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Senior Manager Supplier Quality

Job in Austin, Travis County, Texas, 78716, USA
Listing for: Abbott Laboratories
Full Time position
Listed on 2026-01-07
Job specializations:
  • Quality Assurance - QA/QC
    QA Specialist / Manager, Quality Engineering, Quality Control / Manager
Job Description & How to Apply Below

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.

Sr. Manager, Supplier Quality Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and your 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 you dream of.
  • 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 a high employer contribution
  • Tuition reimbursement, 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 worldwide 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 the best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity

This role manages the Quality System for third party manufacturing in accordance with Corporate and Divisional standards to ensure overall TPM performance and compliance. The role is responsible for keeping all the QS elements consistent and effective for its purpose. Ensures implementation of TPM related Quality Assurance policies and procedures generated conform to predetermined Corporate/Division standards and specifications.

What You'll Work On
  • Manage the Quality System for US third party manufacturing in accordance with Corporate and Divisional standards to ensure overall TPM performance and compliance, systems include:
    • Nonconformance and CAPA
    • Change control
    • Complaints
    • Batch release
    • Label development and control
    • Related budget elements
    • Management reviews
    • Audits
  • Provide quality support for questions related to products compliance queries, complaint investigation, nonconformance and compliance audit preparation.
  • Ensure implementation of TPM related Quality Assurance policies and procedures generated conform to predetermined Corporate/Division standards and specifications.
  • Ensure quality system infrastructure and standards are in place and maintained at US TPMs to meet compliance and timeliness requirements. This is done through the quality systems monthly reviews and MOS tier process, ongoing business maintenance, and tracking and trending.
  • Effectively identifies and develops staffing requirements:
    Develop practices that ensure a diverse workforce and improved job performance.
  • Manage a staff to support batch release, inventory turns, product holds and multi system product traces.
Required Qualifications
  • Bachelor’s degree and minimum 7 Years of experience, both overall and any industry specific experience needed.
  • Strong business acumen and cross functional experience (quality, engineering, opex).
  • Experience in dealing with regulatory authorities such as FDA.
  • Managerial/leadership experience.

The base pay for this position is $ – $. In specific locations, the pay range may vary from the range posted.

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Position Requirements
10+ Years work experience
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