QC Instrument Lifecycle Specialist II

eTeam; Swiftwater (Monroe County); Vor Ort; USD 65.000 - 90.000; Vollzeit

Zusammenfassung

eTeam is seeking a Quality Control Instrument Support Specialist II in Swiftwater, PA to manage qualification, calibration, maintenance, and retirement of QC laboratory instruments. You will ensure equipment remains compliant, qualified, and available for operations in a cGMP environment.

Collaborating with QC, Engineering, Validation, QA, Manufacturing, and external service providers, you will maintain instrument documentation, support inspections, and drive continuous improvement initiatives

Qualifikationen

• Bachelor's degree in Life Sciences, Chemistry, Biology, Engineering, Pharmaceutical Sciences, or a related scientific discipline.
• Minimum 2 years of experience in a cGMP-regulated pharmaceutical, biotechnology, medical device, or quality control laboratory environment.

Aufgaben

• Support qualification, calibration, preventive maintenance, troubleshooting, and retirement of QC laboratory instrumentation.
• Ensure activities comply with cGMP, data integrity, site procedures, and regulatory expectations.
• Assist with instrument lifecycle management and vendor coordination.
• Develop and maintain instrument-related documentation and CAPA tracking.
• Lead or participate in projects to improve laboratory efficiency and compliance.

Kenntnisse

cGMP regulations

Data integrity

Quality systems

Instrument qualification

Technical writing

Ausbildung

Bachelor's degree in Life Sciences, Chemistry, Biology, Engineering, Pharmaceutical Sciences, or a related scientific discipline

Minimum 2 years of experience in a cGMP-regulated pharmaceutical, biotechnology, medical device, or quality control laboratory environment

Tools

eQMS

CSV

AIQ

Calibration software

Jobbeschreibung

eTeam is seeking a Quality Control Instrument Support Specialist II in Swiftwater, PA to manage qualification, calibration, maintenance, and retirement of QC laboratory instruments. You will ensure equipment remains compliant, qualified, and available for operations in a cGMP environment.

Collaborating with QC, Engineering, Validation, QA, Manufacturing, and external service providers, you will maintain instrument documentation, support inspections, and drive continuous improvement initiatives