Founded in 1963, BIOTRONIK, Inc. is a pioneer in developing innovative technologies and medical devices that save and enhance the quality of life for millions of individuals living with cardiovascular disorders.   Our growing success is based on the company’s core values – innovation, excellence and reliability – thus enabling us to inspire confidence and trust in doctors and patients all over the world.  With a dedicated base of over 4,000 employees worldwide, we're continually looking for talented professionals with the passion and drive for excellence to join our mission.

Micro Systems Engineering, Inc., a wholly owned subsidiary of BIOTRONIK Gmbh., Inc., is now seeking an experienced and detail oriented professional for a Software Verification Engineer position in our dynamic and growing medical device manufacturing company.

This Software Verification Engineer position works primarily in testing software applications. The successful candidate will work on diverse issues, providing sound judgment within generally defined practices and policies.  He or she will work as part of a core team, as well as with cross-functional teams in other parts of the company, to ensure software quality and performance.

The Software Verification Engineer’s responsibilities include the following:

• Responsible for test design documentation, test code, and manual test procedures including significant test maintenance.
• Review documentation and code generated by other engineers.
• Execute tests to ensure conformance of code to requirements.
• Generate and maintain the appropriate work product deliverables from each phase of the verification.
• Review product design documents and programmer software.

Qualifications for the position include:

• BS/MS in Computer Science, Computer Engineering or Electrical Engineering is required.
• At least five years of software verification experience is required with considerable experience in creating and maintaining automated tests using at least one of the high level languages (C++ or C#).
• Experience working with configuration management, test management and defect tracking tools.
• Strong working knowledge of Microsoft Visual Studio and the .NET Framework.
• Experience with software lifecycle processes in a highly regulated environment (FDA, ISO) with a full understanding of best design practices.
• Experience with medical device software or experience in a regulated industry is preferred.
• Familiarity with Mercury Quality Center, Nunit, MKS Source Integrity, MKS Integrity Manager and Resharper are a plus.

For more information on BIOTRONIK, Inc. please visit our website at:

www.BIOTRONIK.com

For consideration, please APPLY NOW!