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This is where your work saves lives. As a part of Infusion Therapies & Platforms (ITP) division, the Senior Systems Verification Engineer, contributes to System Verification Engineering vision that aligns with the organization's vision and strategic plan. Use proven understanding of engineering theory and best-practice in a variety of fields to lead sophisticated projects or programs within boundaries of quality, time and budget. Exhibit creativity and innovation in completing divisional and cross-functional/business unit goals and objectives. Contribute to the plans and leads project assignments in the evaluation, selection and adaptation of various techniques, procedures, and criteria with minimal mentorship. Ensures that quality is built into the design during new product development.
Job Responsibility:
Contribute to the planning, development and execution of system verification deliverables (test plans, test protocols, test cases, test reports, studies)
Engage in test planning during design and development phases
Contribute to the validation efforts for laboratory equipment supporting infusion system testing
Develop and execute validation protocols, test plans, and reports in alignment with FDA, ISO, and equipment validation best practices
Perform IQ/OQ/PQ activities for lab equipment and ensure complete traceability from requirements through test execution
Contribute to the development and documentation of system requirements, systems architecture and design
Ensure appropriate traceability between system, subsystem, and software verification
Manage the integration of deliverables from subsystem teams, multi-functional teams and external partners
Resolve competing constraints between interrelated functions
Implement configuration and change management through the complete product life-cycle
Build process improvements to streamline testing between system verification, subsystem and software verification
Ensure all program achievements in support of all phases of the product development lifecycle are completed on time, with appropriate quality, and in compliance with relevant laboratory standards and regulations
Participate and/ or leads design reviews
Requirements:
Bachelor’s Degree in Mechanical, Electrical, Computer Science, Biomedical Engineering or equivalent
3+ years of relevant industry experience
Medical device industry experience is preferred
Proven organization skills and ability to collaborate with both technical and non-technical personnel
Solid understanding of ISO and/or FDA and other regulatory standards
Knowledge of Design controls, Lifecycle testing processes, MTBF analysis
Nice to have:
Medical device industry experience is preferred
What we offer:
medical and dental coverage that start on day one
insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP) with company matching
Flexible Spending Accounts
educational assistance programs
paid holidays
paid time off ranging from 20 to 35 days based on length of service