Medical Device CAPA SME

Boston, MA

Job ID: 130479 Industry: Med

 

Medical Device CAPA SME 

Environment:
Our client is a large medical device manufacturer. They manufacture a number of class 1, 2, and 3 medical devices. This person will conduct product and process Corrective and Preventive Action (CAPA) Investigations from Issue identification through Implementation of solution and effectiveness monitoring. 

This individual will be responsible for the following:
• Project manage all aspects of CAPA activity which includes gaining the commitment of cross functional resources, scheduling CAPA team meetings, and providing CAPA deliverables per project timelines. 
Document all phases of CAPA activity in compliance with applicable standards including 21 CFR part 820.1 00 and ISO 13485, and procedural requirements. 
• Maintain CAPA records, keeping them in a state of audit readiness. 
• Lead and mentor cross functional teams with the implementation of appropriate root cause analysis techniques. 
• Analyze quality monitoring data sources and apply statistical techniques to 
identify existing and potential causes of non-conformances. 
• Guide cross functional teams assigned to product CAPA:. to ensure verification and/or validation of corrective and preventive actions are effective and do not adversely affect the finished product. 
• Work effectively with all levels of management to ensure CAPA action plans can be supported and that costs/resources needed to implement the plan are available. 
• Provide periodic CAPA trending data to management for review. 
• Serve a.s TrackWise tool SuperUser/expert. 

Required:

Medical Device

CAPA 

Remediation

Desired:

Data Analysis 

Job Type: Contract 

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