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Abbott
Abbott

Global healthcare company creating breakthrough diagnostics and devices

Quality Engineer lll at Abbott

RoleQA
LevelSenior
LocationCosta Rica - Alajuela
WorkOn-site
TypeFull-time
Posted1 day ago
Apply now

About the role

JOB DESCRIPTION:

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.
  • 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 Costa Rica – Alajuela location in the Structural Heart Division. 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 III, you will be responsible to work closely with Manufacturing and Engineering on sustaining activities to ensure compliance with the quality system requirements and achievement of Key Performance Indicators (i.e. NCMR’s, MA’s, Yield, Cost Reduction projects, etc.) and support/owns process/product validation activities.

Work closely with Research and Development and Regulatory Affairs personnel (internal or external) to obtained support on sustaining activities and during new product introduction to assure compliance with product and regulatory requirements.

Support of Major Quality System investigations (i.e. CAPAs, HHEs, Stop Ship, etc.) and audits (External / Internal).

What You’ll Do

  • Conduct technical and statistical investigations concerning optimization and compliance to specification.
  • Conduct NCMR Investigations, Calibration Out Of Tolerance (OOT) Investigations and Complaint Investigations (MA) related to manufacturing process.
  • Support/owns Major Quality System investigations (i.e. CAPAs, HHEs, Stop Ship, etc.) with minimum mentorship from higher level engineering.
  • Supports activities during preparation and execution of audits (External / Internal).
  • Executing and authoring IQ, OQ, PQ, and/or PPQ Qualifications and Inspection and Test Method Qualifications, typically with minimum mentorship from higher level engineering.
  • Perform supervisor activities to Quality Technicians, if required.

Required Qualifications

  • Bachelor´s Degree in STEM (Science, Technology, Engineering (preferred), Math) (with equivalent experience in medical devices or pharmaceutical quality control)
  • 2-4 years of experience in Quality or Engineering positions.
  • At least 2 years of experience in quality or manufacturing engineering roles.
  • Proficiency in computer applications (MS Excel, MS Word, MS PowerPoint).
  • Knowledge of statistical/data analysis and report writing experience.
  • Proficiency in computer applications (MS Excel, MS Word, MS PowerPoint).
  • Knowledge of statistical/data analysis and report writing experience.
  • Experience working on FDA, GMP, and ISO 13485 Regulated environments.
  • Experience in process improvement tools such as: Root Cause Analysis, Fishbone, Is/Is Not, Six Sigma or Process Control & Monitoring (SPC), Quality Tools.
  • Experience with control of nonconforming material, corrective and preventive actions as investigation owner and/or implementor.
  • Knowledge on product and process qualification and validation.
  • Intermediate command of English / Required
  • Capable of maintain fluent oral communication face to face or by conference.
  • Shift Administrative Preferred Qualifications
  • Experience with SAP.
  • ASQ CQE / Six Sigma or similar certification.
  • Participation or leading multi-department project teams.
  • Experience in supervision role.

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.

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

N/A

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

JOB FAMILY:

Operations Quality

DIVISION:

SH Structural Heart:

LOCATION:

Costa Rica > Alajuela : Parque Industrial, Zona Franca Coyol S.A Edificio #44B, Call0, Avendia 2

ADDITIONAL LOCATIONS:

WORK SHIFT:

Cr09Sal (Costa Rica)

TRAVEL:

No

MEDICAL SURVEILLANCE:

No

SIGNIFICANT WORK ACTIVITIES:

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous walking for prolonged periods (more than 2 hours at a time in an 8 hour day), Keyboard use (greater or equal to 50% of the workday), Work in a clean room environment

Required skills

Quality engineering

Process validation

CAPA

Quality systems

Root cause analysis

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About Abbott

Abbott

Abbott

Public

Abbott is a global healthcare company that develops medical devices, diagnostics, branded generic medicines, and nutrition products.

10,001+

Employees

Abbott Park

Headquarters

$177B

Valuation

Reviews

10 reviews

3.8

10 reviews

Work-life balance

3.2

Compensation

3.5

Culture

4.1

Career

3.4

Management

4.0

72%

Recommend to a friend

Pros

Supportive management and leadership

Good team culture and inclusive workplace

Excellent benefits and training programs

Cons

Heavy workload and overtime expectations

High stress and burnout potential

Limited advancement opportunities

Salary Ranges

754 data points

Junior/L3

Junior/L3 · IT ERP OCM - Data Analyst

1 reports

$82,383

total per year

Base

$71,594

Stock

-

Bonus

-

$82,383

$82,383

Interview experience

3 interviews

Difficulty

3.0

/ 5

Duration

14-28 weeks

Offer rate

33%

Experience

Positive 33%

Neutral 67%

Negative 0%

Interview process

1

Application Review

2

HR Screen

3

Technical Interview

4

Hiring Manager Interview

5

Offer

Common questions

Technical Knowledge

Behavioral/STAR

Past Experience

Problem Solving