Microbiologist & Sterilization Validation Tech - Onsite

ManpowerGroup; 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 Asset

Supplemental Life Insurance

Short Term Disability Insurance

Long Term Disability Insurance

Travel Insurance

401(k) with Match

Weekly Pay

Job summary

ManpowerGroup seeks a Microbiologist to perform documentation updates in the quality system and conduct EO sterilization validation activities in Temecula, CA, 100% onsite. The role includes investigating dose audit failures and supporting residual EO and D-value studies to ensure product sterility and regulatory compliance.

Ideal candidates hold a Bachelor's degree or equivalent with 0-2 years of related experience and a solid understanding of microbiology and sterilization validation in a

Qualifications

• Bachelor's degree in a related field or equivalent experience.
• 0-2 years of related work experience in microbiology or sterilization.
• Foundational understanding of microbiology and sterilization validation concepts.
• Ability to operate within a quality system and comply with regulatory standards.

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.

Education

Bachelor's degree or equivalent in related field

Job description

ManpowerGroup seeks a Microbiologist to perform documentation updates in the quality system and conduct EO sterilization validation activities in Temecula, CA, 100% onsite. The role includes investigating dose audit failures and supporting residual EO and D-value studies to ensure product sterility and regulatory compliance.

Ideal candidates hold a Bachelor's degree or equivalent with 0-2 years of related experience and a solid understanding of microbiology and sterilization validation in a