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.
Key Responsibilities
- 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.
Functie-eisen
- 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).
Competenties
- Attributes: High attention to detail with a strict "Quality-first" mindset; highly disciplined and accurate in technical documentation.
- Communication: Fluent in English (written and verbal); ability to confidently explain technical findings to various cross-functional stakeholders.
- Work Style: Ability to work autonomously, manage priorities, and maintain exceptionally high standards under project time pressures.
Arbeidsvoorwaarden
- Salary commensurate with your experience and expertise.
- 25 vacation days and 8% holiday allowance.
- Pension scheme starting from day one.
- Training budget and access to the Randstad Academy.
- Personal guidance from your dedicated consultant.
Uiteraard staat deze vacature open voor iedereen die zich hierin herkent.
contact
Ritika Agarwala
ritika.agarwala@randstadprofessional.nl
06-40981171
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