2nd Shift Quality Control Technician

2nd Shift Quality Control TechnicianLiquid and Topicals Division MD - Easton, MD 21601OverviewSalary Range $18.00 - $20.00 Hourly Position Type Full Time Job Shift Any Category ManufacturingQuality Control Technician 2nd ShiftCome join our growing team!!!QualificationsCore Quality FunctionsAssist with the inspection of incoming components according to documented specifications.Assist with the generation and approve controlled labels using programs provided.Record data and maintain accurate records in accordance with cGMP current good documentation practices for accuracy and completeness.Retrieval of documents using the EQMS computer system.Troubleshoot quality concerns that may arise during incoming components and report to Quality Manager.Verify the calibration of all inspection test equipment and maintain accurate records.Perform data entry and retrieval using the Aphena computer systemMay be required, as needed, to work overtime, weekends or alternate shifts.Assist in the generation and resolution of corrective and preventive action plans (CAPAs)Assist in the documentation and resolution of nonconforming material reports and process discrepancy reports.Ensure nonconformances are initiated and reported promptly.If necessary, initiate non-conforming or process discrepancy documentationMaintain work area orderliness and cleanliness.Assist in maintaining compliance within the quality system.Ensure that the test equipment is maintained and records kept.Ensure equipment is calibrated before use.Written and verbal communication skills are required to communicate issues and procedures among multiple departments.Ability to interact with other co-workers at a professional levelJob requires data entry [writing] that requires neatness and accurate records.Knowledge of Current Good Manufacturing Practice {cGMP) Regulations pertaining to medical devices and pharmaceuticals.Manage daily activities to ensure support for business operations.Ensure paperwork is completed within a timely manner and complies with cGMP.Determine root cause and corrective and preventive action plan for any Investigations, CAPA, and 005 issues related to the area of responsibility and complete related documentation.Maintain operational efficiency and compliance with all test equipment and processes.Provide the necessary QA support needed for the rapid commercialization of new products and processes.Perform/assist in any required cGMP validations.Review in process batch records and equipment notebooks daily.Ability to work With Microsoft Excel, Word, and PowerPoint.Serve as backup for QA Technician when needed.