Quality Specialist
Cypress HCM · Irvine, CA
CONTRACT
Posted Sep 8, 2026
Job Description
Core Responsibilities
- Maintain accurate records and follow established quality procedures to support regulatory compliance and audit readiness.
- Review documentation for completeness and compliance with Good Documentation Practices (GDP). Escalate discrepancies to senior team members and organize completed records for filing.
- Assist during audits by retrieving requested documents and conducting preliminary reviews for completeness and GDP compliance.
- Perform routine quality-related tasks under appropriate supervision while developing knowledge of standard quality systems and procedures.
- Maintain a clean, organized, and compliant laboratory environment, including the proper management of materials, supplies, and workspaces.
- Support the Non-Conforming Events Program (NCEP), including CAPAs, deviations, and other quality events.
- Assist with coordinating and executing proficiency testing for required assays.
- Support validation activities, departmental projects, and continuous improvement initiatives as assigned.
- Travel requirement: Less than 10%.
Education And Experience
- Associate degree in a life or physical science field required; bachelor’s degree strongly preferred.
- One to two years of experience working in a molecular laboratory.
Pay Range: 23 - 41/hr
- Maintain accurate records and follow established quality procedures to support regulatory compliance and audit readiness.
- Review documentation for completeness and compliance with Good Documentation Practices (GDP). Escalate discrepancies to senior team members and organize completed records for filing.
- Assist during audits by retrieving requested documents and conducting preliminary reviews for completeness and GDP compliance.
- Perform routine quality-related tasks under appropriate supervision while developing knowledge of standard quality systems and procedures.
- Maintain a clean, organized, and compliant laboratory environment, including the proper management of materials, supplies, and workspaces.
- Support the Non-Conforming Events Program (NCEP), including CAPAs, deviations, and other quality events.
- Assist with coordinating and executing proficiency testing for required assays.
- Support validation activities, departmental projects, and continuous improvement initiatives as assigned.
- Travel requirement: Less than 10%.
Education And Experience
- Associate degree in a life or physical science field required; bachelor’s degree strongly preferred.
- One to two years of experience working in a molecular laboratory.
Pay Range: 23 - 41/hr
Additional Details
- City
- Irvine
- State
- California
- Country
- US
Apply and matching require a free OVN account. Browse listings anytime without signing in.