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Software Engineer (Instruments)

  • Salary: Negotiable
  • Job type: Permanent
  • Location: Limerick
  • Sector: IT
  • Date posted: 30/08/2018
  • Job reference: BBBH15558

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 to .

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