Head of Engineering

About Us

iota Biosciences, a wholly owned subsidiary of Astellas Pharma US, is advancing a new class of bioelectronic medicines through the development of fully implantable Class III medical devices. Our proprietary technologies open therapeutic and diagnostic possibilities not previously accessible to clinicians.

We are currently focused on two programs : a first-of-its-kind neural interface which will transform recovery after stroke and pioneering direct bladder stimulation therapy for Underactive Bladder (UAB).

Together with Astellas, we are committed to patient-centric design, scientific and engineering excellence, and cross-functional teamwork. These principles guide us in bringing transformative, first-of-its-kind neurotechnologies into the clinic and closer to patients.

Role Overview

The Head of Engineering will report directly to the General Manager of the UAB program and serve as their key technical advisor. We are looking for a seasoned engineering leader to oversee and advance iota’s engineering and manufacturing functions from pivotal trials through pre-scale and into early commercialization . This leader will oversee all engineering and manufacturing functions, combining strategy, systems engineering expertise, and hands‑on leadership. Besides shaping the next‑generation platform and long‑term product strategy, you’ll influence how we optimize our technology, ensuring it not only meets regulatory milestones but also maximizes impact for patients.

What You’ll Do in This Role

Own the engineering strategy and broader R&D roadmap, guiding both the current clinical device and the next‑generation platform to ensure alignment with pivotal trial, PMA, and commercialization milestones

Lead and inspire a multidisciplinary team across electrical, software, firmware, mechanical engineering, and manufacturing engineering to deliver devices that are safe, reliable, and manufacturable at scale.

Oversee the transition from clinical builds to pre‑scaling and design transfer, owning supplier qualification, process validation, and readiness for commercial manufacturing.

Balance startup speed with Class III rigor, ensuring engineering decisions meet the highest regulatory standards without slowing innovation.

Roll up your sleeves to solve system‑level challenges, bringing deep technical expertise in how electrical, firmware, and mechanical components fit together, and guiding the team through complex systems integration decisions.

Key Responsibilities

Review, refine, and guide the engineering strategy to align with pivotal trial execution, PMA submission, and commercialization milestones, ensuring the team meets both short‑term and long‑term goals.

Own system architecture and integration across electrical, firmware, software and mechanical components, making informed trade‑offs that balance safety, reliability, cost, manufacturability, and clinical usability.

Establish and enforce robust design, design controls, reliability testing, and safety processes that meet or exceed FDA and international standards, including ISO 13485, IEC 60601, IEC 62304, ISO 10993, and ISO 14971, positioning the company for successful regulatory submissions.

Lead, mentor, and scale the engineering team, building technical depth while implementing processes that enable efficient execution, knowledge transfer, and readiness for organizational growth.

Partner closely with Clinical, Regulatory, Product Management, Quality, and Operations to deliver clinical builds, author and defend technical content for submissions, and strategic design transfer and pre‑scaling for commercial manufacturing.

Develop and own engineering budgets, resource planning, and timelines, ensuring visibility for leadership while proactively identifying risks and implementing mitigation strategies.

Must‑Have Qualifications

BS in Electrical Engineering, Systems Engineering, or related field.

12–15+ years of medical device experience.

Experience with Class III implantable devices through PMA approval and launch.

Deep systems engineering experience : architecture, integration, verification / validation.

Strong leadership skills with interest in mentoring early‑career engineers.

Experience working in a pre‑scale or growth‑stage company.

Nice‑to‑Have Qualifications

Experience with product lifecycle in medical device systems.

Global regulatory experience (CE / MDR).

Manufacturing scale‑up and cost‑of‑goods optimization.

Strategic thinker with hands‑on execution ability.

High integrity, adaptability, and ability to thrive in a startup environment.

Why Join Us

This is a rare opportunity to lead engineering at a pivotal stage — shaping technology strategy, mentoring a high‑performing team, and directly influencing the launch of a life‑changing implantable therapy. You’ll have the autonomy to define the engineering roadmap for next‑generation devices and the chance to build products that will change the lives of patients living with underactive bladder.

Benefits

Health & Wellness

Comprehensive health coverage for you and your family, covered at 100%

Access to quality dental and vision coverage

Onsite Gym in Alameda

Work‑Life Balance

Generous vacation pay

Paid parental leave

Options for flexible work schedules

Competitive Compensation

Annual Bonus Plan

Long Term Incentive Plan (LTIP)

401(k) plan with employer match

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