Engineering Program Manager

Butterfly Network

6d•Hybrid

About The Position

We are seeking Customer Engineering Program Manager (EPM) to drive the execution of highly technical projects across engineering, manufacturing, and regulatory disciplines for Butterfly Embedded. The EPM will be responsible for program execution from concept to commercialization, ensuring that Octiv and its partners meet critical technical milestones while maintaining high efficiency. This role requires strong technical acumen, exceptional organizational skills, and experience leading complex projects in regulated environments.

Requirements

Bachelor’s or Master’s degree in Engineering, Computer Science, or a related field.
4+ years managing complex technical projects, preferably in hardware, semiconductors, or deep tech.
Proven track record of handling multiple projects and priorities.
Ability to translate technical challenges into actionable program management plans.
Familiarity with ISO 13485, FDA QSR, IEC 60601, or similar standards.
Proficient in project tracking, reporting, and analytics tools.
Experience coordinating work across hardware, software, and regulatory teams.

Nice To Haves

PMP, PgMP, or equivalent certification.
Experience with ultrasound or other medical imaging technologies.
Exposure to high-volume manufacturing environments.
Understanding of software development processes and integration workflows.

Responsibilities

Own the planning and execution of technical projects across the R&D, product development, new product introduction, and regulatory compliance.
Work closely with engineering, regulatory, quality, legal, and supply chain teams to ensure projects remain on track.
Track and manage project budgets, forecasts, and internal time tracking for accurate financial reporting.
Maintain alignment between Octiv’s technical priorities and those of its partners, ensuring deliverables meet strategic goals.
Keep detailed records of project milestones, technical dependencies, and risk management plans.
Work with internal and external teams to ensure medical device compliance, including FDA, ISO, and other regulatory standards.
Oversee procurement, production scheduling, and logistics to ensure timely delivery of products and components.
Identify bottlenecks in project execution and improve processes to enhance efficiency.