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Praxis Precision Medicines

Clinical-stage biopharma developing CNS therapies

Director Commercial Manufacturing Operations

Bioprocess & BiomanufacturingPosted on Nov 13
Full-timeRemote in USA$214k - $234k /yr

About the Job

Requirements

  • A bachelor's degree in engineering, pharmaceutical sciences, chemistry, or a related discipline is required; an advanced degree is preferred.
  • At least 15 years of pharmaceutical or biotechnology manufacturing experience, including significant leadership experience supporting commercial GMP operations.
  • Demonstrated experience leading manufacturing operations at a commercial manufacturing site as a Plant Manager, Operations Leader, or equivalent operational leader.
  • Significant experience managing external manufacturing partners (CDMOs) supporting commercial products.
  • Strong knowledge of commercial manufacturing operations, GMP regulations, quality systems, deviation management, CAPA processes, and continuous improvement methodologies.
  • Ability to influence cross-functional teams and external partners without direct reporting authority.
  • Ability to translate operational complexity into clear business decisions for senior leadership.
  • Ability to use a computer, devices, and office equipment regularly, communicate clearly, and perform occasional movement; comfort with screen work, basic hand coordination, and sustained focus is required. Reasonable accommodations may be made.

Responsibilities

  • Serve as the operational owner for commercial manufacturing performance at assigned CDMO partners, ensuring reliable execution of production schedules, supply commitments, and operational readiness.
  • Lead a cross-functional Virtual Manufacturing Team, aligning Manufacturing, MSAT, Quality, Supply Chain, Procurement, Regulatory, and Analytical Development around a common operational plan and clear priorities.
  • Develop operational visibility into manufacturing performance and proactively identify staffing, equipment, material, scheduling, and compliance risks before they affect patients or supply.
  • Establish performance metrics, monitor trends, and partner with CDMO leadership to improve right-first-time performance, schedule adherence, cycle times, yields, and manufacturing reliability.
  • Partner with Quality to ensure deviations, investigations, CAPAs, change controls, and audit observations are addressed promptly while maintaining GMP compliance.
  • Lead operational responses to manufacturing issues and act as the primary Praxis representative during batch-at-risk events, supply disruptions, or significant operational escalations.
  • Identify and implement continuous-improvement initiatives that improve operational performance, reduce cost, increase capacity, and strengthen long-term CDMO capabilities.

Desired Qualifications

  • An advanced degree.

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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