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The Respiratory and Monitoring Solutions Business Group is a $1.2
billion dollar division of Covidien, formerly Tyco Healthcare. RMS systems are
used to monitor, diagnose and treat respiratory disease and sleep disorders,
and provide life sustaining ventilation and oxygen support for patients. We
are currently recruiting for the following positions:
SOFTWARE QUALITY ENGINEER - Boulder, CO
Corp HQ – relo provided
Would
you -
Like to leverage your expertise in software
testing and with the software development process?
Move into software quality to help to set
up a more efficient and effective design processes?
Have a significant impact on product
quality?
Grow your
career and join a team that is working to get it right from the
start – refine the processes, redefine the activities, and make sure the proper
events occur at the right time?
Share your knowledge and support the
product design team providing guidance, mentoring and training?
Then join Covidien Respiratory and Monitoring
Solutions as a Software Quality Engineer!
Position Summary:
Responsible for ensuring that the
software used as part of our medical devices and products is developed according
to good design practices.
Minimum
Requirements:
BS EE, CS, or CE
3+ yrs in a
software quality engineering or software test role dealing with software that
is part of a medical device, or a product for a highly regulated industry i.e.
aerospace, automotive, etc. MED DEVICE NOT REQUIRED
Working
knowledge of product risk assessment, requirements management and tracing,
defect tracking, configuration management techniques, and how they are applied
in the software development lifecycle
Understanding
of current Software Quality techniques and software industry standards (e.g.
ISO, IEEE, CMMI), and their impact on internal procedures, software quality,
safety and efficacy of products
Working knowledge of C, C++, and
LabVIEW
SR. QUALITY ENGINEER - Boulder, CO Corp
HQ – relo provided
Position Summary:
Provide quality engineering support in the design and
development of medical device products, and facilitate the application of
design controls. Translate Quality
Standards into processes and procedures and apply these to the new product
design process.
Minimum Requirements:
BS in an engineering discipline, EE
preferred
5+ yrs of
quality engineering experience in a high volume manufacturing environment
Skilled in test plan development and root cause failure
analysis
Skilled in statistical methods,
including ANOVA, statistical process control, sampling plans, gauge R&R,
and design of experiments. Familiar with reliability analysis and test methods
Familiar
with ISO 14971 or strong experience in risk evaluation techniques, such as FMEA
and/or fault tree analysis
CQE certification desirable
For more
information about these opportunities, go to: www.covidien.com/careers. Pull up jobs for Boulder, CO
or send your resume to Tim.Wasik@Covidien.com
Covidien is an
Affirmative Action / Equal Opportunity Employer.
*Disclaimer: ASQ 1301 shall not be liable for the content or any errors or omissions in the information provided. Conclusions drawn from such information are the responsibility of the user.
Tracking code: 080626b
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