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QC Associate I (272207)

ASK Consulting
Vacaville, CA Contractor
POSTED ON 12/16/2025
AVAILABLE BEFORE 2/15/2026
"All candidates must be directly contracted by ASK Consulting on their payroll and cannot be subcontracted. We are unable to provide sponsorship at this moment".Job Title: QC Associate ILocation: Vacaville, CA, 95688 (onsite)Duration: 6 MonthsPR: $25  - $27.93/hr on W2 AIJob description:With limited supervision, QC Associate I, is responsible for the performance of direct materials testing in accordance with cGMP regulations. These duties include execution of laboratory testing, trend analysis, documentation review, support of discrepancies (OOS, OOT, OOE) and other laboratory support activities. In conjunction with Quality Control leadership, the QC Associate II works to meet departmental and organizational goals.Job Requirements:B.S./B.A. degree and 1-3 years experience or Masters Degree plus one year experience or an equivalent combination of education and experience.Degrees are preferably in relevant scientific disciplines and experience is in the pharmaceutical or biopharmaceutical industry.Strong verbal and written communication skills, ability to organize and present information both formally and informally.Demonstrated ability to apply knowledge of scientific theories, principles, and techniques used in analytical or biological test procedures.Routinely exercises sound judgment, reasoning and problem solving.Capable of working under limited supervision and determining own short term priorities.Job Responsibilities:Perform a broad variety of basic and moderately complex tests with documentation according to GMPReview data and assess against established acceptance criteriaPerform technical review of peer-generated dataEvaluate data to identify trends and/or establish limitsIdentify discrepancies; provide input to design of quality investigations and CAPA (corrective actions preventive actions) initiatives as neededIdentify and troubleshoot technical problemsIdentify gaps in systems and proceduresReceive and provide trainingParticipate in assay transfer and assay validationPerform equipment qualification / maintenancePrepare and maintain standards, controls, stocks, cultures, etc. per established proceduresSupport the maintenance and compliance of operational areasAssure and apply GMP throughout operationsCoordinate with customers to support multi-site operational activitiesSupport internal and external audits and regulatory inspectionsWorks to meet schedules, timelines, deadlinesParticipate in and/or lead group and project teamwork; project and process improvementsWrite protocols and reports under limited supervisionMeets scheduled performance of 95% on timePerform other duties as requested by managers to support Quality activitiesAbout ASK: ASK Consulting is an award-winning technology and professional services recruiting firm servicing Fortune 500 organizations nationally. With 5 nationwide offices, two global delivery centers, and employees in 42 states-ASK Consulting connects people with amazing opportunitiesASK Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all associates.

Salary : $25 - $28

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