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Sr Systems Integration Test Engineer

Job in Goleta, Santa Barbara County, California, 93116, USA
Listing for: B. Braun Melsungen AG
Full Time position
Listed on 2026-06-28
Job specializations:
  • Manufacturing / Production
    Systems Engineer
Salary/Wage Range or Industry Benchmark: 100000 - 130000 USD Yearly USD 100000.00 130000.00 YEAR
Job Description & How to Apply Below

You’re an important part of our future. Hopefully, we're also a part of your future! At

B. Braun, we protect and improve the health of people worldwide. You support this vision, bringing expertise and sharing innovation, efficiency and sustainability as values. That’s why we would like to keep developing our company with you. Keeping your future in mind, we’re making a joint contribution to health care worldwide, with trust, transparency and appreciation. That's Sharing Expertise.

Company:
Digital Surgery Systems Inc.

Job Posting

Location:

Goleta, California, United States

Functional Area:

Information Technology

Working Model:
Onsite

Days of Work:
Friday, Thursday, Wednesday, Tuesday, Monday

Shift: 5X8

Relocation Available:
Yes

Requisition

B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nutrition, pharmacy admixture and compounding, ostomy and wound care, and dialysis. The company is committed to eliminating preventable treatment errors and enhancing patient, clinician and environmental safety.

B. Braun Medical is headquartered in Bethlehem, Pa., and is part of the

B. Braun Group of Companies in the U.S., which includes

B. Braun Interventional Systems, Aesculap®  True Digital Surgery and CAPS®.

True Digital Surgery, a

B. Braun company, is a World Leader in Computer‑Guided Microsurgery. We combine 3D visualization and guidance software applications focused on improving accuracy, efficiency and outcomes for surgeons and patients. Our medical imaging and guidance system employs advanced real‑time 3D graphic capabilities and proprietary software that is sold to surgeons and hospitals all over the world.

SUMMARY

The Senior Systems Integration & Test Engineer is responsible for helping shape future products as well as executing in the support of existing products. Ideally, they have experience integrating complex electro‑mechanical systems, specifically involving active robotics, high‑speed digital imaging, and precision optics. This role owns the formal verification process & strategy, leads iterative integration testing as the “tip of the spear” for sub‑system integration, and ensures the system performs reliably in a clinical environment.

The Senior Systems Integration and Test Engineer contributes to general systems engineering tasks, including requirements development, risk management (ISO 14971), and maintaining traceability throughout the design lifecycle.

ESSENTIAL DUTIES AND RESPONSIBILITIES
  • Lead the functional integration of hardware, software, firmware, and optical subsystems into a cohesive robotic microscope platform.
  • Develop and execute iterative testing and characterization experiments during early prototyping through system hardening to assess system performance and stability.
  • Characterize system performance with a focus on the intersection of features – such as opctical quality, robotic movement and computer vision.
  • Owner of Formal System Verification activities, including authoring protocols, executing formal runs, and generating reports. Coordinates other teams and resources assisting in Formal System Verification.
  • Review and collorabate to develop system‑level requirements, ensuring they are unambiguous, testable, and traceable.
  • Perform root cause analysis on complex system failures (hardware/software interactions) and drive defects to resolution
  • Design and build test fixtures, develop automated test scripts (Python, MATLAB, LABView),
  • Collaborate with Validation Team to validate that system meets the user needs of a surgeon in a clinical environment
  • Collarborate to ensure the traceability between system requirements and verification testing via Inputs Outputs Verification Validation (IOVV) matrix
  • Contribute to the system Risk Management File (RMF) via cross‑functional risk analysis, including DFMEA and UFMEA input
  • Support the regulatory submission process by ensuring all V&V data meets the standards for FDA and MDR compliance.
  • Participate in technical design reviews to provide “Design for Testability” feedback to the engineering team.
  • Review…
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