Sr Manager, Quality Data Analytics

PURPOSE AND SCOPE:

Develops, implements, and maintains the activities of quality systems.

Oversees development and implementation of standards, methods, and procedures for inspecting, testing, and evaluating the precision, accuracy, and reliability of company products.

Makes recommendations for corrective action necessary to ensure conformity with quality specifications.

Ensures finished products conform to government and company standards and satisfy good manufacturing practices regulations.

 

PRINCIPAL DUTIES AND RESPONSIBILITIES:

​​Data Analytics:


* ​Leads efforts to develop system resolutions to report the credible data. 


* Analyze quality data reports for various internal customers and forums. 


* Generates advanced analytics and research from both external and internal data sources. 


* Assess potential product risks (from data reporting, prediction of performance and/or market observation and identified quality problems) 


* Provide support during creation and maintenance of quality reporting for leadership 


* Investigates complex data related issues and synthesizes quantitative and qualitative information using past, current, and future trending information. 


* One off report generation supporting business decisions or specific leadership requests. 


* Initiate analyses and investigations in terms of quality events/reports.


* Create actionable trend information and ensure that internal members of the company have the information necessary to make informed business, operating, and research decisions. 


* Ensure the appropriate timeliness, usability, and accuracy of the reports. 


* Measure and report the global quality performance of products and processes, through the product lifecycle, through the deployment of a global predictive reporting mechanism. 


* Audit quality data inputs for accuracy and consistent application of required measures. 


* Utilization of predictive analytics will support the identification and reporting of potential and actual quality related events. 


* Ensure the quality measurement system is consistently applied across global sites and validated/verified per regulatory requirements. 


* Deploy and maintain the global quality performance tracking and reporting process and tools supporting vertical (InCenter) global medical devices product conformity. 


* Establish best in class predictive quality product performance indicators and analytics globally across sites and products. 


* Interface with design and operations quality, and other functions, globally to ensure product performance and regulatory impacting measures are consistently gathered, reported, and analyzed. 

 

CAPA:


* Support evaluation and categorization of NC/CAPAs based on severity/criticality of the related


* Event.

(Re-) Allocation of NC/CAPAs to involved parties and Investigation Units


* Follow up of NC/CAPA records regarding ti...