Sr. Quality Records Investigator

Technical writing for the educated but uninformed reader, translate difficult and complex scientific events into a brief and cohesive report as a finished product. Accurately capture immediate actions and containment of the event, address comments from both internal and external clients on the compiled final report. Gathering Data from various sources across the site, performance of Root Cause Analysis (RCA) to determine the most likely cause of the deviation investigation, assessment of event for impact to Safety Identity Strength Quality Purity (SISQP), perform trending analysis, identification of Corrective and Preventative Actions to reduce deviation recurrence, performance of Risk Assessments, Causing Mapping, Interviewing.

Management of multiple projects and timelines concurrently. Ability to adhere to standard timeline, and esc… actions appropriately for resolution in a timely manner. Participation in the Daily Management meetings to update leadership or current deviation statuses.

Routine interaction with the customer, including compilation of Power Points to communicate investigational current status, Alignment meetings, facilitated reviews, CAPA discussions, Comments resolution.

Work on the manufacturing floor for data gathering, observing of processes for investigations, and performance of associate interviews. Meeting Facilitation and participation, aligning internal review team and area subject matter experts on an agreed to investigational path forward. Complex Conflict resolution, problem solving in a cross functional setting, and ability to keep the meeting on track to achieve objectives of varying difficulty.

Attendance and occasional leadership of the daily management system and participating/leading the deviation review board.

Perform other duties as assigned.

Investigations CAPA Root Cause Analysis (RCA)