Engineering team planning a medical device around a whiteboard of system diagrams
Capabilities · Program Leadership

Project Engineering

Program management and engineering leadership for medical and wellness device development — built for the realities of regulated product development. We drive your program, lead our team, and manage your outside vendors so you don't have to.

Most Projects Don't Fail. They Stall.

Medical and wellness device development rarely fails because of bad engineering. It stalls because no one is actively driving the program, coordinating disciplines, surfacing risks early, and making the next decision when something changes.

At C3, our project engineers do that work. They run the technical program, coordinate hardware, firmware, software, regulatory, manufacturing, and external vendors — and keep your device moving from concept toward production. With over 25 years of experience, we know where projects get stuck and how to keep them moving.

Program Leadership Capabilities.

Program planning, scheduling, and milestone management
Cross-discipline coordination across electronics, firmware, cloud, mobile, and V&V
Risk identification, tracking, and mitigation planning
Regulatory pathway planning and design history file management
ISO 13485 and IEC 62304 compliant development processes
Vendor and contract manufacturer coordination, including timeline management and technical communication on your behalf
Direct communication with your team and stakeholders

Where We've Run the Program.

Virtual Startup Wearable

C3 led development of a wearable medical device for a fully distributed startup with team members across the country. We integrated all internal and external contributors, brought the product through clinical trials, and held timeline and budget commitments across the entire program.

Mid-Size Life Sciences Workstation

A mid-size company needed to develop a complex life sciences workstation but didn't have the internal engineering capacity to drive it. C3 served as the engineering team and program lead, working alongside the client's internal resources — from planning and budgeting through end-product manufacturing test.

Enterprise Implantable Device

Large companies have full teams and large budgets, but they're often less nimble when fast turnarounds are needed. We've stepped in for major medical device companies to make urgent design additions and updates that their internal teams couldn't fit into their existing roadmaps.

A Simple Path Forward.

01
Start the Conversation

Talk directly with our team about your program, your timeline, and where things are getting stuck.

02
Get a Clear Plan

We define program scope, milestones, and the engineering disciplines needed — with project-based or retainer options that fit your stage.

03
Execute With Confidence

Our project engineers drive the program, manage vendors and contract manufacturers, and keep everything moving — while you focus on the strategic decisions only you can make.

What Working With C3 Looks Like.

Project engineer lead meeting directly with a client over a device and project notes
Direct Access to the People Driving the Work

You work directly with your project engineer lead — not a layer of account managers between you and the team.

Monitor displaying a detailed project timeline and Gantt chart with milestones for a medical-device program
Realistic Plans, Not Optimistic Ones

We commit to timelines we believe in. When risks emerge, we surface them early — not at the milestone review.

Hands arranging planning cards and annotating a printed product roadmap on a conference table
Built Around Your Stage

Startups, mid-size companies, and large enterprises all need different things from a project engineer. We adjust how we engage based on what your team actually needs.

How We Approach Project Engineering.

Plan, Then Lead

A good plan is just the start. Real program engineering means leading the work day-to-day: coordinating disciplines, managing vendors, removing blockers, and making the trade-offs that move the project forward.

Compliance From Day One

ISO 13485 and IEC 62304 compliant processes are part of how we work from the beginning — not something we retrofit before submission.

Transparent Communication

You always know where the project stands. No silent slippage, no surprises at the milestone review.

Ready to Move Your Program Forward?

Talk directly with our team about your program and get a clear plan for what comes next.