Principal Process Engineer, Clinical Operations

Elucid•Boston, MA
•$135,000 - $165,000•Hybrid

About The Position

We are a rapidly growing, Boston-based medical technology company using AI to enable clinicians to make informed decisions on cardiovascular care - leading to better patient outcomes, improved quality of care, and reduced healthcare costs. Come work at Elucid and be part of delivering on our mission to prevent heart attacks and strokes! Are you passionate about driving operational efficiency in clinical production? Join us as a dynamic Principal Process Engineer to revolutionize our clinical production processes and build out workflows for our team of medical imaging analysts. In this pivotal role, you'll design and lead the operating model behind our team of expert image analysts, from the moment an image arrives to the moment results reach a clinician. You’ll set the metrics, build the workflows, and drive the handoffs with Clinical QA, SQA, Product, and Engineering that let us scale with confidence in an FDA-regulated environment. We’re looking for an experienced, hands-on process leader who pairs lean rigor with startup pragmatism and a background in medical imaging or medical devices. Your work will directly shape how our AI-enabled technology reaches patients as we rapidly commercialize.

Requirements

  • Bachelor's degree in Engineering, Biomedical Engineering, or a related field.
  • 8+ years of experience in process engineering or an operational optimization role with software-as-a-medical-device (SaMD) or medical imaging products.
  • Lean and/or Six Sigma experience.
  • Strong eye for optimization and a mindset of continuous improvement.
  • Excellent problem-solving and analytical skills.
  • Strong communication and collaboration abilities.
  • Detail-oriented, with a focus on quality and compliance.

Responsibilities

  • Design and lead the operating model behind a team of expert image analysts.
  • Set metrics for clinical production processes.
  • Build workflows for clinical production processes.
  • Drive handoffs with Clinical QA, SQA, Product, and Engineering.
  • Scale clinical production processes with confidence in an FDA-regulated environment.

Benefits

  • Flexible hybrid environment
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