Manager, Quality Manager CAPA

Abbott


Job Location:

Columbus, OH - USA

Monthly Salary: $ 129300 - 258700
Posted on: Yesterday
Vacancies: 1 Vacancy

Job Summary

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare with leading businesses and products in diagnostics medical devices nutritionals and branded generic medicines. Our 115000 colleagues serve people in more than 160 countries.

JOB DESCRIPTION:

Quality Manager CAPA

Working at Abbott

At Abbott you can do work that matters grow and learn care for yourself and family be your true self and live a full life.Youllalso have access to:

  • Career development with an international company where you can grow the career you dream of.

  • Free medical coverage for employees* via the Health Investment Plan (HIP) PPO

  • An excellent retirement savings plan with high employer contribution

  • A company recognized asa great placeto work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.

  • A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity working mothers female executives and scientists.

The Opportunity

The function of the Quality Manager CAPA is to provide corporate-level leadership and guidance for Quality Systems matters related tononconformance investigation andCorrective AndPreventiveAction (CAPA) processes and other related Abbott Quality System elements. This includes Business/Division support quality and technicalexpertiseandconsulting activities globally. The incumbent must have a working knowledge of global regulations and industry standards related to nonconformance investigation and Corrective And Preventive Action (CAPA) processes. The incumbent should also haveworkingknowledge and understand the relationship to other related Quality System elements e.g. management responsibility risk management complaint management design controls validation etc.

This rolewillbe based out ofAbbott Park Il

What Youll Work On

  • Use established management skills to lead global committees and teams to achieve qualitysystems objectivesinclusive of training evaluation of effectiveness of business application of the nonconformance/CAPAprocesses andimplementation of necessary requirements into the corporate wide quality management systemregulatory compliance and businessobjectives.

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

  • Remain current on regulatory requirements best practices and regulatory agency expectations to drive updates in corporate policies and procedures asappropriate.

  • Participate in industry groups related to the subjectmatterareas of responsibility.

  • Improve the effectiveness of Abbotts Quality Systems through monitoringtrendingandanalyzingquality data and industry intelligence information.

  • Act as a change agent for incorporating best practice methods through business support activities such as remediation training coachingcontinuous improvement initiativesetc.

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

  • This position manages multiple global projects particularlyinnonconformance investigationcorrective andpreventive action including leadership of the Nonconformance and CAPA community of practice (CoP).

  • Active leadership and participationand analysis of nonconformance and CAPA quality dataand assessments.

  • 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

  • This position manages confidential information across the project lifecycle.

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

Required Qualifications

  • Bachelors Degree; Life or Engineering Sciences discipline preferred.

  • Overall10 years of experience with 6 years innonconformance and CAPAprocesses root cause analysis toolsquality systemcontinuous improvementexperience in a regulated industry.

  • 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 ispreferred butnot).

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

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The base pay for this position is

$129300.00 $258700.00

In specific locations the pay range may vary from the range posted.

JOB FAMILY:

Operations Quality

DIVISION:

AQR Abbott Quality and Regulatory

LOCATION:

United States > Abbott Park : AP52

ADDITIONAL LOCATIONS:

WORK SHIFT:

Standard

TRAVEL:

Yes 50 % of the Time

MEDICAL SURVEILLANCE:

No

SIGNIFICANT WORK ACTIVITIES:

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day) Keyboard use (greater or equal to 50% of the workday)

Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.

EEO is the Law link - English: EEO is the Law link - Espanol: Experience:

Manager

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare with leading businesses and products in diagnostics medical devices nutritionals and branded generic medicines. Our 115000 collea...

About Company

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WHO WE ARE CREATING LIFE-CHANGING TECHNOLOGY From removing the regular pain of fingersticks as people manage their diabetes to connecting patients to doctors with real-time information monitoring their hearts, from easing chronic pain and movement disorders to testing half the world’s ... View more

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