what in All Locations Alaska Alabama Arkansas Arizona California Colorado Connecticut District of Columbia Delaware Florida Georgia Hawaii Iowa Idaho Illinois Indiana Kansas Kentucky Louisiana Massachusetts Maryland Maine Michigan Minnesota Missouri Mississippi Montana North Carolina North Dakota Nebraska New Hampshire New Jersey New Mexico Nevada New York Ohio Oklahoma Oregon Pennsylvania Puerto Rico Rhode Island South Carolina South Dakota Tennessee Texas Utah Virginia Vermont Washington Wisconsin West Virginia Wyoming       Quality Assurance Engineer II Supporting 3rd Shift Job Company - Watson Pharmaceuticals Location -  Corona, California  US   Job Code - 7782BR Position - See Job Description Job First Active on: Friday, August 26, 2011 Quality Assurance Engineer II (Supporting 3rd Shift) Watson Pharmaceuticals, Inc. (NYSE: WPI) is a leading integrated global pharmaceutical company engaged in the development, manufacturing, marketing, sale and distribution of generic, brand and biologic pharmaceutical products. We operate and manage our business as three operating segments: Global Generics, Global Brands and Anda Distribution. Our largest commercial market is the United States, followed by our key international markets including Western Europe, Canada, Asia/Pacific, South America and South Africa. As of December 31, 2010 we marketed approximately 160 generic prescription pharmaceutical product families and approximately 30 brand pharmaceutical product families in the U.S., and a significant number of product families internationally. Our Anda Distribution Division distributes products for over 200 suppliers and is focused on providing next-day delivery and responsive service to its customers In terms of our culture, we focus on Our Winning Behaviors – simple, universal words that speak volumes about how we act and what we do. Challenge – Connect – Commit. Our Winning Behaviors require effort from each of us – effort to live them, embrace them, and personalize them. Our Winning Behaviors define the actions we take individually, and as a team, in pursuing our global mission and vision. Our Winning Behaviors are who we are, what we do and how we act. Do you embrace Our Winning Behaviors? If yes, keep reading to consider if you would like to apply to become a part of our team! Under general supervision, coordinates investigations into product complaints.Authors and compiles Annual Product Reviews and generates quarterly and yearly Quality Review Reports. Monitors and trends key areas and indicators from production and laboratories for implementation of corrective and preventative measures. Analyzes data from production and laboratories, and reports anomalies.Monitors activities in key areas for compliance to standards and opportunities for Coordinate investigations and writes final reports for product complaints. Authors Annual Researches and recommends improvements in production and laboratory systems.May review, approve and support execution of validation protocols and master plans.Complies with all Company policies and procedures, including safety rules and Performs related duties as assigned. Carries out responsibilities in accordance with the organization's policies, procedures, and state, federal and local laws. Complies with all Company policies and procedures, including safety rules and regulations. Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements in a regulated manufacturing environment. REQUIREMENTS - QUALIFICATIONS: Quality Assurance Engineer II (Supporting 3rd Shift) Must Have Knowledge Of : Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements in a regulated manufacturing environment. OSHA, FDA, EPA, AQMD and other applicable regulatory and safety compliance guidelines.Applied cGMP's and Company systems.Laboratory equipment and testing. Auditing techniques in a regulated environment.Applied statistics and trend analysis.Pharmaceutical manufacturing, its customers, competition and market.Preparation and presentation of Annual Product Reviews (APR’s). Compilation of data investigation of Product Complaints.Pharmaceutical manufacturing suppliers, raw materials and products.New and emerging inspection and test technology.English usage, spelling, grammar and punctuation.Engineering and business computer systems and software applications. Investigations to determine cause, corrective action and prevention planning Bachelor's Degree in Science, Engineering or related field from an accredited college or university, and a minimum of two (2) – four (4) years related experience preferably in a quality assurance environment; or, an equivalent combination of education and/or experience. Watson Pharmaceuticals Apply to this job! View Company Jobs Free Career Test Your Resume on 75 Job Sites

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