Systems Engineer, R&D - San Diego

Overview

Instrumentation Laboratory

Our Passion. Your Results.

Founded in 1959, Instrumentation Laboratory (IL) is a global leader in the development, manufacturing and distribution of diagnostic solutions for Acute Care Diagnostics, patient blood management and Hemostasis testing. Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We're passionate about providing medical professionals the most valuable and complete solutions to enhance patient care.

As an integral part of Werfen, a global healthcare company dedicated to delivering the highest quality in vitro diagnostic products, IL is supported by significant resources, outstanding scientific expertise and a tremendous knowledge base. IL is headquartered in Bedford, MA, USA.

Position Summary:

The System Engineer works with Accriva's development team by applying an interdisciplinary approach to the successful definition, development, integration, and testing of complex In Vitro Diagnostic systems.

The system engineer documents user requirements, develops system requirements, participates in product architecture and design, drives risk analysis, and supports integration and testing activities for both on-market products as well as new product introduction. The system engineer may have interactions with customers, clinicians, third-party vendors, manufacturers, and others

Responsibilities

  • Works with product management and marketing early in the development cycle to define & scope customer needs and required functionality.
  • Responsible for the development of the system requirements documentation.
  • Applies architectural & design skills to work with senior development engineers to decompose the System Requirements Documentation into a structured hierarchy of progressively smaller, but cohesive sub-systems and well defined interfaces.
  • Responsible for the creation of subsystem requirements documentation
  • Responsible for conducting and documenting hazard and risk analysis for projects
  • Develops system error budgets and conducts gage repeatability and reproducibility analysis
  • Supports design activities as needed, and attends design reviews
  • Manages continuous change, release & configuration management of the System, and it's sub systems and interfaces
  • Drives system integration, optimization, and root cause analysis with the development teams during system integration, Alpha testing, and device pre-Beta testing
  • Works with the testing teams to develop strategies for system level product integration and testing; including software, electrical, analytic, and mechanical aspects of the system
  • Supports the clinical teams as needed to ensure a structured approach to product validation
  • Creates work break down schedule estimates as needed
  • Operates electrical mechanical, digital equipment and test fixtures as needed
  • Works well in a team
  • Develops work products that reflect highly professional standards
  • Demonstrates excellent written and verbal communication skills
  • May provide leadership to a small team of engineers
  • May participate in interviews for new department personnel
  • May work on process improvement activities
  • Other duties as assigned with or without accommodation


Qualifications

  • BS/BA degree in CE, EE, ME, Biomedical or related Engineering discipline required
  • 3+ years industry experience
  • Experience in the product delivery to market of at least one product is desired
  • Experience in Medical device development or other Regulated industry is desired
  • Experience applying Six Sigma DMAIC as a means of improving, optimizing and stabilizing systems under development is desired
  • Experience applying DOE to systems under development is desired
  • Experience with UML is desired
  • Experience in application of Human Factors is desired


If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV.

Instrumentation Laboratory appreciates and values diversity. We are an Equal Opportunity/Affirmative Action Employer M/F/D/V

Werfen is a global leader in in vitro diagnostics (IVD) in the specialties of Hemostasis, Acute Care Diagnostics and Autoimmunity. Our core business is dedicated to R&D, manufacturing and distribution of diagnostic systems for hospitals and clinical laboratories. Our other areas of expertise include Original Equipment Manufacturing, Clinical Software, Clinical Chemistry, Infusion Therapy, and Medical Devices and Scientific Instrumentation Distribution.

We operate directly in over 30 countries and in more than 100 territories through distributors. In 2016, our turnover was approximately 1.2 billion euros and we had an average workforce of 4,400 people. Currently, we are over 5,000 employees.

www.instrumentationlaboratory.com/


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