Philips Senior QMS & Document Control Specialist in Wallingford, Connecticut
Maintains the document management system and ensure compliance to the applicable standards and regulations.
Overseeing all associated document control activities to ensure program fitness and to help ensure that business goals and objectives are met
Maintain vigilance on key performance indicators (KPIs) for bi-annual documentation review and training completeness
Provide periodic updates and escalations on Document Control matters (e.g. backlogs, project statuses, etc.)
Routinely meet with functional managers to strategize and plan tactics to meet project/business objectives
Collaborate with individuals on select items to resolve issues and to maintain continuity of effort
Maintain weekly Change Control Board meetings to facilitate quicker reviews and continuity of work
Attend project meetings in support of BU/BG goals and Objectives (e.g. MP1, SAP, eDMR)
Responsible for the maintenance and integrity of the Device Master Record, and Quality System documentation.
Responsible for the integrity of the Quality System, Procedures and Forms.
QMS Knowledge is a must.