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On behalf of a global leader in life-saving medical technology, Randstad Digital is seeking a skilled EMC Test Engineer to join an independent, state-of-the-art Quality Laboratory (QLAB). In this critical role, you will ensure the safety of patients and healthcare workers worldwide by verifying that advanced medical devices comply with the latest international Electromagnetic Compatibility (EMC) standards. The QLAB is an IEC/ISO 17025 compliant facility and operates as a Customer Test Facility (CTF), assessed annually by global certifying agencies. You will join a dedicated, agile team where your expertise directly impacts the market release of cutting-edge healthcare products. With a wide variety of devices passing through the lab, your day-to-day work will remain dynamic, challenging, and highly impactful.
Job Responsibility
Test Execution & Analysis: Plan and perform EMC tests on hardware assemblies and final medical systems. Interpret complex EMC phenomena and analyze test results against international standards
Compliance & Documentation: Decide on "Pass/Fail" compliance based on strict performance criteria. Document technical observations with high detail and compile formal test reports for final product certification
Lab Management: Set up, maintain, and troubleshoot specialized test equipment and software. Manage a strict calibration regime and perform daily performance verification measurements
Quality Assurance: Operate within a rigorous Quality Management System (QMS). Promptly identify and report any non-conforming work to maintain the laboratory’s integrity and accreditation
Collaboration: Partner closely with a team of dedicated engineers, internal R&D development teams, and external certifying agencies
Requirements
Education: Bachelor’s (BSc) or Master’s (MSc) in Electronic Engineering, Electrical Engineering, or a closely related technical field
Experience: A minimum of 5 years of hands-on experience specifically in EMC Testing (experience within the medical device sector is highly preferred)
Regulatory Knowledge: Solid understanding of Quality Management Systems (QMS) and global regulatory frameworks (e.g., IEC, ISO, and medical device standards)
Nice to have
experience within the medical device sector is highly preferred