Scientist

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Job description

Job Title: Scientist
Location: Rochester, NY
Duration:24 Months+

Pay Range: $38/hr. on W2

Qualifications: 1-4 years' experience

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, Client (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 client 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

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