GLP / GCP Ability to apply relevant regulatory knowledge Ability to follow instruction e.g. QA documents (SOPs) Ability to assimilate/interpret operational documents such that audit can be performed to required level Ability to critically assess data and apply procedures and regulations Ability to challenge processes and make suggestions for improvement Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. A dditionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement .