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Histology LIMS Technical Support

Laboratory Corp of America

Bengaluru IndiaEntry
Sign in to applyVerified 2h ago
Location
Bengaluru India
Work model
On-Site
Level
Entry
Posted
Aug 12, 2026

Skills

GCP

About this role

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives. Labcorp is a global leader in diagnostic testing and drug development solutions, helping healthcare providers, researchers, and patients make informed decisions that advance care. Join us in our mission to improve health and improve lives. Labcorp is seeking a Histology LIMS Technical Support to set up, maintain, and provide quality oversight of pathology studies within laboratory systems. This role is responsible for ensuring study requirements are accurately implemented across operational platforms, supporting study modifications, maintaining documentation, and collaborating with cross-functional teams to ensure compliant and efficient study execution. Work Schedule Remote-based 2:00 PM to 11:00 PM IST 1 Year Fixed-term role with Labcorp Key Responsibilities Perform study setup and maintenance within laboratory systems, including PSI loading and study modifications. Review study documentation (SOWs, PRFs, worksheets, amendments, and related documents) to ensure accurate system configuration. Perform quality control checks on study setups and updates prior to implementation. Maintain study-related documentation, trackers, and records to ensure traceability and compliance. Support the management of study amendments and ensure updates are implemented consistently across systems and operational documents. Collaborate with Histology Technical Liaisons, Project Management, Laboratory Operations, and other stakeholders to resolve study setup issues. Investigate and support resolution of discrepancies related to study setup, documentation, and system configuration. Contribute to process improvement initiatives aimed at enhancing compliance, efficiency, and operational excellence. Ensure adherence to applicable SOPs, work instructions, quality standards, and regulatory requirements. Support audits, inspections, Quality Events, CAPAs, and effectiveness checks as required.

Minimum Qualifications

Bachelor's degree in Life Sciences, Biomedical Sciences, Laboratory Sciences, or a related field. Relevant experience may be considered in lieu of education. 1-3 years of experience in laboratory operations, study setup, project coordination, pathology services, or a related field.

Preferred Qualifications

Experience with pathology or histology workflows. Familiarity with laboratory systems such as Envision, Zavacor, LIMS, or related platforms. Experience managing study amendments, document control, or operational change management processes. Understanding of Good Clinical Practice (GCP), Good Laboratory Practice (GLP), quality systems, or regulated laboratory environments. Additional Requirements Strong organizational skills with the ability to manage multiple studies and priorities simultaneously. Excellent attention to detail and ability to work with process-driven documentation. Strong written and verbal communication skills. Proficiency with Microsoft Office applications and data management tools. Ability to work independently and effectively within a global, cross-functional environment. Strong commitment to quality, accuracy, and compliance. Ability to

Listing verified 2h ago. Applications go through the company's official careers site.

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