QC Analyst I

job summary: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.location: Vacaville, Californiajob type: Contractsalary: $23.73 - 27.92 per hourwork hours: 9 to 5education: Bachelorsresponsibilities: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 activitiesqualifications: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.skills: Good Manufacturing Practices (GMP), Corrective and Preventive Actions (CAPA) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. Qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.

Salary : $24 - $28