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Quality Engineer
Quality EngineerAbbott • Carlsbad, California, USA
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Quality Engineer

Quality Engineer

Abbott • Carlsbad, California, USA
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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 114000 colleagues serve people in more than 160 countries.

JOB DESCRIPTION : 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. Youll also have access to :

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

Employees can qualify forfree medical coverage in ourHealth Investment Plan (HIP) PPOmedical 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 bachelors 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 every day on site out of our Carlsbad CA location in the Cardiometabolic Division in Abbott Rapid Diagnostics. Our diagnostic solutions are used in hospitals laboratories and clinics around the globe. The crucial information derived from our tests instruments and informatics systems is often the first step in patient care decision-making for hundreds of health conditions from heart attacks to blood disorders to infectious diseases and cancers.

What Youll Work On

This position is responsible for developing and maintaining quality engineering methodologies and providing quality engineering support within new product development manufacturing or system / services support.

In addition :

Identify review and implement effective process control systems to support the development qualification and on-going manufacturing of products to meet or exceed internal and external requirements.

Perform Risk Assessments as required across functions including FMEA change management and issue investigation / resolution.

Lead in the review and / or implementation of assurances process controls and CAPA systems designed to meet or exceed internal and external requirements.

Assist in the review development and execution of streamlined business systems which effectively identify and resolve quality issues.

Apply sound systematic problem-solving methodologies in identifying prioritizing communicating and resolving quality issues.

Appropriately document experiment plans and results including protocol writing and reports.

Draft and review the CTQ parameters and specifications.

Lead the investigation resolution and prevention of product and process non-conformances.

Participate in or lead teams in supporting quality disciplines decisions and practices (e.g. represent the Quality function as a Core Team Member).

Requirements :

Required Qualifications

Bachelors degree in Science Engineering or a closely related discipline

More than 2 years Engineering experience and demonstrated use of Quality tools / methodologies.

Solid communication and interpersonal skills.

Project management and leadership skills including the demonstrated ability to lead multi-departmental project teams and resolve quality-related issues in a timely and effective manner.

Advanced computer skills including statistical / data analysis and report writing skills.

Prior medical device experience preferred.

Experience implementing various product and process improvement methodologies (e.g. Six Sigma and Lean Manufacturing). ASQ CQE or other certifications preferred.

Experience working in a broader enterprise / cross-division business unit model preferred. Ability to work in a highly matrixed and geographically diverse business environment.

Ability to work within a team and as an individual contributor in a fast-paced changing environment. Ability to leverage and / or engage others to accomplish projects.

Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization. Multitasks prioritizes and meets deadlines in timely manner.

Strong organizational and follow-up skills as well as attention to detail.

Preferred Qualifications :

Previous experience reviewing validation and transfer activities related to documentation control processes.

Americal Society of Quality (ASQ) and Certified Quality Engineer (CQE) or other certifications preferred.

Previous experience with Change management and Non-Conformance / CAPA.

Learn more about our health and wellness benefits which provide the security to help you and your family live full lives :

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 on Facebook at and on Twitter @AbbottNews.

The base pay for this position is

$79500.00 $138700.00

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

JOB FAMILY : Operations Quality

DIVISION :

CMI ARDx Cardiometabolic and Informatics

LOCATION : United States >

Carlsbad : 2251 Faraday Ave

ADDITIONAL LOCATIONS :

WORK SHIFT :

Standard

TRAVEL : Yes 5 % of the Time

MEDICAL SURVEILLANCE :

No

SIGNIFICANT WORK ACTIVITIES :

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day) Keyboard use (greater or equal to 50% of the workday)

Abbott is an Equal Opportunity Employer of Minorities / Women / Individuals with Disabilities / Protected Veterans.

EEO is the Law link - English :

EEO is the Law link - Espanol :

Key Skills

APQP,Quality Assurance,Six Sigma,ISO 9001,PPAP,Minitab,Root cause Analysis,ISO 13485,Quality Systems,Quality Management,As9100,Manufacturing

Employment Type : Full-Time

Experience : years

Vacancy : 1

Monthly Salary Salary : 79500 - 138700

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