Software Engineer (Instruments)

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Software Engineer (Instruments)

* Limerick

* Permanent

* Neg. Salary

My Client is a global medical technology company which specialise in devices, solutions and systems to address man of the world's most pressing healthcare needs.

Duties and responsibilities:

* Apply your software engineering prowess to development of complex electro/mechanical instruments.

* Innovate at all levels of our products, from instrument control, management and performance to new instrument applications and product security, all in collaboration with multidisciplinary teams.

* Be capable of working independently to specify, plan, design, develop, test and support software components; also presenting/participating in design reviews and code inspections

* Translate requirements into design and implementation of well-structured and documented software components; anticipate system faults, failures, or unusual events, ensuring software adequately mitigates identified risks, and develop automated unit test cases to assure software meets the design criteria

Qualifications include:

* BS degree in Computer Science, Computer Engineering, Electrical Engineering, Mathematics, Physics or other related engineering field with relevant experience in software development.

* Strong C# / .NET Development

* Strong C# / WinForms or WPF UI Development

* Experience with ADO.NET, Entity Framework or Nhiberate database interfacing tools

* A strong understanding of software design and systems & architecture concepts and their application in a professional environment within a software team structure.

* Understanding of software development lifecycle methodologies, including Agile.

Additionally, experience with the following would be a plus:

* Experience with electro/opto-mechanical instrumentation development

* Experience in Networking fundamentals

* Experience with software build and release process

* Interfaces to Laboratory Information Systems such as HL7 or ASTMKnowledge of international standards applicable to medical devices / risk management including ISO 60601-1, ISO 14971.

* Knowledge of software life cycle processes including IEC 62304

* Experience with data acquisition, analysis, and statistical methods.

* Demonstrated ability to comprehend and debug complex software systems

* Excellent written and oral communication and interpersonal skills are essential

* Experience working in a regulated (FDA) environment with medical instrumentation is a plus

* Experience in design verification of Medical Device in a FDA-regulated environment is preferred.

* Experience over the full product life cycle is desired

For more information or to apply to the role contact Emmet on 01 6455250 or email