Quality Engineer.This position will support the Structural Heart business and will be based in Caguas, Puerto Rico.
On-site position.
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 will provide support to our Medical Devices / Structural Heart business. Our medical devices help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine ngersticks. Our business purpose is to restore health and improve quality of life through the design and provision of device and management solutions for the treatment of structural heart disease.
As the Quality Engineer 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.
This position will work the 1st shift.
What You’ll Do
Responsible for compliance with applicable Corporate and Divisional Policies and procedures.
Identifies manufacturing process defects (scrap, nonconforming material, customer complaints), dispositions non-conforming material, leads identification of primary root causes for basic investigations, identifies appropriate corrective and preventive actions.
Supports line support team (QC Supervisor, Mfg Supervisor, Quality Engineer and Operations) to perform line situation triage and determine if non-conformance is present, determine initial bracketing and containment, and initiate exception management process.
Owns basic to moderate exception / CAPA activities without oversight. May be responsible for working with process owner to bound product stops and document release criteria.
Can perform lot to lot yield and rework evaluation. May be responsible for reporting of quality metrics.
Understands product quality plans, documents, and quality systems.
Develops product quality plans, documents and systems by providing input to product specifications, quality specifications, quality plans, risk analyses, FMEAs in conjunction with other product development team members.
May be responsible for owning and maintaining product risk analyses and FMEAs. Monitors process by using process monitoring tools and Infinity QS 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.
Understands Quality Tools & Training Materials and helps others in gaining knowledge of prevalent tools used and available training materials.
Can lead Product/Process improvement efforts (e.g). scrap, nonconforming product, customer complains) by systematically gathering quality metric data and by using appropriate analysis methods to enhance sustaining product design.
Runs routine problem-solving investigation without oversight and use of six Sigma tools.
Implements minor and major changes through change management system and provides quality engineering impact assessment for changes implemented by other functional areas.
May write protocols and reports with management oversight to support engineering studies and validations.
Additional responsibilities may be:
May write protocols and reports with management oversight to support engineering studies and validations.
May write and /or approve protocols and reports with management oversight to support engineering studies and validations.
Required Qualifications
Bachelor's Degree, in Engineering.
Minimum 2 years of experience. Relevant experience in Quality and/or Compliance, preferably in medical device industry.
Knowledge of applicable US non-US applicable regulations.
Knowledge and proficiency in the application and principles of Quality Engineering.
Ability to effectively communicate cross-functionally to assist with resolving Quality issues.
Excellent written, verbal and interpersonal communication skills in both English and Spanish.
Ability to interact effectively with all levels of employees.
Digital skills. Microsoft Office.
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
$54,300.00 – $109,000.00In specific locations, the pay range may vary from the range posted.
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/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf
| Location | Caguas, Puerto Rico |
| Industry | Healthcare Services |
| Company Size | 10,000 employees or more |
| Year Founded | 1910 |
| Website | http://www.abbott.com/ |
At Abbott, we are enthusiastic, energetic and committed to doing great work every day. Our employees are passionate about helping to translate science into lasting contributions to health care and the health of people worldwide. At the heart of our organization is our "Promise for Life"—a statement that embodies our company's commitment to employees, shareholders, local communities and the people who depend on our company and products to live healthier lives.
Vital to our promise is the speed in which we act, respond and deliver. As Abbott employees, we are ready to meet change and challenges head-on. As a result, we are a company that adapts quickly, and through our passion for innovation we are able to continually create a pipeline of products that help improve the length and quality of life around the world.
We are proud of our rich, more than 120-year history. We continue to be driven to advance leading-edge science and technologies, support diversity, focus on exceptional performance and earn the trust of those we serve.
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