Quality Control Instrumentation Technician II

Sanofi

Swiftwater (Monroe County)

On-site

USD 28,000 - 47,000

Full time

2 days ago
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Job summary

Sanofi is seeking a Quality Control Technician II in Swiftwater, PA, on site for a 12-month contract. You will support qualification, calibration, PM, and documentation for QC lab instrumentation within a cGMP environment.

Collaborate with QC, Engineering, Validation, QA, Manufacturing, and external vendors to uphold data integrity and regulatory readiness. Ideal candidates have 2+ years in a regulated pharma QC setting, experience with instrument qualification and GMP docs, and strong

Qualifications

  • Minimum 2 years of cGMP-regulated pharma QC laboratory experience.
  • Experience supporting laboratory instrumentation in a regulated environment preferred.
  • Proven ability to author/revise GMP documents (SOPs, protocols, technical assessments).
  • Demonstrated project leadership and improvements experience preferred.

Responsibilities

  • Support qualification, calibration, preventive maintenance, troubleshooting, and retirement of QC instrumentation.
  • Coordinate instrument lifecycle management to keep equipment compliant and reliable.
  • Assist with vendor management and service coordination for lab equipment.
  • Maintain documentation and asset management systems for instrumentation.

Skills

cGMP compliance
Data integrity
Deviations & CAPAs
AIQ/CSV knowledge
Instrument qualification
Preventive maintenance
Lab instrumentation
eQMS experience
Cross-functional collaboration
Technical communication
Troubleshooting
Project leadership
Lab systems (HPLC/GC)
Regulatory compliance
Customer service

Education

Bachelor's degree in Life Sciences or related

Tools

HPLC
GC
Spectroscopy
Dissolution
TOC
Conductivity
Particle counters
Balances
eQMS
CSV validation

Job description

Sanofi is seeking a Quality Control Technician II in Swiftwater, PA, on site for a 12-month contract. You will support qualification, calibration, PM, and documentation for QC lab instrumentation within a cGMP environment.

Collaborate with QC, Engineering, Validation, QA, Manufacturing, and external vendors to uphold data integrity and regulatory readiness. Ideal candidates have 2+ years in a regulated pharma QC setting, experience with instrument qualification and GMP docs, and strong

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