Microbiologist - EO Sterilization & Validation Onsite

Experis; Temecula (CA); On-site; USD 36,000 - 40,000; Full time

Benefits offered by this job

Weekly Pay

Medical Plans

Vision Plan

Health Savings Account

Flexible Spending Account

Life Insurance

Disability Insurance

Business Travel Insurance

Job summary

Experis in Temecula, CA is seeking a Microbiologist to perform documentation updates in the quality system and conduct sterilization validation activities for ethylene oxide sterilized products. The role includes responding to dose audit failures and EO biological indicator results, following procedures, and supporting related validation studies to ensure sterility and compliance.

The position requires a Bachelor's degree or equivalent with 0-2 years of related experience and a foundational

Qualifications

• Bachelor's degree or equivalent combination of education and work experience.
• 0-2 years of related work experience with foundational understanding of microbiology or sterilization processes.
• Basic technical knowledge of concepts, practices, and procedures relevant to microbiology and sterilization validation.

Responsibilities

• Perform documentation updates in the quality system to ensure accuracy and compliance.
• Conduct sterilization validation activities for ethylene oxide sterilized products, including new product qualification and revalidations.
• Investigate dose audit failures and ethylene oxide biological indicator sterilization positives.
• Follow procedures and execute tasks according to instructions, maintaining high standards of quality and safety.
• Support residual EO studies, D-value studies, and other related validation activities to ensure product sterility and compliance.

Skills

Microbiology basics

Sterilization knowledge

Quality system

Education

Bachelor's degree in related field

Job description

Experis in Temecula, CA is seeking a Microbiologist to perform documentation updates in the quality system and conduct sterilization validation activities for ethylene oxide sterilized products. The role includes responding to dose audit failures and EO biological indicator results, following procedures, and supporting related validation studies to ensure sterility and compliance.

The position requires a Bachelor's degree or equivalent with 0-2 years of related experience and a foundational