? Develop, write, and execute V V protocols and reports to validate product performance and
compliance with design requirements.
? Conduct hands-on testing of integrated hardware and software systems in lab and simulated clinical environments.
? Document and analyze TEST results, manage defect tracking, and prepare comprehensive TEST
reports.
? Lead and support root cause investigations and corrective actions, including regression testing.
? Collaborate closely with R D, Systems Engineering, and QA /RA to ensure product requirements are testable and risks are addressed through verification.
? Support and participate in external compliance testing (e.g., EMC, Safety, Environmental) conducted at certified laboratories.
? Participate in design reviews and ensure alignment with design controls, internal QMS procedures, and applicable standards.
Requirements: B.Sc. in Electrical, Mechanical, Biomedical Engineering, or a related technical field.
? Minimum 3 years of hands-on experience in a V V role within a medical device company.
? Strong experience in system -level testing of hardware/software products, including TEST protocol development and execution.
Preferred Qualifications:
? Experience working with energy-based aesthetic or therapeutic devices.
? Familiarity with regulatory testing requirements such as EMC, Safety, and Environmental standards.
? Ability to operate both independently and collaboratively within a cross-functional team
environment.
This position is open to all candidates.