you will be an integral part of the design control process, working alongside a collaborative, multi-disciplinary team of software, electrical, mechanical, control, and systems engineers. You will be responsible for planning, executing, and documenting V V activities for complex electro-medical systems, ensuring compliance, performance, and safety across all phases of development. This is a hands-on role requiring technical depth, systems-level perspective, and cross-functional coordination.
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.