Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap – Right Talent – Right Time – Right Place – Right Price and acting as a Career Coach to our consultants.
Company: One of Our Clients
Job Description:
Job Title: QC Associate I
Location: Vacaville, CA 95688
Duration: 07+ Months (Extendable)
Pay Rate: $25.00 - 27.93/hr on W2
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.
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
● Perform equipment qualification / maintenance
● 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.
Awards and Accolades:
America's Most Honored Businesses (Top 10%)
Awarded by USPAAC for the Fastest Growing Business in the US
12th Fastest Growing Staffing Company in USA by Staffing industry Analysts in the US (2020, 2019, 2020)
Fastest 50 by NJ Biz (2020, 2019, 2020)
INC 5000 Fastest growing for 8 consecutive years in a row (only 1.26% companies make it to this list)
Top 100 by Dallas Business Journal (2020 and 2019)
Proven Supplier of the Year by Workforce Logiq (2020 and 2019)
2019 Spirit of Alliance Award by Agile1
2018 Best of the Best Platinum Award by Agile1
2018 TechServe Alliance Excellence Awards Winner
2017 Best of the Best Gold Award by Agile1(Act1 Group)
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