Biomedical Engineer jobs in East Coast

Job Title: Calibration Engineer (Medical Devices | ISO/IEC 17025)

Employment Type:
Full-time

Industry:
Medical Devices / Precision Measurement /Quality Assurance

About the Role

We are seeking a meticulous and results-driven

Calibration Engineer

to join our technical operations team. In this role, you will be responsible for performing precise calibration, performance verification, and maintenance of medical devices and test equipment in strict compliance with

ISO/IEC 17025

and medical device regulatory standards.

You will play a critical role in ensuring measurement accuracy, technical competence, and data integrity to support our quality assurance and compliance goals.

Key Responsibilities

Calibration & Verification:
Perform technical calibration, testing, and troubleshooting for a range of medical equipment and calibration tools in accordance with established procedures and ISO/IEC 17025 standards.

ISO/IEC 17025 Compliance:
Maintain laboratory compliance, participate in accreditation assessments, maintain technical documentation, and calculate

Measurement Uncertainty (MU)

for test methods.

Metrological Traceability:
Ensure all reference standards and equipment maintain full metrological traceability to international standards (SI units).

Data Management & Documentation:
Prepare comprehensive calibration certificates, test reports, and technical documentation with high accuracy.

Quality & Corrective Actions:
Assist in investigating non-conformities, root-cause analyses, and implementing Corrective Action Plans (CAPA).

Equipment & Method Maintenance:
Participate in method validation/verification, inter-laboratory comparisons (ILC), and proficiency testing programs.

Requirements & Qualifications

Education:
Diploma or Bachelor’s Degree in Biomedical Engineering, Electrical Engineering, Applied Physics, or a related discipline.

Experience:
Minimum 2–3 years of hands-on experience in calibration or testing laboratories; prior experience in

Medical Devices

or an

ISO/IEC 17025-accredited

environment is highly preferred.

Technical Skills:
Solid understanding of metrological principles, measurement uncertainty evaluation, and equipment verification. Familiarity with medical device regulatory requirements (e.g., ISO 13485, HSA guidelines) is a plus.

Soft Skills:
Strong analytical problem-solving skills, sharp attention to detail, excellent organizational abilities, and strong written and verbal communication skills.

What We Offer

Competitive compensation package and performance bonuses.

Professional training and career advancement in medical device quality and accreditation.

A supportive, quality-focused working environment.

How to Apply

Interested candidates are invited to submit their updated resume detailing relevant experience and current/expected salary here.

Only shortlisted candidates will be notified.

Leedon was founded in Year 2002 by a group of experienced and dynamic professionals who have served in the Healthcare industry for many years. The group comprised of experts from various professions i.e. Nursing, Electronic and Biomedical Engineering, Fire and Security, IT and Hospital Building. Leedon is currently based in Singapore along with multiple associate companies around the region.

Leedon strives to be a solution provider to the Healthcare industry. It is our aim to provide manufacturers with a cost-effective, one-stop solution to market their product & equipment to the region.

Leedon has the networking capability to distribute the products, equipment and services around the Asian region. Leedon is accredited with ISO 17025 for our Rigel Service Centre handling medical tester and analyzer for the Regional Market and it is also the first accredited medical tester laboratory in Singapore. As part of our role as a marketer, Leedon has also attained the GDPMDS SS620:2016, BizSafe Level 4 and ISO 13485 certification.