Abbott

Quality Engineer

Abbott$54K — $109K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in Engineering required.
  • Minimum 2 years of experience in Quality and/or Compliance, preferably in medical devices.
  • Knowledge of applicable US and non-US regulations.
  • Proficiency in Quality Engineering principles.
  • Bilingual: Excellent communication skills in English and Spanish.
  • Strong interpersonal skills to interact with all employee levels.
  • Proficient in Microsoft Office.

Responsibilities

  • Ensure compliance with Corporate and Divisional Policies.
  • Identify and resolve manufacturing process defects and non-conformance issues.
  • Support line teams to assess quality issues and manage exceptions.
  • Own and manage basic to moderate CAPA activities.
  • Conduct lot-to-lot yield evaluations and report quality metrics.
  • Contribute to product quality plans and documentation with a focus on risk analysis.
  • Lead continuous improvement efforts using quality metric data and analysis methods.

Benefits

  • On-site position in Caguas, Puerto Rico.
  • Participation in life-changing medical device initiatives.
  • Career development in a growing field focused on improving health quality.
  • Collaborative and supportive team environment.
Full Job Description

Quality Engineer. This position will support the Structural Heart business and will be based in Caguas, Puerto Rico.

On-site position.

The Opportunity

This position willprovide supportto our Medical Devices/Structural Heart business. Our medical devices help more than10,000 peoplehave healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than500,000 peoplewith diabetes from routinengersticks. 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 You27ll 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

  • Bachelor27s 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.

Apply now



The base pay for this position is

$54,300.00 6 $109,000.00

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

JOB FAMILY:Operations Quality

DIVISION:SH Structural Heart

LOCATION:Puerto Rico > Caguas : West Industrial Park Calle B, Lote #20

ADDITIONAL LOCATIONS:

WORK SHIFT:Standard

TRAVEL:Yes, 5 % of the Time

MEDICAL SURVEILLANCE:No

SIGNIFICANT WORK ACTIVITIES:Keyboard use (greater or equal to 50% of the workday)

About Abbott

Abbott Careers

Joining Abbott means becoming part of a globally diverse team dedicated to making a lasting impact on human health. As a leader in healthcare innovation, Abbott provides a dynamic workplace where careers flourish through growth, leadership, and diversity training.

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At Abbott, every role contributes to our mission of helping people live fuller lives through better health. From groundbreaking research in medical devices to advancements in pharmaceuticals, our team is at the forefront of healthcare innovation. By joining Abbott, you are not just accepting a job; you are embarking on a path of professional and personal growth.

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Our employees enjoy comprehensive benefits designed to support their life and well-being. From health insurance to retirement plans, we ensure our team has everything they need to thrive. Abbott's culture is built on a foundation of respect and integrity, united by a shared commitment to improving health outcomes.

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Explore Abbott

With a commitment to improving life through innovation, leadership, and diversity, Abbott is a place where you can fulfill your potential. See what exciting and rewarding opportunities await at Abbott by exploring our career opportunities today.

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Learn more about Abbott
Size
113,000 employees
Market Cap
$189 billion
Industry
Net Income
$4.4 billion
Founded
1944
5 Year Trend
+15.6%
Revenue
$34.6 billion
NASDAQ

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