Sr. Quality Engineer-Metrology

BioPharma Consulting JAD Group; Georgia; On-site; USD 90,000 - 150,000; Full time

Job summary

BioPharma Consulting JAD Group seeks a Senior Quality Engineer with 5+ years in metrology and calibration systems within regulated manufacturing. Lead remediation efforts, perform risk assessments, and drive audit readiness across medical device, pharmaceutical, and biotech environments.

You will work with metrology and calibration equipment, apply MSA and Gage R&R principles, and collaborate with manufacturing, validation, and quality teams to ensure compliance and product quality.

Qualifications

• Bachelor’s degree in Engineering, Quality, Metrology, or related field.
• 5+ years in metrology, calibration, or quality engineering in regulated industries.
• Experience leading calibration program remediation, CAPA execution, and audits.
• Strong knowledge of metrology concepts, MSA, and calibration principles.

Responsibilities

• Lead or support remediation of metrology and calibration programs in regulated industries.
• Conduct gap assessments, identify deficiencies, and develop remediation plans.
• Address audit observations, CAPAs, and regulatory findings for calibration systems.
• Improve calibration compliance, reduce overdue calibrations, strengthen governance.
• Apply metrology knowledge and calibration principles in daily work.
• Support audits and perform risk-based assessments on calibration events.
• Manage projects, timelines, and deliverables across groups.

Skills

Metrology

Calibration systems

Dimensional metrology

MSA (Measurement System Analysis)

Gage R&R

Risk assessment

Audit readiness

CAPA execution

Statistical analysis

Minitab

Education

Bachelor’s degree in Engineering or related technical discipline

Tools

ProCal V5

Siemens Teamcenter

Minitab

Job description

We are seeking a highly experienced Senior Quality Engineer with 5+ years of expertise in metrology and calibration systems within a regulated manufacturing environment. The ideal candidate will be capable of assessing the current state of the calibration program, identifying compliance and technical gaps, performing risk‑based impact assessments, and leading a comprehensive remediation effort that withstands internal audits, customer audits, and regulatory inspections.

Key Responsibilities

• Lead or support remediation of metrology and calibration programs in regulated industries (medical device, pharmaceutical, aerospace, etc.).
• Conduct gap assessments, identify compliance deficiencies, and develop sustainable remediation plans.
• Address audit observations, CAPAs, and regulatory findings related to calibration systems.
• Improve calibration compliance, reduce overdue calibrations, and strengthen calibration governance.
• Apply deep knowledge of dimensional metrology, measurement system analysis, and calibration principles.
• Demonstrate strong understanding of measurement uncertainty, tolerance analysis, traceability, guard banding, and calibration intervals.
• Perform fitness‑for‑use evaluations and apply decision rules (PAR, TMU, Z%, RSS guardbanding).
• Support calibration and troubleshooting of equipment such as:
• Ultrasonic welders
• Pneumatic presses
• Vision systems
• Automated assembly cells
• Injection molding equipment
• Packaging equipment (FFS, band sealers, shuttle sealers)
• CMMs
• Force/torque systems
• Leak and flow instruments
• Environmental monitoring equipment
• Evaluate out‑of‑tolerance (OOT) conditions and determine product/validation impact.
• Ensure compliance with applicable standards and regulations, including:
• ISO 13485
• 21 CFR Part 820 / QMSR
• ISO 17025 principles
• 21 CFR Part 11 (as applicable)
• Gage R&R and MSA methodologies
• Author and revise calibration procedures, deviations, CAPAs, impact assessments, and risk assessments.
• Support internal, customer, and regulatory audits.
• Independently assess calibration events using risk‑based methodologies.
• Conduct OOT/OOC impact assessments and analyze historical calibration data.
• Apply statistical tools (Minitab or equivalent) to evaluate measurement trends and equipment performance.
• Justify disposition decisions using objective evidence and scientific rationale.
• Lead remediation and improvement initiatives across Engineering, Manufacturing, Validation, Laboratory Operations, and Quality.
• Manage project timelines, prioritize activities, and ensure deliverables are met.
• Train personnel, influence stakeholders, and implement lasting improvements to metrology processes and procedures.

Qualifications

• Bachelor’s degree in Engineering, Quality, Metrology, or a related technical discipline.
• 5+ years of experience in metrology, calibration systems, or equipment quality engineering within a regulated industry (medical device, pharmaceutical, biotech, aerospace, or similar).
• Demonstrated experience leading calibration program remediation, including gap assessments, CAPA execution, and audit response.
• Strong technical expertise in dimensional metrology, measurement system analysis (MSA), and calibration principles.
• Advanced understanding of:
• Measurement uncertainty
• Tolerance analysis
• Traceability
• Guard banding
• Calibration intervals
• Fitness‑for‑use decision rules (PAR, TMU, Z%, RSS)
• Hands‑on experience with a wide range of manufacturing and inspection equipment, including:
• Ultrasonic welders
• Pneumatic presses
• Vision systems
• Automated assembly cells
• Injection molding equipment
• Packaging equipment (FFS, band sealers, shuttle sealers)
• CMMs
• Force/torque systems
• Leak and flow instruments
• Environmental monitoring equipment
• Strong knowledge of quality system regulations and standards, including:
• ISO 13485
• 21 CFR Part 820 / QMSR
• ISO 17025 principles
• 21 CFR Part 11 (as applicable)
• Gage R&R and MSA methodologies
• Proven ability to author and revise calibration procedures, deviations, CAPAs, impact assessments, and risk assessments.
• Experience supporting internal, customer, and regulatory audits.
• Strong analytical and statistical skills; proficiency with Minitab or equivalent tools.
• Demonstrated ability to perform OOT/OOC impact assessments and data‑driven decision making.
• Strong project management skills with the ability to lead remediation efforts, prioritize tasks, and meet aggressive timelines.

Preferred Qualifications

• Experience working in medical device metrology programs.
• Familiarity with cleanroom environments and standards:
• ISO 9001
• ISO 13485
• ISO 17025
• ISO 10012
• ANSI/NCSL Z540
• Working knowledge of:
• ProCal V5
• Siemens Teamcenter

• Shift: Administrative
• Contract Duration: 12 months
• Location: Onsite