GMP Equipment Validation Specialist

GMP Equipment Validation Specialist- ICON - Lenexa KS 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. Title: GMP Equipment Validation Specialist Location : Lenexa, KS What you will do : As a GMP Equipment Validation Specialist at ICON you will be responsible for the ongoing qualification of equipment and controlled environments supporting 2 GMP pharmacies and a QC Laboratory. This includes cleanrooms, refrigerators, temperature mapping, IQ/OQ/PQ activities, change controls, audit support, and onboarding new equipment and controlled spaces. The specialist will be based in Lenexa, work closely with the on-site teams, and provide remote support to the GMP pharmacy in San Antonio. The role requires someone who can manage validation activities independently while partnering with Quality, Facilities, Pharmacy, and laboratory stakeholders. Key responsibilities include: Conducting validation and qualification activities for equipment, controlled environments, and related processes used in GMP pharmacy and laboratory operations to ensure compliance with regulatory requirements. Collaborating with cross-functional teams to define validation strategies and documentation standards. Overseeing the execution of validation protocols, including installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ). Supporting temperature-mapping activities for cleanrooms, refrigerators, and other temperature-controlled equipment. Providing technical guidance on equipment validation and qualification methodologies and best practices to enhance operational efficiency. Assisting in the identification and remediation of issues related to equipment qualification, controlled environments, and regulatory compliance. Supporting change-control activities and responding to audits related to validated equipment and facilities. Your Profile: You will bring relevant scientific operations experience, along with the following qualifications and skills. Required qualifications and experience: Bachelor’s degree in a relevant field such as life sciences, engineering, or a related technical discipline. At least one year of GMP equipment validation or qualification experience within the pharmaceutical, laboratory, or clinical research industry, with a solid understanding of applicable regulatory requirements. Experience with IQ/OQ/PQ protocols and validation documentation. Experience with temperature mapping, cleanrooms, controlled environments, or temperature-controlled equipment is preferred. Strong analytical and problem-solving skills with keen attention to detail. Ability to independently manage validation activities and multiple projects while collaborating with cross-functional teams. Excellent communication skills, with the ability to clearly convey technical information to non-technical stakeholders. 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