QC Micro EM Analyst - VIVOS Professional Services, LLC : Job Details

Job Title: QC Micro EM Analyst I

Location: Vacaville, CA

Pay Rate: $20.00 – $32.04/hr (W2)

Shift Hours: 6:00 AM – 2:30 PM

Shift Days: Monday – Friday (100% onsite)

Job Summary

The QC Micro EM Analyst I will perform a broad variety of basic and moderately complex tests in support of GMP laboratory operations. Responsibilities include sampling of utility systems and manufacturing process spaces, conducting chemical and microbiological analyses, and supporting continuous improvement initiatives to ensure regulatory compliance, patient supply, and cost-effectiveness.

Key Responsibilities

• Perform routine and non-routine sample testing and accurately document results per GMP requirements
• Conduct sampling of utility systems and manufacturing process spaces
• Perform routine laboratory maintenance and ensure compliance with GMP standards
• Prepare both basic and complex reagents as needed
• Understand theory of assays; mentor others in assay and laboratory functions
• Identify and troubleshoot technical issues; escalate when necessary
• Maintain and order laboratory supply inventory
• Coordinate with customers to support operational activities
• Participate in group and project teamwork, contributing to continuous improvement efforts
• Resolve issues independently where possible, with management approval as required
• Follow all GMP rules and maintain accurate documentation
• Meet scheduled performance targets of 95% on-time testing
• Support Quality by completing tasks assigned by supervisor or manager

Key Requirements

• BS/BA in Biological Sciences, Physical Sciences, or Engineering preferred
• 0–3 years of relevant laboratory experience (GMP environment preferred)
• Knowledge of scientific theories, principles, and techniques used in analytical or microbiological testing
• Strong verbal and written communication skills; ability to organize and present information clearly
• Ability to work under moderate supervision and set short-term priorities
• Proficiency with Microsoft Office Suite; experience with computerized management systems a plus
• Familiarity with cGMP regulations highly desirable
• Ability to work in both office and laboratory environments