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V&V Test Engineer (Validation & Verification) Job Opening In Bedford New Hampshire – Now Hiring Expert In Recruitment Solutions


Job description

V&V Test Engineer (Validation & Verification)

6 months+

Hybrid in Bedford, NH onsite 2 days a week (LOCAL ONLY NO RELO)





Looking for a versatile individual with deep skills and experience in medical device development to participate in product development, product verification and perform compliance activities.



Project: Verification and Validation work for Medical Device Company in Marlborough MA & Bedford, NH

  • Execute verification and validation testing of software and hardware for Class III medical device (high risk device aka ventilators, pacemakers, heart valves, etc)

  • Take requirement, review it for testability, write steps to test it, group the test steps into logical protocols, execute the protocol once approved and create the test record for the results

  • Update existing test protocols including hardware protocols that require knowledge of how to use an oscilloscope and then execute the tests and record the results

  • Systems level testing, mix of software and hardware




Responsibilities

  • This person will ramp up on system operation, supporting verification team, execute different verification test cases, work on the scope, develop scope, verifying

  • They will be working with the Test Leads for TIG device, as the Test Lead manages this and drives the workload.

  • Would be working with the Lead and a Software Engineer, providing feedback

  • The process is fixing and providing response, working on the features, then formal execution, software will then be complete then this person will officially test it and ensure operates as expected

  • They leverage DOORS (RQM) which is management tool and they draft test cases in,

  • This person will be looking at the requirement, executing that test cases and providing results


Profile:


  • 3-4 years experience with 1-2 roles medical device environment

  • Experience with writing verification procedures, execution and reporting on the verifications

  • Knowledge and understanding of medical device regulatory requirements (doesn't need EUMDR)





Required Skill Profession

Other General


  • Job Details

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