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 Associate Software Engineer

Details
Country: USA
Location: Massachusetts-Boston North Burlington, MA 01803
Total applied: 2
Salary/Wage:Competitive compensation
Job Category:IT/Software Development
Relevant Work Experience:2+ to 5 Years
Education Level:Bachelor's Degree
Location:Burlington, MA 01803
Status:Full Time, Employee
Occupations:Database Development/Administration;General/Other: IT/Software Development;Software/System Architecture
Career Level:Experienced (Non-Manager)
Relevant Work Experience:2+ to 5 Years
Associate Software Engineer

Associate Software Engineer About Us

CorNova is a medical device company headquartered in Burlington, MA with offices in Munich, Germany and Buenos Aires, Argentina. We are focused on developing next-generation endovascular products. These products include breakthrough technologies in advanced materials, coatings, cardiovascular diagnostics, and treatments designed to revolutionize the field of interventional medicine. If you are looking to work in a dynamic environment where you can make a difference this could be the place for you.Job Description:

We are looking to hire a Software Engineer for our Burlington, Massachusetts facility. The ideal candidate will be a team player who enjoys a fast paced environment which is both challenging and rewarding. The ideal candidate will have experience developing software systems and have innovative and timely solution approaches to problem solving.

 

Preferred Skills or Qualifications: BS degree from an accredited Computer Science/Engineering program 2-5 years of related experience with a minimum of 2 years of experience working in open source software development environments. Must have strong analytical and problem solving skills, as well as an understanding of the product development process. Embedded Linux experience is desirable. Device driver experience preferred.

 

Job Tasks and Responsibilities: Work closely with other engineers, technicians, contract manufacturers, assemblers, or other support personnel to assist in debugging and optimizing the system performance. Work with minimal supervision and strong initiative and execute project work and objectives with technical and creative proficiency. Perform design, development and process related engineering duties in the development of new medical products and devices. Responsible for performing design reviews and pre-validation assessments to ensure the safe and environmentally sound start-up of new processes.Benefits: Competitive compensation Great benefits package including paid time off (vacation), holidays, and medical/dental/life insurances 401k plan with matching

 

Principals only, please. This company does not offer relocation assistance. We are an equal opportunity employer, M/F/D/V.

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