Staff Systems Test Engineer in Atlanta, GA, United States

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Staff Systems Test Engineer

Abbott Laboratories

  • Full_time
  • Industry : Medical Devices
  • image Atlanta, GA, United States
  • Zip Code : N/A
  • image November 17th 2017

Overview

Job description

At Abbott, we're committed to helping you live your best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world -- in nutrition, diagnostics, medical devices and branded generic pharmaceuticals -- that create more possibilities for more people at all stages of life. Today, 94,000 of us are working to help people live not just longer, but better, in the more than 150 countries we serve. Please note that candidates need to be eligible to work in the U.S. without Abbott sponsorship.

JOB DESCRIPTION:

Job Summary: Support product development efforts as a key member of program teams by leading verification and validation tasks and engineers for a smaller program or several features on a major program.
Job Duties:
Reviews and analyzes input requirements from a testability standpoint for new medical devices while supporting the instrumentation/service infrastructure.
Performs technical planning and performance evaluation studies, conducts technology assessment activities, analyzes system integration issues, •
Evaluates prototypes formally and informally through structured and ad hoc testing. Test aspects of new projects or algorithms to evaluate prototypes and validate output to meet intended use requirements.
Develops system verification and validation plans. Develops detailed test procedures for system level testing and sub-system verification, including software verification. Conducts and documents those tests.
Experience with Design Verification Test Method documentation and Test Method Validation
Experience with manual and automated tested, with ability to write SW code that drives automated tests
Ability to apply statistical analysis as related to sample sizes to be used for design verification
Evaluates, recommends, learns, trains about new verification and test tracing tools.
Identifies and resolves issues, escalating as appropriate.
Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
Performs other related duties and responsibilities, on occasion, as assigned.
Provides functional management and mentorship to small team of test engineers, including technician level and software verification engineers.
Qualifications:
Bachelor’s degree in software engineering, computer science, Biomedical Engineering or a related engineering field.
Typically a minimum of ten plus years of progressively more responsible work experience in a range of software engineering disciplines using a variety of programming methods
Training and experience in verification and validation processes, methods, and tools.
Demonstrated ability to apply an expert understanding of clinical application to issues in order to bring tasks to resolution within assigned projects.
Experience managing and mentoring other engineers
Medical device industry experience preferred.
Advanced credential in a relevant discipline/concentration, including Biomedical Engineering, 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.
Ability to travel approximately 5%, including internationally.
Ability to maintain regular and predictable attendance.
JOB FAMILY:
Product Development
DIVISION:
ASJM Abbott St. Jude Medical
LOCATION:
United States > Atlanta : 387 Technology Circle NW Suite 500
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Yes, 5 % of the Time
MEDICAL SURVEILLANCE:
Not Applicable
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: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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