GLP Quality Assurance Auditor - Experienced

<h2>Job Overview:</h2><p style="margin: 0px;"><strong><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Are you a skilled and experienced GLP Auditor looking for career development?</span></strong></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><strong><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Are you committed to driving change and process improvements?</span></strong></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><strong><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Do you want to join a global pharmaceutical company offering huge opportunities for professional development?</span></strong></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">As one of the world’s premier Contract Research Organisations, we provide research services for a multitude of organisations. </span><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">We strive to make a difference to people’s everyday lives by bringing essential products to the market. </span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">As an experienced <strong>Good Laboratory Practice (GLP) Quality Assurance Auditor</strong> at Covance by Labcorp, based at Harrogate in North Yorkshire, you will play an essential part in making this happen.</span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><strong><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">The job will involve:</span></strong></p><p style="margin: 0px;"> </p><ul><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Conducting work as identified on the audit activity table.</span></li><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Reporting on relevant quality metrics (for multiple topics/departments) and highlight trends.</span></li><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Providing consultation to the operational team.</span></li><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Delivery of training in performance of audits (basic, intermediate audit activities).</span></li><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Working with operational management to support Quality topics and/or working on projects with QA team on other sites.</span></li><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Contributing to local Quality initiatives aimed at improving compliance and/or efficiency of the local QA organisation.</span></li><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Author QA SOP's.</span></li><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Ensuring Regulatory Compliance and Quality Assurance (RC&QA) responsibilities, as indicated in applicable controlled documents, are followed.</span></li></ul><p style="margin: 0px;"> </p><p style="margin-bottom: 0.0001pt; text-align: justify;"><strong><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">What Covance by Labcorp can offer you:</span></strong></p><p style="margin-bottom: 0.0001pt; text-align: justify;"> </p><ul style="text-align: justify;"><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Competitive salaries and a comprehensive benefits package including health cover and contributory pension.</span></li><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Unrivalled opportunities to develop a successful career in the scientific industry.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Unsurpassed career development opportunities.</span></li></ul><h2>Education/Qualifications:</h2><ul><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">A minimum of a Bachelor’s Degree in Life Sciences preferred (or equivalent Life Science experience).</span></li><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Experience may be substituted for education.</span></li></ul><h2>Experience:</h2><ul><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">A proven work history in a regulatory environment (experience in GxP roles).</span></li><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Knowledge of industry quality systems/standards and able to apply regulations in order to monitor compliance.</span></li><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Experienced in process improvement.</span></li><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Clear communication skills, including ability to provide clear feedback.</span></li><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Able to clearly articulate processes in order to provide training.</span></li><li style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Able to influence process improvement initiatives / offer solutions.</span></li></ul>