- Location
- Taicang (Suzhou), China
- Type
- Full-time
- Department
- Engineering
- Education
- Bachelor
- Source
- Workday
Description
Job Title
Asist. Software Engineer
Location(s)
Taicang (Suzhou)About Us
Revvity is a developer and provider of end-to-end solutions designed to help scientists, researchers, and clinicians solve the world’s greatest health challenges. We pair the enthusiasm of an industry disruptor with the experience of a longtime leader. Our team of 11,000+ colleagues from around the globe are vital to our success and the reason we’re able to push boundaries in pursuit of better human health.
Find your future at Revvity
Key Responsibilities
- Assist in embedded software and upper computer software coding, debugging, function optimization and iterative upgrade for medical devices.
- Support software and hardware joint debugging, equipment function verification, data communication debugging and problem troubleshooting.
- Assist in software unit testing, integration testing, regression testing, record test data and track software defects.
- Complete standardized technical documents including software design documents, test reports and change records to meet medical compliance requirements.
- Participate in design verification and validation activities, and assist the quality team in medical system audit and product registration work.
- Responsible for daily software version management, file archiving and maintenance of full lifecycle traceability.
- Provide technical support for prototype trial production and mass production to ensure stable software operation of medical equipment.
Job Requirements
- Bachelor degree in Software Engineering, Computer Science, Electronic Engineering, Automation, Biomedical Engineering or related majors.
- Fresh graduates or 1–3 years relevant software development experience, medical device industry experience is preferred.
- Familiar with C / C++ / C# or other mainstream development languages, with basic embedded or PC software development capabilities.
- Understand basic software development processes; familiar with ISO 13485 and IEC 62304 medical standards is a plus.
- Familiar with Git version management, office software and basic data analysis.
- Strict and meticulous working attitude, good logical thinking, strong learning ability and team collaboration awareness.
- Able to standardize document writing and strictly implement medical product development and compliance management requirements.
Skills
GitCompliance