QA Specialist

Audit bioanalytical data and reports. Conduct in-process inspection, conduct on-site facility inspections, consult with facility personnel and serve as a resource on the interpretation and application of regulations.Comply with Quality Assurance related Ba Research Standard Operation Procedures.Participate and assist with regulatory inspections and sponsor visits as needed.Prepare and retain written reports on audits, inspections and disseminate them to management, study directors and appropriate personnel.Provide management with reports on quality assurance activities.Review facility standard operation procedures for compliance and provide in-put in updating the standard operation procedures.Assure that the calibration schedule for equipment is followed. Maintain the calibration records in QA.Supply Quality Assurance statements for final reports, support computer validation and equipment validation activities, as well as other duties as assigned. REQUIREMENTS
A minimum of B.S. in Biology or related science Knowledge of GLP/GMP regulations and direct exposure to the procedures used in the conduct of non-clinical studies Must be familiar with Microsoft Word and Excel Organized and be able to multi-task efficiently