QA Associate I - Ops (Wed - Sat 6:30 am - 5:00 pm) - (Manchester, NH)

POSITION SUMMARY - This position provides QA support in the manufacturing of clinical and commercial drug products/medical devices to ensure compliance with the principles and guidelines of cGMP. QA Associates maintain the quality systems, such as laboratory control, investigation management, materials management, document control and training to ensure control of the manufacturing process. This position will actively partner with Manufacturing Operations, Facilities, Materials Management, and other supporting departments to provide compliance and technical guidance to ensure quality issues are identified and resolved in a timely manner. POSITION DUTIES - Provide support to all cGMP manufacturing operations in real time on the floor and oversee production activities and monitors dP/NVP as applicable: Responsible for performing routine manufacturing area line clearances Participate in Investigations into Facility, EM, and Utility excursions as assigned