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Calibration Technician

Job in New York, New York County, New York, 10261, USA
Listing for: Intellectt Inc
Full Time position
Listed on 2026-02-12
Job specializations:
  • Engineering
    Validation Engineer, Instrumentation Tech, Quality Engineering, Manufacturing Engineer
  • Manufacturing / Production
    Validation Engineer, Instrumentation Tech, Quality Engineering, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 60000 USD Yearly USD 60000.00 YEAR
Job Description & How to Apply Below
Location: New York

The Calibration Technician is responsible for performing calibration, maintenance, and troubleshooting of laboratory, manufacturing, and utility equipment in a GMP-regulated pharmaceutical environment. This role ensures that all critical instruments remain compliant with FDA, cGMP, and internal quality standards to support safe and efficient production operations.

Key Responsibilities
  • Perform calibration, verification, and preventive maintenance of instruments and equipment including:
  • Temperature, pressure, flow, level, pH, conductivity, and analytical instruments
  • Execute calibration activities in accordance with approved SOPs, calibration schedules, and regulatory requirements
  • Troubleshoot out-of-tolerance conditions and document root cause and corrective actions
  • Maintain accurate and compliant calibration records in electronic or paper-based systems (e.g., CMMS, Blue Mountain, SAP)
  • Support audits and inspections (FDA, internal, and third-party) by providing calibration documentation and technical explanations
  • Identify and recommend improvements to calibration processes and procedures
  • Coordinate with Engineering, Maintenance, Validation, Quality Assurance, and Manufacturing teams
  • Ensure compliance with cGMP, FDA, OSHA, and site safety requirements
Required Qualifications
  • Associate’s degree or technical certification in Engineering, Instrumentation, Electronics, or a related field
  • 2+ years of calibration experience in a pharmaceutical, biotech, or GMP-regulated manufacturing environment
  • Strong knowledge of cGMP, FDA regulations, and data integrity requirements
  • Experience calibrating process, utility, and laboratory instruments
  • Ability to read P&IDs, engineering drawings, and equipment manuals
  • Strong documentation and troubleshooting skills
Preferred Qualifications
  • Experience with CMMS systems (Blue Mountain, SAP, Maximo, or similar)
  • Familiarity with USP, ISO, and FDA 21 CFR Part 11 requirements
  • Previous experience supporting equipment qualification or validation activities
  • Strong communication and teamwork skills
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