招聘
Compensation
$81,500 - $141,300
Required Skills
Quality Assurance
Software Quality Engineering
FDA QSR
ISO13485
ISO14971
IEC62304
Computer Systems Validation
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 114,000 colleagues serve people in more than 160 countries.
JOB DESCRIPTION:
The Opportunity:
This
Nonproduct SW Quality Engineer is responsible for ensuring that computerized systems used in the support of the Quality System are developed, validated and maintained in compliance with regulatory and corporate requirements. They help to organize and maintain an inventory of software computerized systems and tools in use to ensure they are in a continued state of validation. They are a key contributor to validation efforts by reviewing quality system documentation as they apply to the development, verification, validation, use, and maintenance of the software or firmware. They independently coordinate activities with other functions and departments to complete validation activities and to see projects through to completion.
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What You’ll Work On
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Provides Quality guidance in direct support of implementation and maintenance of the nonproduct software lifecycles.
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Contributes to multiple portions of the Quality System, including but not limited to Master Validation Plans, Impact Assessments, Validation Plans, System Specifications, Requirements, Test Protocols, Test Reports, Trace Matrices, Summary reports, NC/CAPA, and others as needed.
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Develops and conducts training of company personnel for the divisional non-product software development and validation program
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Completes SWQA tasks in accordance with current Quality System Requirements.
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Works independently with objectives given by manager, planning and coordinating own work to high-level project schedules
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Reviews pre-defined deliverables/activities as identified in the SWQA Non-Product Quality Process, Company Policies, or project plans.
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Reports unexpected events, issues or software bugs which occur during verification/validation to project team and management.
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Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating and resolving issues.
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Develops and maintains departmental operating procedures to ensure compliance to relevant FDA QSR, ISO guidelines, including 21 CFR Part 11 and Abbott Corporate requirements as they relate to the development, verification, validation and maintenance of computerized systems used in the Quality System as well as those used in the development of ADC software/firmware products.
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Ensures that appropriate procedures, controls, and disaster recovery plans are incorporated into new computerized systems.
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Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
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Required Qualifications
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Bachelor’s Degree, preferably in Engineering, Technical Field, Life Science, or related discipline or an equivalent combination of education and work experience.
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2+ years’ experience in a Quality Assurance or software quality engineering experience in a medical device company
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Knowledge of FDA QSR, ISO13485, ISO14971, IEC62304 and FDA Computer Systems Validation (CSV).
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Preferred Qualifications
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Knowledge of Jira, Confluence, ALM Quality Center, and/or other software development and test tools is a plus.
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ASQ Certifications a plus.
The base pay for this position is
$81,500.00 – $141,300.00
In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Operations Quality
DIVISION:
LNGO Lingo
LOCATION:
United States > Alameda : 2901 Harbor Bay Parkway
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), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
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EEO is the Law link
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English: http://webstorage.abbott.com/common/External/EEO_English.pdf
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EEO is the Law link
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Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf
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About Abbott

Abbott
PublicAbbott is a global healthcare company that develops medical devices, diagnostics, branded generic medicines, and nutrition products.
10,001+
Employees
Abbott Park
Headquarters
Reviews
3.4
10 reviews
Work Life Balance
2.5
Compensation
4.0
Culture
2.8
Career
3.2
Management
2.5
45%
Recommend to a Friend
Pros
Good benefits and compensation
Supportive management/teams
Good company reputation and mission
Cons
Poor management and communication
Stressful work environment
Limited career advancement/favoritism
Salary Ranges
1,330 data points
Mid/L4
Mid/L4 · Clinical Specialist
192 reports
$122,947
total / year
Base
$107,979
Stock
-
Bonus
$14,968
$82,590
$185,149
Interview Experience
3 interviews
Difficulty
2.7
/ 5
Duration
14-28 weeks
Offer Rate
67%
Experience
Positive 67%
Neutral 33%
Negative 0%
Interview Process
1
Application Review
2
Recruiter Screen
3
Phone Screen
4
Hiring Manager Interview
5
In-person/Final Interview
6
Offer
Common Questions
Technical Knowledge
Behavioral/STAR
Past Experience
Culture Fit
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