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Laboratory Manager

  • Laboratory Manager job type Posted on: Nov 03, 2026
  • Laboratory Manager experience level GForce Life Sciences
  • Laboratory Manager employment type Chicago, Illinois
  • Laboratory Manager employment type Onsite
  • Laboratory Manager salary Full-time

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Job Title :

Laboratory Manager

Job Type :

Full-Time

Job Location :

Chicago Illinois United States

Remote :

No

Jobcon Logo Job Description :

Laboratory ManagerOur combination-device client seeks a hands-on Laboratory Manager to oversee laboratory operations, staff, equipment readiness, and drug-device combination-product testing. Partner with Engineering, Quality, and Operations to maintain compliance, improve capacity and throughput, and meet client commitments.ResponsibilitiesManage daily priorities, staffing, training, sample flow, testing readiness, documentation, and delivery risks.Lead test method development, optimization, validation/verification, troubleshooting, and failure investigations for autoinjectors, pen injectors, prefilled syringes, and on-body injectors.Oversee functional and dimensional testing, including force/torque, dose accuracy, delivered volume, injection/delivery time, needle performance, adhesion, leakage, alarms, and fault handling.Direct fixture development, equipment selection, and repeatability/reproducibility studies.Own equipment qualification, calibration, maintenance, repairs, and documentation; maintain materials and inventory controls, including receiving, storage, traceability, expiration, and disposition.Partner with Quality on protocols, reports, deviations, nonconformances, CAPAs, change controls, and audit readiness.Required QualificationsBachelor’s in Engineering, Chemistry, Biology, Materials Science, or a related technical field; equivalent relevant experience may be considered.5+ years of laboratory, engineering, manufacturing, or technical operations experience in a regulated or quality-driven environment, including 2+ years of people leadership.Direct experience with test methods, protocols, validation/verification, troubleshooting, and testing requirements for autoinjectors, pen injectors, prefilled syringes, and on-body injectors.Working knowledge of cGMP, ISO 13485, ISO 17025, or comparable requirements and documentation practices.Experience with laboratory operations, equipment qualification, calibration, maintenance, and quality investigations, CAPAs, audits, or out-of-tolerance events.Preferred QualificationsConsulting, contract-development, testing, or service-based organization experience.Materials management, inventory, receiving, traceability, stockroom, or warehouse experience.Knowledge of ISO 11608, ISO 11040, ISO 14971, IEC 62366, and relevant USP chapters.Experience with fixtures, equipment selection, repeatability/reproducibility studies, Lean, 5S, or visual management.Proficiency with Excel and inventory, maintenance, ERP, QMS, or scheduling systems.Term & StartPermanent positionFull-time, 40 hours/weekOnsite in Illinois 4+ days/weekImmediate start

Jobcon Logo Position Details

Posted:

Nov 03, 2026

Reference Number:

10440_4486418499

Employment:

Full-time

City:

Chicago

Job Origin:

APPCAST_CPC

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Laboratory ManagerOur combination-device client seeks a hands-on Laboratory Manager to oversee laboratory operations, staff, equipment readiness, and drug-device combination-product testing. Partner with Engineering, Quality, and Operations to maintain compliance, improve capacity and throughput, and meet client commitments.ResponsibilitiesManage daily priorities, staffing, training, sample flow, testing readiness, documentation, and delivery risks.Lead test method development, optimization, validation/verification, troubleshooting, and failure investigations for autoinjectors, pen injectors, prefilled syringes, and on-body injectors.Oversee functional and dimensional testing, including force/torque, dose accuracy, delivered volume, injection/delivery time, needle performance, adhesion, leakage, alarms, and fault handling.Direct fixture development, equipment selection, and repeatability/reproducibility studies.Own equipment qualification, calibration, maintenance, repairs, and documentation; maintain materials and inventory controls, including receiving, storage, traceability, expiration, and disposition.Partner with Quality on protocols, reports, deviations, nonconformances, CAPAs, change controls, and audit readiness.Required QualificationsBachelor’s in Engineering, Chemistry, Biology, Materials Science, or a related technical field; equivalent relevant experience may be considered.5+ years of laboratory, engineering, manufacturing, or technical operations experience in a regulated or quality-driven environment, including 2+ years of people leadership.Direct experience with test methods, protocols, validation/verification, troubleshooting, and testing requirements for autoinjectors, pen injectors, prefilled syringes, and on-body injectors.Working knowledge of cGMP, ISO 13485, ISO 17025, or comparable requirements and documentation practices.Experience with laboratory operations, equipment qualification, calibration, maintenance, and quality investigations, CAPAs, audits, or out-of-tolerance events.Preferred QualificationsConsulting, contract-development, testing, or service-based organization experience.Materials management, inventory, receiving, traceability, stockroom, or warehouse experience.Knowledge of ISO 11608, ISO 11040, ISO 14971, IEC 62366, and relevant USP chapters.Experience with fixtures, equipment selection, repeatability/reproducibility studies, Lean, 5S, or visual management.Proficiency with Excel and inventory, maintenance, ERP, QMS, or scheduling systems.Term & StartPermanent positionFull-time, 40 hours/weekOnsite in Illinois 4+ days/weekImmediate start

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