Job Details

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.#J-18808-Ljbffr