• Dallas, TX
  • Quick Apply
4 days ago

Job Description

Responsibilities:
  • Develop and execute Installation, Operational, and Performance Qualification (IQ/OQ/PQ) protocols specifically for blood glucose monitoring sensor manufacturing equipment.
  • Define and document critical process parameters (CPPs) and equipment capabilities to ensure stable sensor performance within specification limits.
  • Establish preventive maintenance plans, calibration schedules, and critical spare parts lists.
  • Author validation plans, validation protocols, test reports, including deviations and corrective actions and Standard Operating Procedures (SOPs).
  • Utilize tools such as Minitab to analyze large datasets from sensor builds, performing Design of Experiments (DOE) and process capability studies.
  • Perform equipment risk assessments, including pFMEA and hazard analysis.
  • Define User Requirements Specifications (URS) for new equipment and lead equipment installation and commissioning efforts.
  • Train technicians and operators on validated equipment procedures.
  • Ensure compliance with FDA 21 CFR Part 820, ISO 13485, and GMP regulations.
  • Partner with R&D, Quality Assurance, and external vendors to scale up pilot lines to high volume production.
  • Work with Manufacturing Engineers to improve equipment reliability and throughput.
  • Support internal and external audits by providing equipment validation evidence.
Requirements:
  • Bachelor's degree in mechanical, Electrical, Industrial, Biomedical Engineering, or a related field.
  • 3+ years of equipment validation experience within medical device manufacturing.
  • Strong understanding of GMP, GAMP 5, and FDA equipment validation requirements.
  • Familiarity with automated equipment, robotics, PLCs, and machine vision systems.
Preferred Qualifications:
  • Prior experience validating equipment for biosensor or electrochemical sensor manufacturing, or experience in the semiconductor industry for wafer production.
  • Experience with high speed automation and semi automated production lines.
  • Certification in equipment validation or GAMP 5 training.

Numbers & Facts

LocationDallas, TX

Skills

  • Analysis Skillsunmatched
  • Automationunmatched
  • Biomedical Engineeringunmatched
  • Calendar Managementunmatched
  • Calibrationunmatched
  • Code of Federal Regulationsunmatched
  • Commissioningunmatched
  • Corrective Actionunmatched
  • Data Setsunmatched
  • Electricityunmatched
  • Electrochemistryunmatched
  • Equipment Validationunmatched
  • Experiment Designunmatched
  • External Auditunmatched
  • FDA (Food and Drug Administration)unmatched
  • FDA Requirementsunmatched
  • GMP (Good Manufacturing Practices)unmatched
  • Hazard Analysisunmatched
  • ISO (International Organization for Standardization)unmatched
  • Industrial Engineeringunmatched
  • Internal Auditunmatched
  • Maintain Complianceunmatched
  • Manufacturingunmatched
  • Manufacturing Engineeringunmatched
  • Manufacturing Equipmentunmatched
  • Medical Equipmentunmatched
  • Minitabunmatched
  • Preventative Maintenanceunmatched
  • Process Capabilityunmatched
  • Process Failure Mode and Effects Analysis (PFMEA)unmatched
  • Process Validationunmatched
  • Production Volumeunmatched
  • Programmable Logic Controller (PLC)unmatched
  • Quality Assuranceunmatched
  • Regulationsunmatched
  • Reliability Engineeringunmatched
  • Requirements Managementunmatched
  • Research & Development (R&D)unmatched
  • Risk Analysisunmatched
  • Roboticsunmatched
  • Semiconductorsunmatched
  • Standard Operating Procedures (SOP)unmatched
  • United States Department of Energy (DOE)unmatched
  • Validation Planunmatched
  • Validation Testingunmatched
  • Wafer Manufacturingunmatched
  • Writing Skillsunmatched

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