Quality Control Analyst

Quality Control Associate IIA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionPosition Details:Client Direct ClientLocation Research Triangle Park, NCJob Title Quality Control Associate IIDuration 1 Year+Must have skill-set [Job Description] Primary ResponsibilitiesThe primary responsibilities for a Quality Control Associate II include:The execution of QC routine testing to include TOC, conductivity, and nitrates.In addition, the Associate II will be responsible for executing TOC method validations and all associated activities.All activities are executed in a cGMP manner.Additional responsibilities include, but are not limited to, data review/analysis, analytical/technical support and problem solving capabilities, technical writing skills, support of method transfer, execution of robust and compliant cGMP documentation practices, and an understanding of FDA/EMEA regulations.An Associate II will adhere to the Quality Systems and apply them, as appropriate, to daily functions.The Associate II will proactively communicate with direct management regarding cGMP compliance and identification of issues and/or corrective actions on the laboratory floor.The Associate II will be able to work effectively within the group to promote robust teamwork by having both verbal and written communication skills.The Quality Control Associate II will possess demonstrated technical ability regarding fundamental laboratory techniques, analytical methodology, and method validation.The position requires but is not limited to the following: Understanding of basic biological science principles; ability to communicate with peers and management; effective organizational skills; ability to multi-task and coordinate multiple activities in parallel; developing or demonstrated instrument/method troubleshooting and problem solving skills; general knowledge of FDA/EMEA regulations and compliance.QualificationsEducation• B.S. degree (biological science preferred; 3-5 years of relevant experience)