Microbiology & EO Sterilization Specialist – Onsite Temecula

ManpowerGroup Global, Inc.; Temecula (CA); On-site; USD 36,000 - 40,000; Full time

Benefits offered by this job

Medical and Prescription Drug Plans

Dental Plan

Vision Plan

Health Savings Account

Health Flexible Spending Account

Dependent Care Flexible Spending Fund

Supplemental Life Insurance

Short Term Disability

Long Term Disability

Business Travel Insurance

401(k) with Match

Weekly Pay

Job summary

ManpowerGroup Global, Inc. is seeking a Microbiologist in Temecula, CA. This 100% onsite role focuses on documentation in the quality system and EO sterilization validations to ensure product sterility and regulatory compliance.

The incumbent will perform EO validation activities, investigate failures, and support related residual studies, following strict procedures while upholding safety standards.

Qualifications

• Bachelor's degree in a related field or equivalent experience.
• 0–2 years of microbiology/sterilization exposure.
• Understanding of quality systems and regulatory standards.
• Ability to follow procedures and maintain safety.

Responsibilities

• Perform documentation updates in the quality system for accuracy and compliance.
• Conduct EO sterilization validation activities, including new product qualification and revalidation.
• Investigate dose audit failures and EO biological indicator sterilization positives.
• Follow procedures and execute tasks per instructions with high quality and safety.
• Support EO residual studies, D-value studies, and related validation activities.

Skills

Sterilization processes

Quality system experience

Documentation skills

Regulatory awareness

Education

Bachelor's Degree or equivalent

Tools

Sterilization validation

Job description

ManpowerGroup Global, Inc. is seeking a Microbiologist in Temecula, CA. This 100% onsite role focuses on documentation in the quality system and EO sterilization validations to ensure product sterility and regulatory compliance.

The incumbent will perform EO validation activities, investigate failures, and support related residual studies, following strict procedures while upholding safety standards.