V V Lead to oversee and coordinate Verification Validation
activities for both software and hardware components in a regulated environment.
This full-time role offers the opportunity to work closely with multidisciplinary teams (R D, QA,
Operations) and contribute to the development of high-quality medical devices.
Key Responsibilities
Lead V V activities throughout the product lifecycle, from concept to release.
Develop and maintain V V documentation, including TEST Protocols, TEST Reports, and the V V
Master Plan.
Own and drive integration and system -level testing processes to ensure timely and effective
execution.
Requirements: Bachelors degree in Electrical Engineering, Software Engineering, Biomedical Engineering, or a
related technical field.
Minimum of 5 years of hands-on V V experience with complex software and hardware systems.
Proven experience with V V documentation and executing V V Master Plans.
Leadership experience with the ability to guide and support a V V team.
This position is open to all candidates.