What are the responsibilities and job description for the QA Specialist position at Fagron GmbH & CO. KG?
The Quality Assurance Specialist is an intermediate level professional position responsible for quality assurance activities associated with cGMP manufacturing, documentation, and product disposition. Ensures that proper controls are followed and maintained during the manufacturing, processing, packaging, and warehousing of compounded products.Key ResponsibilitiesExecute and develop proficiency in all Level 1, Level 2, and Level 3 Quality Assurance tasks : Level 1 : Manufacturing / Packaging Line ClearancesProduct Label Review and ApprovalProduct Label ReconciliationEMS Data ReviewLogbook Review and reconciliationLevel 2 : Batch Record IssuanceBatch Record Review and ApprovalIncoming Material Review and ApprovalForm and Logbook IssuanceReview and Approval of Testing DataReview and Approval of Event Reports and Associated Corrective ActionsLevel 3 : Disposition and Release of Incoming MaterialsDisposition and Release of Finished ProductDocument Control ActivitiesReview and Approval of Change Controls and controlled document changesSpecial Projects as assignedReview and Approval of Moderate Risk DeviationsSupport execution of product Batch Records and associated manufacturing and Quality related systems for the compounding processes.Ensure day-to-day compliance to all requirements established for compounded product and the systems supporting compounding.Assist with problem identification and resolution efforts for quality related issues associated with the compounding operations.Assist with internal, corporate, 3rd party and federal / state inspections and audits.Provide contributing information on measures of local quality system effectiveness such as right the first time, documentation errors and others as assigned.Ensure cGMP documentation associated with work activities meets ALCOA standards.Maintain assigned training standard operating procedures.Perform other related duties as assigned.Ihr Profil College Degree and at least five to eight years cGMP experience in a pharmaceutical manufacturing company or equivalent combination of education and cGMP experience in a required.Experience with quality systems, aseptic technique, cGMP document review, quality investigations, CAPA, Change Control and MasterControl preferred.Proficient in MS Office programs, including Word and Excel.Ability to process information rapidly from multiple sources and communication channels.Ability to handle a high volume of work and rapidly adapt to changing environment.We offer a dynamic environment where talent and ambition can develop to its fullest. We have an open and informal organization culture, where individuals need to have strong motivation and ability to work independently.#J-18808-Ljbffr
