QA Auditor I- Labs
About the role
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- Be knowledgeable with all relevant ICON SOPs, ISO 9000 requirements and with appropriate regulations and guidelines.
- Effectively plan and conduct regular and random QA audits (internal and external) in order to assure that clinical studies managed by ICON are of the highest standard and are in compliance with the requirements of ICON or Sponsor SOPs, study protocols, relevant regulations and guidelines and with ISO 9000 requirements.
- Perform quality system audits and perform contract audits for Sponsor as required.
- Ensure that audit results are formally recorded and reported and that corrective/preventive actions are documented.
- When appointed lead auditor, perform the duties assigned in an efficient and effective manner. This includes liaison with the project manager on all QA issues, including audit planning and review of audit results.
- Assist with the development of the project audit procedures.
- Assist in training new QA auditors and provide a benchmark of auditing competencies to inexperienced colleagues.
- Assist in training ICON staff regarding GCP, ISO 9000, role of QA regulatory inspections, etc.
- Conduct induction/orientation of new staff in ICON quality policies and procedures.
- Assist with business development activities (such as marketing presentations) when appropriate.
- Keep the person whom the QA Auditor reports to informed of any QA issues within the department that require attention.
- BS degree in the sciences or related field or local equivalent.
- Adequate experience as determined by QA Management may substitute for that requirement.
- Prior experience (a minimum of one year experience) in medicine, science or other relevant disciplines.
- Previous experience in a GXP quality assurance and/or research environment.
- Ability to review and evaluate data / records. Good oral and written communication skills.
- Ability to liaise successfully with project teams.
- Competent computer skills.
- Proficiency in basic Microsoft Office Suite, including Excel, Word and PowerPoint.
- Additional experience in Document Management System/Data Management systems preferred but not required.
A better career. A better world. A better you.
Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more
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