Quality Coordinator

Responsibilities Support the cGMP compliant quality program for pharmaceutical storage Work in collaboration with Emergency Preparedness and Response Manager, Operations Manager, Program Manager, and Compliance Manager Maintain and enhance the quality management system (MasterControl) Ensure consistent quality practices across all distribution operations Serve as a functional member of the Quality team to manage MasterControl, including document control, training, change control, and other cGMP workflows Participate in the development, maintenance, and documentation of policies, procedures, and work instructions within the Quality Management Program Schedule, participate in, and review internal quality audits and related meetings Support external audits with customers, regulatory bodies, and third-party auditors and track audit findings with assisting in timely implementation and verification of corrective actions Serve as the internal point of contact for documenting and tracking ongoing performance issues Support root cause analysis efforts to help develop effective corrective and preventive actions (CAPA) Act as liaison with customers and vendors regarding quality issues, investigations, and corrective actions Conduct vendor qualification activities and review annual vendor requalification documentation Assist with future validations or revalidations of systems, equipment, or processes Verify Preventive Maintenance activities are completed in accordance with contractual agreements Collaborate with functional and departmental managers to support new programs and change management of existing processes Maintain and enhance the training reference material and training program by ensuring training assignments are current and completed for new hires and existing employees Perform additional responsibilities as assigned to support the Quality and Compliance program Requirements Bachelor’s Degree in technical discipline (science or engineering) or related field; or equivalent combination of education and experience Minimum of 3 years of experience in quality management at an ISO certified or FDA regulated drug, biologic, or medical device manufacturer or distribution center Experience with Master Control Quality Management software or MasterControl is strongly preferred Proficient in Microsoft Office, including strong Word, Excel, and Outlook Must have excellent communication skills, both written and verbal Ability to communicate with individuals at all levels of an organization Must have strong math and computer skills Must have knowledge using an ISO quality system or cGMP quality system in a storage or distribution facility Ability to multi task and be forward thinking Successfully pass a pre-employment (post offer) background check and drug screening #J-18808-Ljbffr Jobtailor