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Company Description QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.Log on now to our website. qrcgroup.Com / to learn more about our services and solutions!Job DescriptionThe Laboratory Equipment Validation Specialist is responsible for the validation and lifecycle management of laboratory equipment used in a regulated pharmaceutical environment. This role ensures compliance with cGMP regulations through the planning, execution, and documentation of validation activities for analytical instruments, with a strong focus on UPLC systems and densitometer. The specialist will support laboratory operations by maintaining validated states and ensuring data integrity and regulatoryQualificationsBachelor's degree in Science,
or a related scientific discipline.Minimum of three (3) years of relevant experience in a regulated laboratory in pharmaceutical environment.Demonstrated hands-on experience in the validation of UPLC systems and densitometer.Strong knowledge of equipment qualification and validation requirements, data integrity principles, and applicable regulatory expectations.Bilingual in English and Spanish (written and spoken).Excellent technical writing, organizational, and communication skills.Additional InformationAll your information will be kept confidential according to EEO guidelines.
Postúlate en Kit Empleo: kitempleo.com.co/empleo/1aopbo