About the Role
In this role, you will play a critical part in ensuring the safety, functionality, and compliance of medical equipment used in patient care environments. You will work directly within hospitals and clinics, collaborating closely with biomedical teams and clinical staff.
Key Responsibilities
1. Perform on‑site inspections, checks, and technical verification of medical devices across hospitals and clinics
2. Ensure medical equipment operates safely and in compliance with local regulations, applicable standards, and hospital procedures
3. Conduct or support functional testing, safety testing, and preventive maintenance activities
4. Accurately document inspection results in maintenance or asset management systems
5. Collaborate with clinical staff, biomedical departments, and hospital management
6. Escalate identified technical issues and coordinate follow‑up actions or repairs as needed
7. Travel and work across multiple clinical sites, based on project requirements
What You Bring
8. Degree or qualification in Biomedical Engineering or Biomedical Engineering Technology
9. Minimum of 2 years of experience working with medical devices, preferably within hospitals or clinical environments
10. Alternatively, a background as an Electronics or Electrical Technician with relevant medical device experience
11. Hands‑on experience in medical device testing, inspection, servicing, or maintenance
12. Familiarity with medical device safety, quality, and compliance standards
13. Proficiency with MS Office and digital documentation or reporting tools
14. Ability to work independently, reliably, and efficiently in a project‑based setting
15. Strong communication skills with both technical and non‑technical stakeholders
16. Good English communication skills
17. Valid driving license, required for multi‑site hospital work
18. Own vehicle
19. Willingness to travel extensively within the country
Why Join This Project
20. Short‑ to mid‑term project with a clear scope and defined deliverables
21. Hands‑on work that directly contributes to patient safety and clinical quality
22. Flexible working arrangements (Full‑Time or Part‑Time)
23. Exposure to a variety of clinical environments, technologies, and medical devices
24. Structured project support within a professional and collaborative team environment
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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.