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Open nowFirst seen 4 days ago

Verification & Validation (V&V) Manager

eitanmedical/c6.00f7 open roles

Where
Israel, Netanya
Work mode
On site
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Your applicationOpen nowVerification & Validation (V&V) Managereitanmedical/c6.00f · Israel, Netanya

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The clock on this job

Early applications get read.

12.3% of postings close within 7 days. Measured by our own scanner across the market. eitanmedical/c6.00f postings stay open a median of 1 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.3%7 days
  4. 19.3%14 days
  5. 35.6%30 days
  6. 57.8%60 days
This job: first seen 4 days ago

eitanmedical/c6.00f median: 1 days open

The posting

Eitan Medical is a fast-growing global medical device company that develops and manufactures innovative drug-delivery and infusion solutions across the continuum of care, from hospital to home. We are looking for an experienced V&V Manager to lead our V&V function and team within the R&D

Job Description

  • Lead the V&V function and define the verification and validation strategy for new products and design changes.
  • Manage, develop, and provide technical leadership to a multidisciplinary team of V&V engineers, including goal setting, workload allocation, mentoring, and performance development.
  • Ensure complete, risk-based test coverage and traceability from product and system requirements through test evidence and final reports.
  • Review and approve V&V plans, protocols, reports, deviations, and supporting technical documentation.
  • Oversee system-level hardware, software, mechanical, and disposable-set testing in the R&D laboratory and at external laboratories and subcontractors.
  • Lead experimental design, data analysis, structured problem-solving, and root-cause investigations.
  • Plan resources, equipment, schedules, and priorities, and monitor execution against project milestones and quality objectives.
  • Partner with Systems, R&D, Quality, Regulatory, Clinical, and Project Management teams, and provide V&V support during audits and regulatory submissions.

Reports to: R&D Director

Requirements

  • B.Sc. in Biomedical, Systems, Electrical, Mechanical, or a related engineering discipline.
  • At least 5 years of R&D experience in the medical-device industry, including at least 2 years of direct management experience leading technical or V&V staff.
  • Hands-on experience planning and leading system-level V&V for multidisciplinary medical devices combining hardware and software.
  • Strong knowledge of medical-device design controls, requirements traceability, risk-based V&V, and quality-system requirements.
  • Demonstrated experience developing, reviewing, and approving V&V strategies, plans, protocols, reports, and test deviations.
  • Strong leadership, project-management, analytical, and root-cause investigation skills.
  • Excellent cross-functional communication and stakeholder-management skills, with the ability to manage multiple priorities.
  • Fluent written and spoken English.

Advantages

  • Experience with infusion pumps, drug-delivery systems, or other active medical devices.
  • Working knowledge of relevant standards, such as ISO 13485, ISO 14971, IEC 60601-1, IEC 60601-1-2, IEC 62304, and IEC 62366-1.
  • Experience managing external laboratories and electrical safety, EMC, reliability, usability, or environmental testing.
  • Experience with sterilization validation process using EtO or radiation.
  • Experience with test automation, statistical analysis, or V&V performance metrics.
  • M.Sc. in Engineering or a related field.
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