As an Integration System Engineer in the Imaging Technologies team, you will own the end‑to‑end integration of a multidisciplinary medical device, from early design through validation and release.

You will lead system-level bring-up, define and execute integration strategies, and ensure robust interaction between mechanics, electronics, optics, and software.

This role emphasizes hands-on integration, performance analysis, and cross-functional alignment to deliver a high-quality, production-ready scanner.


Key Responsibilities

System Integration Ownership
Own system integration across all subsystems (mechanics, electronics, optics, software) and ensure a stable, testable, and scalable product.
Lead system bring-up, integration flows, and configuration management across development stages.
Identify interface gaps, define integration requirements, and drive closure with relevant teams.

Performance & Testing
Design and execute system-level experiments to evaluate performance, stability, and reliability.
Develop tools and automation for data collection, analysis, and debugging.
Define integration and verification test strategies, including acceptance criteria and coverage.

Problem Solving & Debug
Lead root-cause analysis of complex cross-domain issues.(HW/FW/SW/optics interactions).
Drive containment, corrective actions, and long-term fixes.
Ensure issues are resolved with clear documentation and learning capture.

Cross-Functional Leadership
Work closely with R&D disciplines, QA/RA, and manufacturing to align on system behavior and requirements.
Translate system-level needs into actionable specifications and integration plans.
Act as the technical focal point for integration-related decisions and trade-offs.

Process & Methodology
Establish and improve integration processes, methodologies, and best practices.
Introduce new tools, capabilities, and approaches to increase integration efficiency and quality.
Ensure proper documentation of integration flows, configurations, and test results.

Team Leadership & Mentorship
Mentor junior engineers and guide student contributors.
Assign and review tasks with a strong focus on quality, rigor, and engineering discipline.

We are seeking a highly motivated and experienced Production and Suppliers Quality Engineer to drive exceptional product quality, patient safety, and field reliability across the Installed Base (IB). This is a key technical role supporting production stability, RMA/DOA investigations, Automated Test Equipment (ATE) performance, and cross-functional quality engineering initiatives in a regulated medical device environment.

Key Responsibilities

In this role, you will:

Support qualifications and control of ATE testers in V&V phase and production lines.

Support ECO/ECR processes, NPI projects, product updates, and cross-functional engineering changes.

Participate in supplier selection and conduct suppliers audits.

Work closely with R&D, engineering, manufacturing, and operations teams to enhance product quality and resolve technical issues.

Drive continuous improvement initiatives using tools such as Six Sigma, Lean, and Root Cause Analysis (RCA).

Support RMA/DOA processes and continuous reduction of field failures.

Ensure compliance with ISO 13485, FDA 21 CFR 820, MDR, and other applicable medical device regulations.

Maintain and support quality documentation, including CAPA, Non-Conformance Reports (NCRs), and risk management documentation.