Clinical Auditing Specialist III

  • Athlone
  • Thermo Fisher Scientific
:Perform risk based review of highly complex validated systemsLead directed site audits, facility, vendor, and/or sub-contractor auditsProvide GxP consultation and support to project teams and external clientsLead process audits and may participate as a co-auditor in more complex system auditsPerform other types of QA audits or activities such as internal audits, non-conformance review and investigation review.Serve as a resource to operational departments on audit or quality assurance subject matterPrepare and present audit findings and related information at departmental, internal operations, or client meetingsAttend site as required in order to perform client audits, regulatory inspections, internal audits and other activities as requiredProvide mentorship and guidance to junior auditorsRequirements:Bachelor's degree in a related fieldMinimum of 5 years of experience in clinical auditing or quality assuranceStrong knowledge of GxP regulations and guidelinesExceptional attention to detail and ability to ensure flawless execution of auditsProven ability to successfully implement audit processes and proceduresExcellent communication and presentation skillsOur Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.