Principal System Integration Engineer - Transfusion and Transplant

Principal System Integration Engineer - Transfusion and Transplant

Job Summary

The Principal Systems Integration Engineer proactively leads and contributes to multiple moderate to complex projects and design changes in support of development and investigations. Responsible for developmental activities as well as design verification and validation related to products, assays, software and hardware.

• Identify testing plans for integration of new hardware components, assays, software, and products
• Lead efforts developing strategies for assay, software, hardware integration
• Lead team to evaluate/perform functional testing on new hardware/software/reagent
• Evaluate/perform functional testing on new analyzers and/or new configurations to support product development activities and make decisions towards defining parameters
• Design experiments using DOE methodology and analyze the test results using statistical tools. Interpret the results correctly and provide feedback effectively for design improvements.
• Perform advanced troubleshooting on automated systems
• Represent the Verification team on project core teams
• Perform statistical and verification data analysis at an advanced level
• Develop Verification Protocols to assure Requirements and Specifications are fulfilled
• Review results of executed Protocols and write summary reports and provide conclusions
• Anticipate the needs of the project and react to them accordingly without direction
• Perform traceability analysis of test protocol to Requirement
• Maintain adherence to PDP and GDP
• Write and execute moderately complex system related development and/or characterization protocols and data packages
• Review and approve verification and validation protocols and reports, as assigned
• Manage execution of verification and validation protocols
• Review technical risks and take appropriate action
• May assist in developing SHA and FMEA for Risk Management
• Support moderately complex investigations of system issues
• Presents, delivers and interprets information among product team members, scientists, engineers, and other systems development personnel
• Additional tasks assigned as needed to support ongoing integration projects related to product, assay, software and hardware

• Works closely with Systems Engineering, Quality, Regulatory, Assay Development, and occasionally Marketing and Clinical teams.

• Master's Degree (MA); or equivalent combination of education and experience
• Four to ten years of related work experience
• Experience in IVD development (software/system/assay focus) required
• Science or Engineering Degree Preferred

• Excellent written and verbal communication skills
• Excellent analysis, troubleshooting, and debugging skills
• Ability to perform in a fast‑paced, agile environment
• Ability to operate independently and exercise good judgment
• Understanding of technical content and the ability to communicate well with subject matter experts
• Works well with others in a collaborative, goal‑driven environment

• N/A

Mid‑Senior level

Full‑time

Quality Assurance

Medical Equipment Manufacturing