SUMMARY:

The Principal Engineer / Program Manager is responsible for the execution of one or more simultaneous products under development. Leads and provides technical expertise to multi-departmental product development projects. Overall accountability for all program(s) cost, schedule and performance. Reports team progress and recommendations on a regular basis. Manages Company portfolio of programs as it relates to product development. Works with departments to ensure needs are incorporated in the development plans.

ESSENTIAL DUTIES & RESPONSIBILITIES (but are not limited to):

Project & Program Leadership

• Own full-cycle development project plans and deliverables.
• Track progress and milestones; develop recovery plans for deviations.

• Serve as the primary liaison to key stakeholders, providing timely updates on project milestones, risks, and progress.

• Lead core team meetings, setting clear goals and documenting outcomes.
• Apply appropriate project management techniques tailored to needs and risks.
• Resolve cross-functional barriers and delegate tasks across the team.
• Collaborate with functional managers to address resource constraints.

Technical Leadership & Execution

• Serve as a hands-on technical resource throughout the project.
• Perform investigational and early verification testing.
• Evaluate and resolve project issues impacting manufacturability and reliability.
• Engage with vendors for equipment, components, or services.
• Knowledge in the utilization of rapid prototyping, machine shop tools, and molding/extrusion methods.

Team Development & Culture

• Build and coordinate high-performing, collaborative teams.
• Foster accountability and clarity through strong communication and planning.
• Promote a team-first mindset aligned with organizational values.
• Mentor through example—emphasizing diligence, analysis, and goal-setting.

TECHNICAL SKILLS:

• Lead medical device product development as a technical lead or principal engineer
• Manage a cross-functional team through the product development life-cycle
• Serve as primary liaison to stakeholders, delivering timely updates regarding risks and milestones
• Knowledge of QSR CFR 820, ISO 13485, ISO 14971, and other applicable standards

CONCEPTUAL SKILLS:

• Self-starter with strong multitasking capabilities
• Creative problem-solver with sound judgment
• Detail-oriented with a focus on accuracy
• Skilled at prioritizing and maintaining focus on objectives
• Adaptable and solution-focused mindset
• Strong communicator across all levels
• Effective both independently and in cross-functional teams

EDUCATION / EXPERIENCE:

• Bachelor of Science Degree in Engineering (or similar) discipline.
• Minimum of ten years of previous engineering experience and minimum of seven years of project management experience in a regulated medical device environment.
• Education or experience in research & development, design, or process development.