QC Analyst – GMP Lab, Data & Documentation

Roche Holding AG; Tucson (AZ); On-site; USD 49,000 - 92,000; Full time

Job summary

Roche Holding AG in Tucson, AZ is seeking a Quality Control Associate to join our QC team and perform inspection and testing across raw materials, in-process, and finished goods. You will generate and sign off on quality documentation, and maintain lab records in a regulated ISO 13485 and cGMP environment.

The role emphasizes data analysis, accurate reporting, and collaboration with cross-functional teams to support release decisions, investigations, and process improvements.

Qualifications

• High School Diploma with 7 years of experience.
• Associate's Degree with 3 years of experience.
• Bachelor's Degree with 1 year of experience (entry level).
• Excellent oral and written communication skills in a regulated environment.
• Strong data-analysis and problem solving in a GLP/cGMP/ISO setting.
• Hands-on laboratory experience and precise pipetting methods.
• Experience adhering to safety, calibration, and quality procedures.

Responsibilities

• Inspect and test raw materials, in-process materials, and finished goods.
• Document test results, batch records and observations.
• Analyze data and generate QC reports for release.
• Maintain QC lab records and equipment per SOPs.
• Support OOS investigations and CAPA activities.
• Coordinate with cross-functional teams for quality investigations.
• Assist in validations and process improvements.
• Ensure OSHA, FDA, QSR, ISO compliance in daily tasks.

Skills

Data analysis

Communication

Laboratory experience

Pipetting techniques

Attention to detail

Google Suite

Deadline oriented

GMP/GLP/ISO knowledge

Lean/6S

Handling hazardous reagents

Education

High School Diploma

Associate's Degree

Bachelor's Degree

Job description

Roche Holding AG in Tucson, AZ is seeking a Quality Control Associate to join our QC team and perform inspection and testing across raw materials, in-process, and finished goods. You will generate and sign off on quality documentation, and maintain lab records in a regulated ISO 13485 and cGMP environment.

The role emphasizes data analysis, accurate reporting, and collaboration with cross-functional teams to support release decisions, investigations, and process improvements.