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Jr. Validation and Verification Engineer 

EOE Statement We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law.  

Jr Software Validation and Verification Engineer

Position Description
This Software Validation and Verification Engineer assists with the software quality assurance efforts related to new product development and product modifications for the Research and Development group.

The position is responsible for ensuring that new products have been effectively and efficiently verified and validated before their shipment release. These designs meet documented and implied user needs and requirements. Software quality assurance efforts are lifecycle-oriented beginning during product requirements development and continuing throughout its lifetime.

This position will also be part of implementing software development tools to improve the overall quality of software, including peer reviews, software risk analysis, requirements traceability, defect tracking, configuration management, and software tool validations.

Primary Duties and Responsibilities

  • Develops test plans and protocols for proof of performance for medical devices.
  • Executes test plans and write reports to meet design control standards.
  • Extends plans and protocols as device features evolve.
  • Works closely with the software team to identify and correct defects that are found.
  • Performs risk analysis on software requirements and requested
    changes with the software team before the Implementation phase.
  • Communicates significant issues identified during validation activities and provides recommended process improvements to management.
Position Requirements

Education and Experience

  • BS in Software Engineering, Computer Science, or similar field.
  • Two years of related experience in validating software in an FDA regulated industry required.
  • Ability to interpret and analyze software programming languages,
    ???????preferably in C.
  • Must understand FDA software validation and life cycle requirements.

Skills and Competencies

  • Proven record developing and executing software test protocols for complex medical devices.
  • Experience in Software Risk Analysis with medical devices is strongly preferred.
  • Effective interpersonal communication skills and able to interface with cross-functional teams.


  • Strong technical writing skills; able to explain technical terminology in layman’s terms to Product Development groups, peers, and senior management.
  • Possess critical thinking skills and the ability to be assertive and challenge the process in a diplomatic manner.
  • Experience working with products from the prototype through 510(k)/ISO clearance and commercialization is preferred.
Full-Time/Part-Time Full-Time  
Position Senior Embedded Software Developer  
Location Palo Alto (HQ)  
About the Organization SCITON, a privately held and employee-owned company headquartered in Palo Alto, California, is a leading manufacturer of medical and aesthetic lasers and light source technologies. Founded by the laser industry's preeminent engineers and physicists, our mission is to provide best-in-class solutions to improve human conditions.

Our culture and company strength stems from our diverse collection of talented and motivated employees. One word that best describes Sciton is ‘Family' because we treat each team member like family. We give our employees the support, recognition, and room to grow their careers within Sciton.

We empower our people to develop their creative geniuses. In fact, we incentivize creativity and innovations to all our people. We look for lifelong learners, problem solvers, and individuals who excel in a challenging, team-oriented environment. We hire individuals who want to retire with us. How do you feel about that?


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