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Praxis Precision Medicines

Clinical-stage biopharma developing CNS therapies

Director Combination Product Program Lead

Biomedical Engineering & Medical DevicesConfirmed live in the last 24 hours
Full-timeRemote in USA$205k - $225k /yr

About the Job

Requirements

  • Personally led the technical development of a drug-device combination product, including device design and engineering, verification and validation, human factors, and combination product risk management, with examples taken from early development through design transfer, submission, or launch.
  • Demonstrable experience taking devices or combination products through FDA regulatory processes, such as 21 CFR Part 4, design controls, or premarket submissions.
  • Background or experience in electrical engineering projects or a closely related area, with technical depth.
  • Working understanding of pharmaceuticals and medical devices, including combination product quality systems (ISO 13485), risk management (ISO 14971), human factors and usability engineering (IEC 62366), on-body and wearable delivery system requirements (ISO 11608, including Part 6), and medical electrical equipment safety (IEC 60601).
  • Evidence of leading people and programs while also delivering technical work personally.
  • Ability to coordinate specialists across functions and work with external partners and consultants.
  • Comfort and credibility presenting to and being challenged by senior leadership.

Responsibilities

  • Drive the drug-device combination program end to end, from device design and verification through risk management and design history file ownership; set strategy, build integrated timelines, manage risk, and maintain scope, quality, and deadlines.
  • Shape the FDA regulatory strategy for the combination product, coordinate device and drug considerations, and keep the program inspection-ready and submission-ready.
  • Translate between pharmaceutical development and device engineering so that both parts of the combination product advance in coordination.
  • Align and mobilize colleagues across scientific, regulatory, quality, clinical, and operations disciplines and seniority levels, without necessarily holding direct authority over all of them.
  • Serve as the day-to-day interface with the technology partner, ensuring collaboration, clear accountability, and shared momentum; direct and integrate external device and regulatory consultants.
  • Contribute hands-on technical problem-solving across electronics, software, electrochemistry, and delivery hardware.
  • Present progress, risks, and decisions to executive leadership.

Desired Qualifications

  • Hands-on strength in electronics and embedded hardware design.
  • Hands-on strength in software or firmware development.
  • Hands-on strength in electrochemistry applied to delivery or sensing.
  • Experience developing human implantable or body-worn devices.
  • Experience developing on-body, wearable, or transdermal delivery devices.
  • Direct end-to-end ownership of a combination product design history file, technical file, or design control documentation.

About the Company

Praxis Precision Medicines

Clinical-stage biopharma developing CNS therapies

Praxis Precision Medicines develops therapies for central nervous system disorders driven by neuronal imbalance, with a focus on genetic epilepsies. Its treatments target restoring balance in CNS networks and are advanced in clinical development to address unmet medical needs. The company differentiates itself by using patient-guided development and forming partnerships to align with real patient needs. Its goal is to bring effective CNS therapies to patients and caregivers by advancing through clinical development toward potential commercialization and collaborations.

Company size
201-500
Company stage
IPO
Headquarters
Cambridge, MA
Founded
2015

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