Program Manager

Location: Bedford, NH

Description: Our client is currently seeking a Program Manager

A leading medtech organization is seeking a Program Manager with deep medical device development experience to lead an active urology-based stimulator program. This role requires hands-on leadership in software development, cross-functional engineering coordination, and Agile program execution within a regulated environment.

About the Program

Software-driven urology stimulator device

Ongoing software development (team of ~4 developers, ~5 months remaining)

Verification team of ~3 engineers (~4 months)

Electrical engineering support (~1.5 resources for 2-3 months)

Internal resources already in place

Mid-maturity Agile environment in need of strengthened structure and discipline Key Responsibilities

Program Leadership

Lead a cross-functional medical device development program spanning software, verification, and electrical engineering.

Provide support and backup to Systems Engineering as needed.

Coordinate engineering resources to maintain alignment, momentum, and accountability.

Ensure program deliverables meet design control and medical device development requirements.Agile Execution (Scrum Master Responsibilities)

Break down epics into actionable user stories.

Facilitate sprint planning, backlog grooming, reviews, and retrospectives.

Track team velocity and enforce sprint discipline.

Drive consistent Agile practices within a regulated hybrid Agile-Waterfall framework.

Integrate Agile execution into the broader medical device lifecycle.Verification & Compliance

Coordinate execution of verification and validation (V&V) activities.

Maintain alignment with the organization's QMS and documentation processes.

Ensure proper handling of design control artifacts including requirements traceability, risk management, and verification protocols.Cross-Functional Coordination

Collaborate closely with software development, systems engineering, verification, and electrical teams.

Maintain program cadence and execution rigor across all functions.

Serve as the program's execution driver - not simply a status reporter. Required Qualifications

10+ years of medical device development experience

5+ years in Program Management

Strong background leading software-heavy medical device programs

Experience serving as a Scrum Master within regulated environments

Strong working knowledge of:

Medical Device QMS

Design Controls

Verification & Validation (V&V)

Requirements traceability

Engineering background preferred (Systems, Software, Electrical, etc.)

Experience running Agile within a Waterfall product lifecycle

Comfortable working in a mid-maturity Agile environment and able to enforce structure

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