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.
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.
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