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 only
Duration: 12+ Months
Pay rate: $38/hr
Job 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 WFH
- Strong written and verbal skills; confident/comfortable making presentations to others
- Excellent problem-solving and trouble-shooting skills, requires some initiative and judgment
- Excellent organizational skills and attention to details
- Ability to work within constraints as well as to challenge constraints to support good design
- Familiar with design and requirements engineering for medical devices
- Familiar with applicable development processes
- Familiar with general laboratory equipment and proper operation of such following SOPs
- Technical ability to understand the mechanical, electrical and software components of a system
- Ability to carry out general biochemical laboratory procedures including handling of human blood/serum samples and reagents for testing purposes
- Knowledge of development environment tools like Serena Business Mashups, HP (ALM) Quality Center, Aligned Elements, and Microsoft Team Foundation Server a plus
- Experience with Jira, Windchill and Quality Center a plus
- These 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 standards
- Design new test procedures for new features and functionality
- Develop self and always maintain knowledge in hardware test engineering field
- Participate in the execution, analysis, and reporting of subsystem and system testing
- Willingness to work in FDA/EU regulated medical devices environment utilizing defined processes and best practices
- Develop and execute verification and validation activities
- Execute test procedures, record, and later follow-up anomalies found during testing
- Communicate Test development and Execution status to Team Leader
- Perform other duties and projects as assigned
About ASK: ASK 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 opportunities
ASK Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all associates.