Validation Technician: Data & Testing Support

Grifols; Los Angeles (CA); On-site; USD 32,000 - 45,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) match

Paid time off

Job summary

Grifols in California is seeking a Validation Technician to support validation engineers through testing, protocol execution, and data analysis. The role includes calibrations of thermal monitoring equipment, maintaining calibration status, and generating reports.

Responsibilities cover sample collection, protocol documentation, and ensuring cross-department paperwork is complete. Strong attention to detail and English proficiency are required for this FDA-regulated environment.

Qualifications

• Associate degree or equivalent in a technical or scientific discipline.
• Experience in an FDA regulated manufacturing facility preferred.
• English reading/writing/speaking required.
• Ability to work independently with minimal supervision.

Responsibilities

• Support validation engineers through testing, protocol execution, and data analysis.
• Perform pre and post calibrations of thermal monitoring equipment and generate reports.
• Maintain calibration state of thermal mapping equipment and monitor battery life of wireless loggers.
• Collect samples during cleaning, testing and validation and submit to QC.
• Document protocols and ensure paperwork from other departments is available.

Skills

English proficiency

Self-starter

Attention to detail

Documentation & record keeping

Problem solving

Education

Associate degree or equivalent

Tools

Excel

Word

Job description

Grifols in California is seeking a Validation Technician to support validation engineers through testing, protocol execution, and data analysis. The role includes calibrations of thermal monitoring equipment, maintaining calibration status, and generating reports.

Responsibilities cover sample collection, protocol documentation, and ensuring cross-department paperwork is complete. Strong attention to detail and English proficiency are required for this FDA-regulated environment.