Sr Auditor, Quality Assurance ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. Onsite: Lenexa, KS Sr Auditor, QA We are currently seeking a Sr Auditor, Quality Assurance to join our diverse and dynamic team. As a Sr Auditor, Quality Assurance at ICON, you will play a pivotal role in providing quality oversight of GMP/CMC activities supporting clinical trials, interpreting applicable regulatory requirements, and ensuring ongoing compliance, while contributing to the advancement of innovative treatments and therapies. What You Will Be Doing: Serving as the Quality Assurance releasing authority for GMP/CMC activities, including review and disposition of applicable GMP documentation and activities prior to release. Providing dedicated Quality Assurance oversight for GMP operations, including manufacturing, pharmacy, QC laboratory, and other CMC-related activities, as applicable. Reviewing and approving GMP records and quality documentation, including batch records, deviations, investigations, CAPAs, change controls, and other applicable GMP documentation. Ensuring GMP/CMC activities are performed in accordance with applicable GMP requirements, internal quality systems, approved procedures, and client requirements. Providing independent QA guidance and decision-making support for GMP quality and compliance matters, including escalation and resolution of issues that may affect product quality or release. Partnering closely with Manufacturing, Pharmacy Services, QC Lab, and CMC teams to provide proactive QA oversight throughout planning and execution, rather than relying solely on retrospective review. Supporting inspection and audit readiness for GMP/CMC operations and driving continuous improvement of the site quality system. Acting as a key Quality representative for GMP/CMC operations and sponsor interactions related to quality, compliance, and release activities. Collaborating with cross-functional teams to identify areas for improvement in quality assurance processes and practices. Developing and implementing audit plans and strategies to assess the effectiveness of quality management systems. Providing expert guidance and recommendations to stakeholders on quality assurance best practices and regulatory requirements. Contributing to the continuous improvement of quality assurance programs and initiatives. Your profile Bachelor's degree in Life Sciences, Pharmacy, or related field; advanced degree preferred. Minimum of 7 years of experience in quality assurance within the pharmaceutical, biotechnology, or CRO industry, with at least 3 years in a leadership role. In-depth knowledge of regulatory requirements and guidelines governing clinical trials (e.g., ICH-GCP, FDA regulations). Strong analytical and problem-solving skills, with the ability to identify and address complex quality issues. Excellent communication and interpersonal skills, with the ability to effectively interact with internal and external stakeholders at all levels. #LI-SB7 #LI-onsite Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here. Are you a current ICON Employee? Please click here to apply ICON is an award-winning workplace that enables you to make a difference to patients’ lives by being part of a world-class clinical research organisation that helps deliver new medicines & medical devices that are benefitting patients worldwide. You are also part of a diverse company that cares about our world and is dedicated to conducting business more sustainably and supporting the communities in which we live. If you’re as driven as we are, join us. You’ll be working in a great environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry. Didn’t find the role you were looking for? Even if the perfect role isn’t available right now, we’re always excited to connect with talented individuals. Register to our Talent Community to receive updates on roles that align with your career goals.

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