Quality Control Technician

Job Title QC Analyst I Duration 6 Months (possibility of extension) Summary With limited supervision, the QC Associate I is responsible for performing direct materials testing in accordance with cGMP regulations. These duties include executing laboratory testing, conducting trend analysis, reviewing documentation, supporting 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 Responsibilities Perform a broad variety of basic and moderately complex tests with documentation according to GMP Review data and assess against established acceptance criteria Perform technical review of peer-generated data Evaluate data to identify trends and/or establish limits Identify discrepancies; provide input to design of quality investigations and CAPA (corrective actions preventive actions) initiatives as needed Identify and troubleshoot technical problems Identify gaps in systems and procedures Receive and provide training Participate in assay transfer and assay validation Prepare and maintain standards, controls, stocks, cultures, etc. per established procedures Support the maintenance and compliance of operational areas Assure and apply GMP throughout operations Coordinate with customers to support multi-site operational activities Support internal and external audits and regulatory inspections Works to meet schedules, timelines, deadlines Participate in and/or lead group and project teamwork; project and process improvements Write protocols and reports under limited supervision Meets scheduled performance of 95% on time Perform other duties as requested by managers to support Quality activities Job Requirements B.S./B.A. degree and 1-3 years experience or Master's 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. Hourly Rate $26-$27.93 per hour. Compensation Factors which may affect starting pay within this range may include [geography/market, skills, education, experience, and other qualifications of the successful candidate]. Benefits Sunrise offers ACA compliant medical coverage/dental insurance/vision insurance to all employees. We also offer Sick time benefits as required per State regulations. Seniority Level Entry level Employment Type Contract Job Function Research and Science Industries Pharmaceutical Manufacturing, Biotechnology Research, and Medical Practices #J-18808-Ljbffr Sunrise Systems, Inc.