Metrology Engineer II

Kindeva Drug DeliveryBridgeton, MO

About The Position

The Senior Metrology Engineer 2 leads advanced metrology, calibration, and measurement-system activities supporting pharmaceutical CDMO manufacturing and laboratory operations. The role ensures measurement integrity, cGMP and data-integrity compliance, program reliability, and continuous improvement while providing technical leadership and cross-functional support.

Requirements

  • Bachelor’s degree in Metrology, Engineering, Physics, Chemistry, or a related technical field; master’s degree preferred.
  • 4+ years of progressive metrology, calibration, or measurement-science experience in a regulated cGMP environment, including laboratory instruments.
  • Strong knowledge of calibration principles, measurement uncertainty, and traceability to national or international standards.
  • Hands-on experience calibrating process instrumentation and pharmaceutical laboratory equipment.
  • Experience with calibration-management systems, CMMS/EAM platforms, and 21 CFR Part 11 data-integrity requirements.
  • Working knowledge of cGMP, quality systems, deviations, CAPA, and change control.
  • Ability to produce clear technical procedures, protocols, and investigation reports.
  • Strong analytical, root-cause, communication, collaboration, prioritization, and technical-leadership skills.

Nice To Haves

  • Experience in aseptic fill-finish, sterile manufacturing, or CDMO operations and supporting laboratories.
  • Familiarity with cleanroom, isolator, utility, and environmental-monitoring instrumentation.
  • Experience with risk-based calibration intervals, measurement system analysis, reliability engineering, or predictive maintenance.
  • ASQ CCT, CQE, or an equivalent professional credential.
  • Experience with equipment introduction, technology or method transfer, or multi-site program standardization.

Responsibilities

  • Lead and improve site or multi-site metrology and calibration programs, including asset lifecycle management, interval optimization, and risk-based practices.
  • Perform and oversee calibrations, qualifications, and measurement system analyses for critical process, utility, and laboratory instruments.
  • Develop, review, and approve calibration procedures, protocols, work instructions, and technical records in accordance with cGMP and internal quality systems.
  • Investigate out-of-tolerance conditions, failures, and deviations; conduct impact assessments and root-cause analyses; and support CAPA effectiveness.
  • Lead the selection, installation, qualification, and integration of new measurement and laboratory equipment, including support for transfers and start-ups.
  • Partner with Engineering, Quality, Validation, Laboratory Operations, Manufacturing, and Maintenance to improve measurement capability and equipment reliability.
  • Maintain calibration-system and CMMS/EAM data, schedules, history, KPIs, and data-integrity controls.
  • Mentor engineers and technicians, review technical work, and support training and competency development.
  • Support regulatory and customer audits with technical expertise, documentation, and responses.
  • Drive improvements in measurement uncertainty, calibration intervals, automation, standardization, business continuity, and reliability.
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