Verification and Validation Engineer

"All candidates must be directly contracted by ASK Consulting on their payroll and cannot be subcontracted. We are unable to provide sponsorship at this moment".Job Title: Verification and Validation Engineer Location: Rochester , NY (Onsite) - locals onlyDuration: 12+ MonthsPay rate: $38/hrJob Description:Basic Qualifications for Consideration:Qualifications (skills, knowledge & abilities):Must be a resident of the Rochester, NY area or be willing to commute daily to work fulltime onsite, no WFHStrong written and verbal skills; confident/comfortable making presentations to othersExcellent problem-solving and trouble-shooting skills, requires some initiative and judgmentExcellent organizational skills and attention to detailsAbility to work within constraints as well as to challenge constraints to support good designFamiliar with design and requirements engineering for medical devicesFamiliar with applicable development processesFamiliar with general laboratory equipment and proper operation of such following SOPsTechnical ability to understand the mechanical, electrical and software components of a systemAbility to carry out general biochemical laboratory procedures including handling of human blood/serum samples and reagents for testing purposesKnowledge of development environment tools like Serena Business Mashups, HP (ALM) Quality Center, Aligned Elements, and Microsoft Team Foundation Server a plusExperience with Jira, Windchill and Quality Center a plusThese qualifications are typically associated with a minimum education of Bachelors Systems Engineering, Mechanical Engineering, Electrical Engineering or equivalent. Experience with any analyzers - especially family of Vitros Systems is a plus.Responsibilities:Major Job Functions:Perform hardware verification and validation testing, independently and/or, on multi-disciplined teams throughout the equipment/instrument development life cycle process. Apply system engineering methods for design and analysis, design verification, subsystem validation, and post launch product support.Work independently and as a team member to plan, write, and execute test cases according to Quality Management System, FDA regulations, and ISO standardsDesign new test procedures for new features and functionalityDevelop self and always maintain knowledge in hardware test engineering fieldParticipate in the execution, analysis, and reporting of subsystem and system testingWillingness to work in FDA/EU regulated medical devices environment utilizing defined processes and best practicesDevelop and execute verification and validation activitiesExecute test procedures, record, and later follow-up anomalies found during testingCommunicate Test development and Execution status to Team LeaderPerform other duties and projects as assignedAbout ASKASK Consulting is an award-winning technology and professional services recruiting firm servicing Fortune 500 organizations nationally. With 5 nationwide offices, two global delivery centers, and employees in 42 states-ASK Consulting connects people with amazing opportunitiesASK Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all associates.

Created: 2024-11-15