QC Specialist: Reagent Manufacturing & Testing

TALENT Software Services; Tucson (AZ); On-site; USD 70,000 - 90,000; Full time

Job summary

Roche Quality Control Associate - Reagent Manufacturing will be integral to a team performing raw material and finished goods testing. You will review, generate and sign off quality documentation, interfacing with complex systems in an ISO 13485 and cGMP environment.

You will maintain records, investigate OOS, and work with guidance from senior staff to ensure compliant processes and timely releases.

Qualifications

• High attention to detail and ability to manage documentation.
• Experience in regulated environments (ISO 13485, cGMP) preferred.
• Strong data-analysis and troubleshooting skills.

Responsibilities

• Inspect and test raw materials, in-process materials and finished goods.
• Document results, complete batch records, and generate QC reports.
• Analyze test results and maintain QC documentation for material releases.
• Ensure lab records and environment comply with regulatory requirements.
• Support in equipment maintenance and analytical method validations.

Skills

Analytical

Problem solving

Great communication

Organization skills

Lifting 25 lbs

Stamina

Education

High School Diploma

Associate or Bachelor in Science

Job description

Roche Quality Control Associate - Reagent Manufacturing will be integral to a team performing raw material and finished goods testing. You will review, generate and sign off quality documentation, interfacing with complex systems in an ISO 13485 and cGMP environment.

You will maintain records, investigate OOS, and work with guidance from senior staff to ensure compliant processes and timely releases.