Associate Quality Engineer

Job Title

Associate Quality Engineer

About Abbott

Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.

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 will have access to:

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

• Health Insurance (starting on Day 1 of employment), Savings Plan (401K) with company match, Life insurance for you and your spouse/children, Short Term Disability, Long Term Disability, Education Assistance, Employee Assistance Program, Vacation, Sick, Personal Days.

• 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 Barceloneta location in the AV division at second shift. As a global leader in Medical Devices Technologies.

As the Associate Quality Engineer, you will provide Process/Quality Engineering support to manufacturing, helping to ensure delivery of highest quality product to the customer by assisting in the identification and resolution of quality related issues. The Associate Quality Engineer will work with line supervisor, manufacturing engineer, and other team members, to address all opportunities found in the assigned manufacturing line and will be the primary quality representative for the area.

What You’ll Do

• Responsible for compliance with applicable Corporate and Divisional Policies and procedures.

• Learns to identify Manufacturing process defects (scrap, nonconforming material, customer complaints) by disposition of non‐conforming material, assessing in identification of primary root causes and understanding corrective and preventive actions. May be responsible for working with process owner to bound product stops and document release criteria.

• Assists in development of product quality plans, documents and systems by providing input to product specification, quality specification, quality plans, risk analyses, FMEAs in conjunction with other product development team members. May be responsible for providing input to risk analyses and FMEAs.

• Learns Process Monitoring Systems by becoming familiar with systems applications and critical process steps; and through familiarization with methods used to reduce process variation.

• Becomes familiar with Product/Process improvement efforts by understanding current quality metric data and learning the various analysis methods used to enhance sustaining product design and new product development; learns Quality Tools & Training Materials by gaining knowledge of prevalent tools used and by reviewing & utilizing available training materials.

• Assist Product/Process improvement efforts (e.g). scrap, nonconforming product, customer complains) by systematically gathering quality metric data and by assessing in the appropriated analysis methods to enhance sustaining product design.

Required Qualifications

• Bachelor degree in Engineering.

• 0 - 2 years of related work experience with a basic understanding of specified functional area. Previous experience in medical devices or pharmaceutical industry is preferred.

• Bilingual. Fluent in English and Spanish.

Apply Now

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.