Quality Inspector - 2nd Shift, Critical Pharma QA

Thisiscny; Town of Skaneateles (NY); On-site; USD 45,000 - 62,000; Full time

Job summary

Baxter is seeking a Quality Inspector for the 2nd shift to help ensure product quality, safety, and regulatory compliance across the manufacturing process. You will review DHRs, inspect devices and labels, and release products in SAP while maintaining strict adherence to cGMP and FDA requirements.

You should bring a high school diploma with 2–4 years of related experience, familiarity with GMP documentation, and the ability to work flexible hours.

Qualifications

• High School diploma with 2-4 years related experience.
• Experience in a pharmaceutical or Biotech industry helpful.
• Must be familiar with cGMP and FDA requirements.
• Knowledge of aseptic techniques preferred.
• Knowledge of GMP documentation and FDA required.
• Demonstrated attention to details and accuracy required.
• May be required to work flexible hours and overtime on short notice.

Responsibilities

• Perform the inspection of DHR documentation for devices and modules to ensure test procedures are completed and release specs are met.
• Perform internal inspection of devices for visual conformity before release.
• Verify customer facing device and packing labels match serial numbers.
• Approve release of devices in ERP systems and ensure no open nonconformances.
• Record and disposition nonconformances using minor correction workflow and NCR systems.
• Ensure process control and maintenance procedures are followed.
• Assist with identification and containment of nonconforming product on the floor.

Skills

Quality inspection

cGMP knowledge

FDA requirements

Attention to detail

Education

High School diploma

Job description

Baxter is seeking a Quality Inspector for the 2nd shift to help ensure product quality, safety, and regulatory compliance across the manufacturing process. You will review DHRs, inspect devices and labels, and release products in SAP while maintaining strict adherence to cGMP and FDA requirements.

You should bring a high school diploma with 2–4 years of related experience, familiarity with GMP documentation, and the ability to work flexible hours.