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Closed
Leiden
22 Apr 2026
Equipment Lifecycle Engineer logo

Equipment Lifecycle Engineer

Eurofins

Closed
Leiden
22 Apr 2026
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Equipment Lifecycle Engineer

Equipment Lifecycle Engineer needed at Eurofins BioPharma Product Testing in Leiden, Netherlands. Responsible for planning, scheduling, and performing actions on GxP systems to ensure compliance throughout the equipment lifecycle. Requires a Bachelor's degree in Life Sciences or related field and minimum 1 year experience in a QA/GMP-regulated environment.

On-siteFull-timeEntry LevelGxPMaintenance

Equipment Lifecycle Engineer

Equipment Lifecycle Engineer needed at Eurofins BioPharma Product Testing in Leiden, Netherlands. Responsible for planning, scheduling, and performing actions on GxP systems to ensure compliance throughout the equipment lifecycle. Requires a Bachelor's degree in Life Sciences or related field and minimum 1 year experience in a QA/GMP-regulated environment.

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On-siteFull-timeEntry LevelGxP

Salary

Not specified

Work Location

Leiden, South Holland, Netherlands, NL

Work Model

On-site

Experience Required

1 years

Employment Type

Full-time

Experience Level

Minimum of 1 year of experience in a QA/GMP-regulated environment

Core Qualifications

Technical (Must-have)
GxPMaintenanceCalibrationLife SciencesValidationAnalytical ChemistryGMPMS OfficeData IntegrityQA/GMP
Soft Skills
CollaborationTrainingAdvisingProblem solving

Key Responsibilities

  • •Performing preventive and corrective maintenance on laboratory equipment
  • •Performing calibration work on utilities and laboratory equipment
  • •Performing validation/qualification of laboratory equipment
  • •Performing periodic evaluations and assessments on data integrity
  • •Identifying, reporting and adequately handling malfunctions of utilities, laboratory equipment and facilities
  • •Adequately handling alarms reported via monitoring systems
  • •Training and advising colleagues in the use, maintenance, calibration and validation of utilities and laboratory equipment in accordance with the relevant procedures
  • •Participating in inspections and audits
  • •Management of new equipment (supplier selection, drafting URS), and providing documentation related to this equipment
  • •Initiating and (helping) solving non-conformances, out-of-specifications, changes and complaints, where applicable in collaboration with the QA team
  • •Creation of good system workflows in collaboration with operations departments
Equipment Lifecycle EngineerPharmaceutical ManufacturingEngineeringLife SciencesAnalytical ChemistryQA/GMPValidationMaintenanceCalibrationData Integrity
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