Calibration Coordinator

Burke Porter, an Ascential Technologies Brand•Andover, MN

2d•Onsite

About The Position

The Calibration Coordinator is responsible for administering and maintaining the calibration program that ensures compliance with U.S. FDA regulations (21 CFR Parts 210/211 and 21 CFR Part 820) as well as international regulatory requirements and industry standards. This role supports product quality, data integrity, and inspection readiness across multiple regulatory jurisdictions, ensuring all instruments and systems are calibrated, documented, and controlled in accordance with global GMP and quality system expectations.

Requirements

High School Diploma or AA Degree at minimum with applicable work experience
3–7+ years of calibration, metrology, or maintenance experience in a regulated pharmaceutical, biotech, or medical device environment
Direct experience supporting global regulatory frameworks and audits
Strong knowledge of cGMP and global GMP frameworks (FDA, EU, WHO)
Strong knowledge of calibration principles and metrology best practices
Strong knowledge of ISO/IEC 17025 laboratory requirements
Familiarity with CMMS systems (e.g., Master Control, ETQ, SAP PM)
Familiarity with data integrity principles and electronic systems compliance (Part 11, Annex 11)
Familiarity with working knowledge of risk management tools and statistical analysis
Strong organizational and coordination skills across multiple stakeholders
High attention to detail and compliance mindset
Ability to communicate effectively in a cross-functional environment
Strong analytical and problem-solving capabilities
Global regulatory expertise
Inspection readiness and audit support
Data integrity and compliance
Risk-based decision making
Cross-functional collaboration
Continuous improvement mindset

Nice To Haves

Bachelor’s degree in Engineering, Life Sciences, Metrology, or related technical discipline preferred

Responsibilities

Coordinate and manage the calibration program for manufacturing, laboratory, and facility equipment.
Maintain calibration schedules aligned with regulatory requirements and risk-based methodologies.
Track and report key performance indicators (KPIs) (e.g., completion rates, overdue calibrations, OOT trends).
Ensure compliance with applicable regulations and standards, including but not limited to: U.S. FDA (21 CFR Part 210/211, 21 CFR Part 820), European Union (EU GMP, EU MDR, IVDR), International Standards (ISO 13485, ISO 9001, ISO/IEC 17025), ICH Guidelines (ICH Q7, Q8, Q9, Q10), and other regulatory bodies (MHRA, Health Canada, TGA, PMDA).
Ensure alignment with data integrity guidance (FDA, MHRA, PIC/S).
Maintain continuous inspection readiness for global regulatory inspections and customer audits.
Maintain calibration records, certificates, and traceability per ALCOA+ principles.
Ensure calibration standards are traceable to NIST, SI units, or equivalent international standards.
Manage calibration data within CMMS and/or validated systems in compliance with 21 CFR Part 11 and Annex 11.
Review calibration documentation for technical accuracy and regulatory compliance.
Lead or support investigations for calibration failures and out-of-tolerance conditions.
Conduct product impact assessments using risk-based methodologies (ICH Q9).
Collaborate on CAPA activities to ensure effective root cause resolution and compliance.
Support deviation, change control, and nonconformance processes.
Coordinate external calibration service providers and laboratories.
Ensure vendors are qualified per ISO/IEC 17025 accreditation and internal supplier quality requirements.
Review vendor documentation and audit performance where required.
Partner with Engineering, Manufacturing, Quality, Validation, and Regulatory Affairs teams.
Support equipment qualification (IQ/OQ/PQ) and lifecycle management.
Provide calibration input into risk assessments, URS, and validation protocols.
Drive improvements in calibration processes using Lean, Six Sigma, or operational excellence tools.
Implement digital solutions and system upgrades (e.g., CMMS, calibration management software).
Perform duties following NACS, Inc. quality and safety standards.
Participate in team building, training, and department communications.
Understand and follow all attendance related policies.
Maintain a high level of personal and professional integrity.
Perform additional job responsibilities as assigned.