genscript
Expert - QA Technical Operations
At a Glance
- Location
- Pennington, New Jersey, United States
- Experience
- 5+ years
- Posted
- 2026-03-16T15:51:18-04:00
Key Requirements
Domain Knowledge
- Engineering
- Manufacturing
- Medical
Requirements
3-5+ years of experience in Quality, Manufacturing, Engineering, or related field
GenScript USA Inc/ProBio Inc.
GenScript USA Inc./ProBio Inc.
Please note: Genscript USA Inc./ProBio Inc.
GenScript/Probio does not request personal information from candidates through individual email or any other platform.
Responsibilities
Oversee the GMP supplier qualification program and supplier risk management
Completes the approval requirements to qualify new suppliers including negotiating quality agreements, as well as audit scheduling, conduction of audits, and authoring of audit reports
Periodic review of suppliers and identification of supplier compliance issues
Manages vendor complaints
Participates in or manages quality assessments of internal operations and suppliers to analyze compliance and assess risk
Liaison between Supplier and QA representatives in addressing the quality concerns from the supply chain