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Revvity

Translational multi-omics and diagnostics provider

Clinical Laboratory Manager

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeHebron, KY, USA$112k - $150k /yrIn-person

About the Job

Requirements

  • A bachelor's degree in Medical Technology, Clinical Laboratory Science, Biology, Biotechnology, or another life science discipline, plus at least 5 years managing laboratory operations in a regulated environment, 10 years working in a laboratory using cellular therapy, cord blood banking, tissue processing, and/or cryopreservation practices, and 10 years of experience with flow cytometry, manual and automated cell counting techniques, blood typing, and molecular laboratory methods; or a master's degree in the same fields, plus at least 3 years managing laboratory operations in a regulated environment, 5 years of relevant laboratory experience, and 5 years of experience with the stated analytical methods.
  • Experience operating and maintaining compliance with FDA regulations, AABB Standards, CLIA, cGTP, and cGMP requirements.
  • Proven ability to lead technical staff, manage laboratory performance, and drive operational excellence.
  • Excellent written and verbal communication skills, with experience developing technical procedures and presenting performance and quality data.

Responsibilities

  • Oversee daily laboratory operations related to cord blood and cord tissue processing, testing, cryopreservation, and release activities.
  • Direct and supervise laboratory technologists, providing leadership, training, performance management, and professional development.
  • Ensure accurate characterization of cellular products using flow cytometry, hemacytometry, blood typing, and molecular testing methodologies.
  • Review and approve laboratory data, test results, batch records, and associated documentation to ensure accuracy, completeness, and regulatory compliance.
  • Provide technical expertise and troubleshooting support for laboratory processes, equipment, assays, and workflow challenges.
  • Lead method validations, process qualifications, and implementation of new technologies and procedures.
  • Develop, revise, and maintain standard operating procedures, work instructions, and technical documentation.
  • Monitor laboratory key performance indicators, operational metrics, and quality indicators to drive continuous improvement initiatives.
  • Investigate deviations, nonconformances, and quality events, and communicate findings and corrective actions to Laboratory Leadership and Quality Management.
  • Partner with Quality Assurance to support audits, inspections, corrective and preventive actions, and regulatory submissions as required.
  • Ensure adherence to applicable laboratory safety, quality, and regulatory standards.

About the Company

Revvity

Translational multi-omics and diagnostics provider

Revvity provides health science solutions that cover the full journey from discovery to development and from diagnosis to cure. Its products span translational multi-omics technologies, biomarker identification, imaging, prediction, screening, detection and diagnosis, and informatics to support pharma, biotech, diagnostic labs, academia and governments. It differentiates itself by offering an end-to-end platform with integrated workflows and specialized support to accelerate development timelines. Its goal is to turn previously impossible healthcare outcomes into achievable ones by advancing discovery, development, diagnosis and patient care.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Waltham, MA
Founded
2023

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