Manager, Quality Manager - CAPA

Required Qualifications

• Bachelor’s Degree required; Life or Engineering Sciences discipline, preferred. 

• Overall 10+ years of experience with 6 years in nonconformance and CAPA processes, root cause analysis tools, quality system continuous improvement experience in a regulated industry required.  

• 4 years in Quality Assurance and/or Compliance, managerial, supervisory or SME role; 10+ years in Medical Device, Pharmaceutical and/or Nutritional industry professional-level position.  

• 3 years of project management experience (certification is preferred but not required). 

• 10-12 years (not necessarily the sum of the above) Total combined minimum years of industry experience required.  

What You'll Work On

1. 1

   Use established management skills to lead global committees and teams to achieve quality systems objectives, inclusive of training, evaluation of effectiveness of business application of the nonconformance/CAPA processes and implementation of necessary requirements into the corporate wide quality management system, regulatory compliance, and business objectives. 

1. 2

   Act as the corporate liaison to Abbott Businesses/Divisions and provide support as an expert in the subject matter of nonconformance, investigation and CA/PA elements. 

1. 3

   Remain current on regulatory requirements, best practices, and regulatory agency expectations to drive updates in corporate policies and procedures as appropriate.  

1. 4

   Participate in industry groups related to the subject matter areas of responsibility.  

1. 5

   Improve the effectiveness of Abbott’s Quality Systems through monitoring, trending and analyzing quality data and industry intelligence information.  

1. 6

   Act as a change agent for incorporating best practice methods through business support activities such as remediation, training, coaching, continuous improvement initiatives, etc.  

1. 7

   The scope of this position is Abbott-wide, covering all Abbott Businesses / Divisions.  

1. 8

   This position manages multiple global projects, particularly in nonconformance, investigation, corrective and preventive action including leadership of the Nonconformance and CAPA community of practice (CoP).  

1. 9

   Active leadership and participation and analysis of nonconformance and CAPA quality data and assessments.  

1. 10

   Given the nature of the projects as they relate to regulatory and quality compliance, the financial consequences for adverse regulatory findings or delayed product approval initiatives can be significant 

1. 11

   This position manages confidential information across the project lifecycle. 

1. 12

   This position requires significant interaction with executive management with accountability for assigned projects.