Plano, Texas, United States
5 hours ago
Supplier Development Quality Engineer II

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.

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, 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 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 position works out of our Plano, TX location in the Neuromodulation Division. Our Neuromodulation business includes implantable devices compatible with mobile technology to help people who suffer from chronic pain and movement disorders. These non-opioid therapies allow us to provide interventional pain therapy to patients throughout the pain continuum.

Supplier Development Quality Engineers are responsible for activities related to supplier selection and evaluation, material qualification, supplier performance and receiving inspection. Supplier Development Quality Engineers drive improvement and corrective action in the quality of components sourced from outside suppliers. This position contributes to the development, establishment and maintenance of supplier quality engineering methodologies, systems and practices which meet Abbott and regulatory requirements. Each employee can make a difference at Abbott and has the power, either individually or as a team, to influence the success of the company. We are team-oriented, fast-paced and progressive. We value people with great ideas who partner with others both internally and externally to take action and accomplish goals.

What You’ll Work On

Assesses supplier capabilities through direct visits, technical discussions, directed testing and quality system auditsParticipate in supporting Supplier Development Quality program requirements (e.g., represent the Supplier Development Quality function as a Core Team Member)Reviews new design specifications and provides inputs for component quality and manufacturabilityMitigates risk by working with the Suppliers to document Process Flow Charts, PFMEAs, and Control PlansManages Supplier Change Requests, leading a cross-functional team.Reviews and approves supplied product drawings and component quality plansReviews and provides product inspection procedures and first article requirementsProvides engineering guidance to Abbott Receiving Inspection including statistical analysis, measurement techniques, Gage R&R studies and inspection proceduresProactively communicates quality issues to suppliers as needed through supplier quality system audits, supplier corrective action requests and technical discussionsContributes and participates in supplier performance reviewsWorks with Manufacturing engineering to assess and address purchased product issuesApply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issuesContributes to the development, maintenance and improvement of Abbott supplier quality program policies, procedures and formsComplies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignmentsMaintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendorsPerforms other related duties and responsibilities, on occasion, as assigned

Required Qualifications

Bachelor’s degree or equivalent experience and educationMinimum of 2 - 5 years of related work experience with a good understanding of the specified areaWorking technical knowledge and application of concepts, practices and proceduresGeneral understanding of business unit/group functionWill perform this job in a quality system environmentFailure to adequately perform tasks can result in noncompliance with governmental regulationsWorks on problems of moderate scope where analysis of situations or data requires a review of identifiable factorsExercises judgment within defined procedures and practices to determine appropriate actionHas a broad knowledge of technical alternatives and an understanding of their impact on the systems environment

Preferred Qualifications

Master's degree5 years of relative experience Previous Medical Device experience

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.



The base pay for this position is $60,000.00 – $120,000.00. In specific locations, the pay range may vary from the range posted.

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