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Agilent Technologies Quality Control Analyst (2nd Shift) in Frederick, Colorado

Job FunctionQuality/RegulatoryTravel RequiredNoJob DescriptionAgilent inspires and supports discoveries that advance the quality of life. Weprovide life science, diagnostic and applied market laboratories worldwidewith instruments, services, consumables, applications and expertise.Agilent enables customers to gain the answers and insights they seek so theycan do what they do best: improve the world around us. Information aboutAgilent is available at www.agilent.com.Agilent Technologies, Inc. is looking to add a Quality Control Analyst toits high-performance quality team working at the state-of-the-art, contractAPI manufacturing facility that specializes in Nucleic Acid Chemistrieslocated in Frederick, Colorado.The world's most revolutionary biopharma companies are partnering withAgilent Technologies to advance the next frontier of medicine. Agilentcontinues to invest in the capacity and expansion of its Colorado operations.Join our team of professionals dedicated to the development andcommercialization of nucleic acid therapeutics for life-changing,life-saving medicines.This position coordinates and conducts routine and non-routine testingsupport. Responsibilities include testing to support manufacturing, rawmaterial release, qualification, and validation activities. Understandingand experience with Standard Operating Procedures, current GoodManufacturing Practices (cGMPs) and other regulatory requirements arerequired.This will be a second shift position; hours will be 2 pm-11 pm Monday-Friday.ESSENTIAL DUTIES AND RESPONSIBILITIES:Exercises judgment within broadly defined practices and policies in selectingmethods, techniques and evaluation criteria for obtaining resultsOutstanding communication skills, both written and oral, and the abilityto communicate directly with peers and area managersConducts analysis associated with clinical and non-clinical laboratory studiesunder current Good Manufacturing Practices (cGMP) regulations and guidanceper Food and Drug Administration (FDA) and Organization for EconomicCo-Operations and Development (OECD) as well as International regulationsPerforms analysis on raw materials, in-process materials, APIs(developmental and commercial), final product and other requestedtesting as per written procedures.Reviews data for compliance to specifications, report results, andtroubleshoots abnormalitiesEnsures equipment is performing well and communicates and takes appropriateaction as necessaryTroubleshoots, investigates, and resolves laboratory testing failures anddrives solutions to improve the quality control laboratory programs throughcorrective and preventive actionsMaintains inventory and ordering of laboratory suppliesPerforms maintenance activities on laboratory instruments and equipmentEnsures good documentation practices are followedWorks cross-functionally to complete projects and testing.Job TypeExperiencedShiftSwing ShiftQualifications2+ years of relevant experience for entry to this levelBachelor's degree (B.S.) or equivalent experience in Chemistry orrelated life sciences field with one to three years related experienceand/or training; or equivalent combination of education and experience.Proven knowledge of cGMP guidelines as well as international regulations(i.e., International Committee on Harmonization (ICH) Q7) pertainingto Quality Control programs that support the production of APIs, stabilityand drug product release.Demonstrated knowledge of analytical equipment and... For full info followapplication link.Agilent Technologies, Inc. is an Equal Employment Opportunity andAffirmative Action employer. We value diversity at all levels. Allindividuals, regardless of personal characteristics, are encouraged to

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