Join Our Team at Innoventric

We're always on the lookout for highly talented individuals who thrive
in a culture of teamwork, enthusiasm, and shared success. Explore how you
can be part of a dynamic team that values professionalism, collaboration, and the
power of collective innovation to make a lasting impact in medical technology.

We're always on the lookout for talented individuals who share our commitment to improving cardiac care. Explore how you can be part of a dynamic team that's setting new standards in medical technology.

R&D

V&V manager – Closed

Rehovot (On-site)

Full-time

Innoventric, a developer of transcatheter heart valves, is looking for an experienced Validation & Verification (V&V) Manager to lead and oversee the V&V and laboratory activities. The role requires strong background in V&V processes, experience in mechanical design, and a proven ability to comply with regulatory standards. As a key member of the R&D team, the V&V Manager will be responsible for driving high-quality testing, validation, and verification processes across multiple projects, ensuring that all products meet stringent safety and performance requirements.

Job Description:

Design, build, and maintain state-of-the-art test systems and run the mechanical laboratory.
Design and execute V&V protocols and test plans, ensuring compliance with regulatory requirements and industry standards (e.g., ISO, FDA).
Develop bench experimental systems (simulators, fatigue machines, tensile setups etc.)
Develop and implement test methods and procedures to assess device performance, reliability, and safety.
Participate in pre-clinical in-vivo experiments – including chronic follow-up and analysis of results.
Take an active role in designing a cardiovascular medical device and its supportive system components.
Analyze test data and generate comprehensive reports detailing findings, deviations, and recommendations for improvement.
Prepare and maintain detailed documentation for V&V activities, including test plans, protocols, reports, and risk management files.
Provide technical expertise and guidance on V&V issues throughout the product development lifecycle.

Job requirements:

Education: Bachelor’s or Master’s degree in Mechanical Engineering.
Experience: Minimum of 5 years experience in a medical device R&D team. Strong understanding of V&V methodologies and regulatory requirements (V&V role within cardiovascular – advantage).
Skills:
- Full control of SolidWorks.
- Proficiency in developing and executing V&V test plans and protocols.
- Experience with test equipment and statistical analysis methods.
- Strong orientation towards organized and well-documented work processes.
- Strong problem-solving skills, attention to detail, and mechanical orientation.
- Excellent communication and teamwork skills.
- Fluent in written and spoken English.

Working Environment:

Non-hybrid, Office and laboratory settings. Participation in pre-clinical trials. Occasional travel and participation in clinical procedures is required. Office – Rehovot/Ness Ziona science park.
Full-time position with standard office hours. Flexibility is needed to accommodate project deadlines.

Application Process:

Candidates who meet the job requirements are invited to send a CV to

ya**@in*********.com