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Manager Site Quality Assurance
full-timeSt. Paul$99k - $198k

Summary

Location

St. Paul

Salary

$99k - $198k

Type

full-time

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About this role

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 114,000 colleagues serve people in more than 160 countries.

     

JOB DESCRIPTION:

Job Title

Manager, Site Quality Assurance
 

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. You’ll also have access to:

  • Career development with an international company where you can grow the career of which you dream.
  • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
  • An excellent retirement savings plan with high employer contribution
  • Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
  • A company recognized as a great place to 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

This position works out of our St. Paul, MN (New Brighton) location in the Abbott Vascular division. 

As the Site Quality Assurance Manager, you’ll have the chance to ensure that systems, processes, and staffing are suitably designed and implemented to maintain an effective/active quality system. The Site Quality Manager will work with their group to: Ensure product safety, reliability and quality through the effective use of quality planning, risk analysis, statistical methods and process controls during the design and manufacturing stages of the product.

What You’ll Do

  • Reduce costs by employing Quality/Reliability System Processes that result in the development of efficient test and inspection plans, improved yields, and minimized scrap.
  • Communications with regulatory authorities.
  • Recruits, coaches and develops organizational talent.
  • Minimize the number of field events through effective analysis of returned products, corrective actions and timely investigation and response to field events.
  • Ensure efficient compliance to all applicable regulations through the implementation of a robust quality system and through communication/reporting to regulatory authorities.
  • Exceed customer expectations by ensuring excellent investigation to field events in a professional and timely manner.
  • Fosters a diverse workplace that enables all participants to contribute to their full potential in pursuit of organizational objectives.
  • Creates an entrepreneurial environment.
  • Provides direction and guidance to exempt specialists and/or supervisory staff who exercise significant latitude and independence in their assignments.
  • Supervise exempt and non-exempt employees.
  • Keeps the organization's vision and values at the forefront of decision making and action.
  • Demonstrates effective change leadership.
  • Builds strategic partnerships to further departmental and organizational objectives.
  • Develops and executes organizational and operational policies that affect one or more groups by utilizing technical/professional knowledge and skills.
  • Monitors compliance with company policies and procedures (e.g. compliance with FDA, BSI, EEO regulations, etc.).
  • Makes decisions regarding work processes or operational plans and schedules in order to achieve department objectives.
  • Develops, monitors and appropriately adjusts the annual budget for department(s).
  • Provides appropriate level of cross-functional and customer-oriented communications regarding the status of department and quality system operation, as well as product performance.
  • Develops, communicates, and builds consensus for operating goals that are in alignment with the division.
  • Provides leadership to assigned staff and supervisors by communicating and providing guidance towards achieving department objectives.
  • Creates immediate to long-range plans to carry out objectives established by top management; develops and calculates a budget for a department or group to meet organizational goals; forecasts future departmental needs including human and material resources and capital expenditures; recommends or modifies the structure of organizational units or a centralized functional activity subject to senior management approval.
  • Assignments are expressed in the form of objectives; makes decisions regarding work processes or operational plans and schedules in order to achieve the program objectives established by senior management; consequences of erroneous decisions or recommendations would normally include critical delays and modifications to projects or operations with substantial expenditure of time, human resources, and funds, and may jeopardize future business activity.

Required Qualifications

  • Bachelors Degree in Chemistry, Biology, Engineering or other technical discipline.
  • Minimum 7 years’ related work experience.

Preferred Qualifications

  • Medical device industry experience, highly preferred.

Apply Now

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:  www.abbottbenefits.com

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.

     

The base pay for this position is

$99,300.00 – $198,700.00

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

     

JOB FAMILY:

Operations Quality

     

DIVISION:

AVD Vascular

        

LOCATION:

United States > Minnesota > St. Paul : 1225 Old Highway 8 NW

     

ADDITIONAL LOCATIONS:

     

WORK SHIFT:

Standard

     

TRAVEL:

Yes, 10 % of the Time

     

MEDICAL SURVEILLANCE:

No

     

SIGNIFICANT WORK ACTIVITIES:

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)

     

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

     

EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEOEnglish.pdf

     

EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEOSpanish.pdf

Other facts

Tech stack
Quality Assurance,Risk Analysis,Statistical Methods,Process Controls,Regulatory Compliance,Coaching,Talent Development,Field Event Analysis,Budget Management,Cross-Functional Communication,Change Leadership,Strategic Partnerships,Operational Policies,Product Safety,Reliability,Quality Planning

About Abbott

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, nutritional and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.

Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and www.facebook.com/AbbottCareers, on Instagram @AbbottGlobal, and on X @AbbottNews.

We invite you to explore opportunities at Abbott, to see if your talents and career aspirations may fit with our openings. An equal opportunity employer, Abbott welcomes and encourages diversity in our workforce.

Terms of Use: https://www.abbott.com/social-media-terms-of-use.htm

Team size: 10,001+ employees
LinkedIn: Visit
Industry: Hospitals and Health Care

What you'll do

  • The Site Quality Assurance Manager ensures that systems, processes, and staffing are effectively designed and implemented to maintain a robust quality system. Responsibilities include ensuring product safety and compliance with regulations, as well as leading and developing the quality assurance team.

Ready to join Abbott?

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Frequently Asked Questions

What does Abbott pay for a Manager Site Quality Assurance?

Abbott offers a competitive compensation package for the Manager Site Quality Assurance role. The salary range is USD 99k - 199k per year. Apply through Clera to learn more about the full compensation details.

What does a Manager Site Quality Assurance do at Abbott?

As a Manager Site Quality Assurance at Abbott, you will: the Site Quality Assurance Manager ensures that systems, processes, and staffing are effectively designed and implemented to maintain a robust quality system. Responsibilities include ensuring product safety and compliance with regulations, as well as leading and developing the quality assurance team..

Why join Abbott as a Manager Site Quality Assurance?

Abbott is a leading Hospitals and Health Care company. The Manager Site Quality Assurance role offers competitive compensation.

Is the Manager Site Quality Assurance position at Abbott remote?

The Manager Site Quality Assurance position at Abbott is based in St. Paul, Minnesota, United States. Contact the company through Clera for specific work arrangement details.

How do I apply for the Manager Site Quality Assurance position at Abbott?

You can apply for the Manager Site Quality Assurance position at Abbott directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about Abbott on their website.