Junior Electronics Engineer (EMC/Safety)

Please note

• This is not a Software Testing Position
• We do not work with agencies.

Role Description

This is a full-time role (located in Erpe-Mere with the flexibility for some remote work) for a Junior Electronics Engineer (EMC/Safety). The Junior Electronics Engineer will be responsible for ensuring safe electrical and mechanical operation of medical devices in compliance with international medical regulations, analyzing and mitigating any electromagnetic interferences, and supporting product design teams in identifying and resolving potential design issues. The Junior Medical Engineer will collaborate with cross-functional teams, including R&D, Quality, and Regulatory Affairs, to ensure delivery of high quality, innovative, and regulatory compliant medical products.

Responsibilities

• Support the design and testing of electronic circuits and systems for medical devices, ensuring compliance with EMC and safety regulations.
• Collaborate with cross-functional teams to understand product requirements and integrate EMC/safety considerations into the design process from the outset.
• Assist in conducting EMC tests and safety evaluations, documenting results, and recommending improvements to meet international standards (e.g., IEC 60601-1, IEC 61000).
• Participate in risk assessments and FMEA sessions to identify potential EMC and safety issues, contributing to the development of mitigation strategies.
• Keep abreast of the latest developments in EMC standards, safety regulations, and best practices within the medical device industry.
• Work with senior engineers to develop and implement design changes that improve the EMC performance and safety of medical devices.

Qualifications

• Bachelor’s degree in Electrical Engineering, Electronics Engineering, or a related field, with a strong foundational knowledge in EMC and electronic safety principles.
• Familiarity with electronic design software (e.g., Altium Designer, Eagle) and EMC testing equipment.
• A basic understanding of the regulatory landscape for medical devices, particularly concerning electromagnetic compatibility and safety (knowledge of standards like IEC 60601-1 and IEC 61000 is a plus).
• Excellent problem-solving skills, with a meticulous approach to design and testing.
• Ability to work effectively in a team, contributing to collaborative problem-solving and project development.
• Eagerness to learn and adapt in a rapidly evolving field, with a commitment to professional growth and development in medical device engineering.
• Strong communication skills, capable of documenting and presenting findings and recommendations clearly and concisely.

At Qity, we are committed to the professional development of our team. The successful candidate will receive comprehensive training and support, gaining valuable skills and experience in various areas of medical device development and regulatory compliance.

If you have a passion for developing medical devices, an eagerness to learn, and a desire to work in a fast growing MedTech start-up, we encourage you to apply for this opportunity.