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Verification Validation Engineer

Job in Milpitas, Santa Clara County, California, 95035, USA
Listing for: Akkodis
Contract position
Listed on 2026-05-29
Job specializations:
  • Engineering
    Biomedical Engineer, Quality Engineering, Medical Device Industry, Validation Engineer
Salary/Wage Range or Industry Benchmark: 44 - 45 USD Hourly USD 44.00 45.00 HOUR
Job Description & How to Apply Below

Akkodis is seeking a Verification Validation Engineer for a contract job in Milpitas, CA United States, onsite.

Pay Range: $44/hr - $45/hr on W2

(The rate may be negotiable based on experience, education, geographic location, and other factors.)

Location:
Milpitas, CA United States, onsite.

Duration: 12 Month+(Possible to Extend)

Exp Required : 7 Years

Job Summary

We are seeking a detail-oriented and highly motivated Verification & Validation (V&V) Engineer to join our Medical Device Engineering team. The ideal candidate will be responsible for planning, executing, and documenting verification and validation activities to ensure medical devices meet design requirements, regulatory standards, and user needs.

Key Skills
  • Verification & Validation
  • Medical Device Testing
  • Design Controls
  • IQ/OQ/PQ
  • Regulatory Compliance
  • Documentation & Reporting
  • Cross-functional Collaboration
Role Description s
  • Experience in Medical Device industry (mandatory)
  • Develop and execute verification and validation protocols for medical devices and associated systems.
  • Review product requirements, specifications, and risk management files to create comprehensive test strategies.
  • Perform system, hardware, software, and usability testing activities.
  • Generate detailed test plans, test cases, traceability matrices, and validation reports.
  • Collaborate with cross-functional teams including R&D, Quality Assurance, Regulatory Affairs, Manufacturing, and Clinical teams.
  • Ensure compliance with FDA 21 CFR Part 820, ISO 13485, IEC 62304, IEC 60601, and other applicable standards.
  • Support design verification, process validation, and equipment qualification activities (IQ/OQ/PQ).
  • Investigate test failures, perform root cause analysis, and recommend corrective actions.
  • Maintain documentation in accordance with Design Control and Quality Management System requirements.
  • Participate in audits, inspections, and regulatory submissions as needed.
  • Contribute to continuous improvement of V&V processes and methodologies.
  • Strong experience with Validation & Verification (V&V) activities
  • Hands‑on experience in creating/executing test protocols and validation documentation
  • Understanding of quality and compliance standards within medical device environments
  • Familiarity with validation tools, defect tracking systems, and documentation management systems.
  • Experience working with Class II or Class III medical devices.

Equal Opportunity Employer / Veterans / Disabled

  • The California Fair Chance Act
  • Los Angeles City Fair Chance Ordinance
  • Los Angeles County Fair Chance Ordinance for Employers
Benefits

Benefit offerings available for our associates include medical, dental, vision, life insurance, short‑term disability, additional voluntary benefits, an EAP program, commuter benefits, and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.

Disclaimer:
These benefit offerings do not apply to client‑recruited jobs and jobs that are direct hires to a client.

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