Director, Product Engineering

ABOUT ORGANOX

Organ Ox is an innovative, fast‑paced, global medical device company with a mission to save lives by making every donated organ count. We are a commercial stage organ technology company, spun out of the University of Oxford in 2008, committed to improving transplantation outcomes throughout the world. The company’s first product, the Organ Oxmetra® normothermic machine perfusion (NMP) system for liver transplantation, has been used to support more than 5,000 liver transplant operations globally.

The Engineering Director – Product Engineering position oversees project management and addresses supply and design‑related matters for the released portfolio of Organ Ox Normothermic Machine Perfusion (NMP) products, currently the ‘metra’. The metra device is a medical system integrating multiple engineering disciplines, utilizing both capital equipment and disposable components to support liver transplants and improve organ availability.

Responsibilities include developing new features within the lifecycle management of the current product range. This role involves leading cross‑functional teams to identify issues, develop corrective action plans, and implement solutions related to both technical product matters and broader product development challenges. This position requires interaction with upper management for project reporting and phase reviews. The role encompasses experience with various therapies, products, and operational considerations connected to patient care and business objectives.

This is a full‑time role in Madison, NJ, with extensive collaboration with colleagues based in Oxford, UK.

• Lead cross‑functional team members to ensure clear communication and coordination of project/program objectives, deliverables, and timing of key milestones.
• Orient quickly to understand new quality issues based on field or factory performance, and to concurrently manage multiple projects with different teams while balancing competing priorities.
• May take direct responsibility for design‑related CAPAs (Corrective and Preventive Action) within the Product Engineering department as well as process‑focused CAPAs.
• Author investigation (i.e., root‑cause analysis) plans, reports, and supporting documents of high quality (i.e., submission and audit/inspection ready) that are technically sound, critically reasoned, and use appropriate root‑cause tools/methodologies (e.g., 5‑Whys/Cause Map, Contradiction Matrix, other DRM/Six Sigma problem‑solving and statistical analyses).
• Provide clear and concise communication – both written and verbal. Author strong documentation with attention‑to‑detail that is audit‑ready. Present team’s investigation findings and action recommendations to quality (e.g., CAPA Board) and other management/business stakeholders.
• Plan schedule and resources (e.g., labor skills sets and duration, expenses) to achieve desired project outcomes.
• Responsible for maintaining a focus on quality, while effectively partnering with Quality, R&D, Operations, and Regulatory stakeholders to facilitate consensus, resolve disagreements, and ensure sound decision‑making.
• Adhere to the letter and spirit of Organ Ox’s Code of Conduct and all other company policies.

• Experience in medical device or highly regulated industry.
• Experience or technical education in software development, software or computer engineering, and/or software quality assurance, including knowledge of IEC 62304 (Medical device software – software life cycle processes).
• Experience with medical device systems that include software applications and/or embedded software (i.e., firmware).
• Experience leading a complex project/program including cross‑functional team leadership, risk‑based decision making, financial accountability, and ability to manage change implementation.
• Background with CAPA (Corrective and Preventive Action) process, and/or experience with the use of root‑cause investigation, problem‑solving, or similar structured methodologies and tools (e.g., 5‑Whys, Fishbone, etc.).
• Experience participating in or supporting audits or external inspections (e.g., FDA, TUV, internal…