Skip to main content

Validation Engineer

BioProtectNetanya, Center District, IsraelNot specifiedFull-timeSeniority: Not specified

Posted 27 days ago · 48 applicants

Salary not listed for this role

Saving, applying or scoring takes a few seconds to set up your free account.

Willbi insight

The role in plain words

Must-have
  • B.Sc in Mechanical or Biotechnology or Biomedical Engineering
  • 2-5 years of experience in medical device company
  • Documenting and technical writing
  • Well organized and have a good eye for details
  • Good capability and understanding of machines and processes as well as the interface between the two
Nice-to-have

    Extracted from the job description · kept up to date automatically

    Who this suits

    Full job description

    Original listing · kept for reference

    We are looking for a Validation Engineer to join our team!

    Location: Netanya

    BioProtect Ltd is a leading medical startup in radiation protection technology. We offer spacers protecting healthy tissue during radiation oncology treatments, based on proprietary biodegradable balloon technology. The balloons suit a wide range of clinical applications in the fields of oncology and general surgery. The company’s first product, the BioProtect Balloon Implant, protects healthy tissue in patients undergoing radiation therapy for prostate cancer. Recently, BioProtect was acquired by Olympus Corporation and now operates as part of the Olympus Group.

    The opportunity:

    As a Validation Engineer, you will play a key role in the development of innovative medical devices for minimally invasive surgical and radiation oncology procedures. Working as part of a multidisciplinary R&D team, you will contribute to all stages of the product development lifecycle, from concept evaluation and design verification to validation and regulatory documentation. This is an exciting opportunity to combine hands-on engineering, technical problem-solving, and cross-functional collaboration while helping bring cutting-edge technologies to patients worldwide.

    In this position you will be asked to:

    • Identify and manage process improvement projects to optimize processes

    • Manage projects schedule

    • Perform Engineering product and process changes experiments

    • Perform and support validation and verification activities

    A successful candidate will have the following qualifications:

    • B.Sc in Mechanical or Biotechnology or Biomedical Engineering.

    • 2-5 years of experience in medical device company

    • Documenting and technical writing.

    • Well organized and have a good eye for details

    • Good capability and understanding of machines and processes as well as the interface between the two.

    • Excellent communication and interpersonal skills, include the ability to work independently as well as within a team.

    • Fluent English and Hebrew (written and verbal).

    BioProtect is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, colour, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

    About BioProtect
    Company profile · coming soon

    Employee reviews · coming soonMore roles at BioProtect

    Questions about this role

    • This listing did not state a salary. We only show pay when the employer publishes it.
    BioProtect
    Posted 27 days ago · 48 applicants
    See how you match