R&D Software Development Engineer

2 months ago

Singapur, Singapore BIOTRONIK Full time
R&D Engineer II (Software Development)

BIOTRONIK, a leading manufacturer of cardio- and endovascular medical devices, is seeking a highly skilled R&D Engineer II (Software Development) to join its global workforce. As a key member of the R&D team, you will be responsible for designing, developing, maintaining, and improving automated machines and test equipment, including integration with middleware and MES.

Key Responsibilities:
  • Design and implement equipment control/test software as part of agile teams.
  • Develop end-to-end automated machine, middleware, and MES integration/verification.
  • Maintain and enhance automated test frameworks, tools, and testers.
  • Document requirements and coordinate enhancements in assigned areas.
  • Lead and/or participate in cross-functional teams to support development/test projects.
  • Document test system and software designs.
  • Implement test plans, procedures, and generate reports.
  • Perform verification and validation testing.
  • Interpret requirements, identify design parameters, and ensure solutions are implemented accurately and within budget.
  • Develop new manufacturing processes with a focus on automation for new product development activities.
Requirements:
  • Masters/bachelor's degree in Electrical or Electronics/Communication Engineering with 5 years' experience in Software Development.
  • Experience in writing verification plans, test cases, defects reports, executing, and managing test cases.
  • Software test development experience with programming and scripting languages (C#, Type Script, shell script preferred).
  • Strong technical ability and knowledge of test instrumentation devices such as signal generators, oscilloscopes, spectrum analyzers, and power meters.
  • Advanced understanding of statistical data analysis, design margin principles, analog and digital measurement techniques, schematic capture skills, and manufacturing processes.
  • Familiar with serial communication protocols and hardware – CAN, SPI, Ethernet, HERMES.
  • Familiar with SMEMA/SECS/GEM/OPC-UA.
  • Familiar with continuous testing and related tools such as Jenkins or GitHub.
  • In-depth working experience in CE/FDA regulated industries will be an advantage.
  • Experience in high-volume, high-tech manufacturing environments.
  • Experience working within a quality and design-controlled environment (ISO 13485/GMP) will be an advantage.
  • Expertise in the development of medical products and approval process is preferred.
  • Project Management Experience preferred.
  • Ability to demonstrate time management skills.
  • Team player with strong organizational, interpersonal, communication, and intercultural skills.
What We Offer:
  • Opportunities to think and act entrepreneurially.
  • Working in global teams and projects.
  • Developing yourself professionally.

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