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Quality Control Analyst I

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Los Angeles, CA

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Job Description
Quality Control Analyst ILos Angeles, CA Summary:Conduct specific biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) and medical devices through all stages of the manufacturing process from incoming raw materials to finished goods, and may include environmental monitoring programs. Essential Duties and Responsibilities:\tConduct critical biological, chemical and physical analyses such as raw materials, initial, in-process and final products, and samples collected from environmental monitoring programs at manufacturing facilities, etc.\tUse a variety of laboratory instrumentation and computer systems to collect and record data (such as LIMS system). Perform assays requiring precise analytical skills and understanding of biology and chemistry principles.\tComplete all testing, including special project / protocol testing in a timely and appropriate manner.\tMaintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations.\tWrite exception documents.\tParticipate in functional efforts involving teams, which impact production, increase efficiency, solve problems, generate cost savings and improve quality.\tPerform laboratory and manufacturing audits as required. Audit and update, as required, plant SOPs.\tMay perform equipment maintenance and calibrations as required. May perform other duties as assigned.Qualifications:\tAbility to handle multiple tasks concurrently, and in a timely fashion.\tComputer literate. Must be detail oriented, conscientious and have high reading comprehension skills.\tMust have basic understanding of laboratory instrumentation.\tMust be able to communicate effectively with supervisors and peers.\tMust be able to read, write, and converse in English.\tMust be able to navigate, conduct searches, and fill on line forms on Personal Computer for the purposes of training, performance management, and self-service applications.\tMust have the ability to navigate electronic mail systems and intranet for communication purposes.\tGood interpersonal skills and be able to work effectively and efficiently in a team environment.\t Knowledge of cGMP manufacturing.\tKnowledge of basic laboratory and pharmaceutical production equipment including but not limited to: autoclaves, process tanks, incubators, analytical equipment, and CIP/SIP systems.\tKnowledge of basic chemical and biological safety procedures.\tMust be able to read and follow detailed written instructions and have good verbal/written communication skills.\tMust have the following personal attributes: integrity and trust, work ethic, sound judgment, intellectual honesty, pragmatism, courage and conviction.\tMust have passion to innovate and drive for solutions.\tMust display personal accountability for results and integrity.\tMust display eagerness to learn and continuously improve.\tMust have uncompromising dedication to qualityEducation:\tBachelor’s Degree in Chemistry, or Biological Sciences with Analytical Chemistry or Laboratory coursework with 0-2 years’ experience.\tAppropriate additional certifications may be required pursuant to state or federal regulatory requirements

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Atos SE (Societas Europaea) is a leader in digital services with 2014 pro forma annual revenue of circa € 11 billion and 93,000 employees in 72 countries. Serving a global client base, the Group provides Consulting & Systems Integration services, Managed Services & BPO, Cloud operations, Big Data & Cyber-security solutions, as well as transactional services through Worldline, the European leader in the payments and transactional services industry. With its deep technology expertise and industry knowledge, the Group works with clients across different business sectors: Defense, Financial Services, Health, Manufacturing, Media, Utilities, Public sector, Retail, Telecommunications, and Transportation.

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