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Qa auditor - glp

Huntingdon
Auditor
Posted: 9h ago
Offer description

Are you a skilled and experienced GLP Quality Assurance Auditor looking for a new role offering career development? Do you want to join a company that understands flexible working? Are you committed to supporting process improvement and change? Labcorp is a leading global life sciences company. With a mission to improve health and improve lives, Labcorp delivers world-class diagnostic solutions, brings innovative medicines to patients faster and uses technology to improve the delivery of care. As an experienced Good Laboratory (GLP) Quality Assurance Auditor at Labcorp, based at Huntingdon in Cambridgeshire, you will play an essential part in making this happen. The job will involve: - Conduct, but not limited to protocol review, report/data audits, and internal facility/process inspections - Peer review QA SOPs - Support operational liaison meetings representing QA function - Report on relevant quality metrics (for single topics/departments) and highlight trends - Ensure Regulatory Compliance and Quality Assurance responsibilities, as indicated in applicable controlled documents, are followed - Other duties as assigned by management What Labcorp can offer you: - Competitive salaries and a comprehensive benefits package including health cover and contributory pension - Flexible and remote work once the training has been completed - Unrivalled opportunities to develop a successful career in the scientific industry, QA specialist roles, management training and senior apprenticeships - Unsurpassed career development opportunities and the chance to progress quickly up the career development framework - A culture of CARE with access to well-being programs and various employee resource groups - Subsidised on-site canteen/ restaurant, Gym facilities (small monthly cost) and free parking Experience: - A proven work history in a regulatory environment and experience in GLP QA Auditor roles - Experienced in inspecting and auditing animal Toxicology, Safety Assessment or Pharmacology studies and processes is desired, but not necessary - Experienced using data collection systems such as Pristima and Veeva, but not necessary - Knowledge of the UK and OECD GLP quality systems/standards and able to apply regulations in order to monitor compliance - Experienced in process improvement - Clear communication skills, including ability to provide clear feedback - Able to clearly articulate processes in order to provide training - Able to influence process improvement initiatives / offer solutions 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. Additionally, 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 (https://careers.labcorp.com/global/en/accessibility) or contact us at Labcorp Accessibility. (Disability_apply@LabCorp.com) For more information about how we collect and store your personal data, please see our Privacy Statement (https://www.labcorp.com/about/web-privacy-policy) .

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