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Praxis Precision Medicines

Clinical-stage biopharma developing CNS therapies

Principal Scientist - Process Chemistry

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeRemote in USA$165k - $185k /yr

About the Job

Requirements

  • An advanced degree or equivalent experience in Organic Chemistry, Pharmaceutical Sciences, Engineering, or a related discipline.
  • At least 5 years of industry experience in CMC specifically for small-molecule drug substance.
  • Strong knowledge of United States and European Union current Good Manufacturing Practice requirements and best practices relating to drug substances and drug products.
  • Strong knowledge of CMC development across all phases of drug development, from initial regulatory filings through registration, validation, and launch.
  • Experience working with third-party contract research organizations, contract manufacturing organizations, and associated service providers to develop and manufacture pharmaceutical products.
  • Interpersonal and communication skills to develop important relationships that include trust and encourage diversity.
  • Organization and attention to detail to deliver quality results.
  • Ability to meet the role's physical and mental requirements, including regular use of a computer and office equipment, clear communication, occasional movement, screen work, basic hand coordination, and focus; reasonable accommodations may be made.

Responsibilities

  • Lead Process Chemistry Research and Development for one or more projects from early to late phase.
  • Design early-phase and late-phase/commercial drug substance processes and lead their demonstration from the laboratory to the pilot plant.
  • Provide chemistry and technical leadership throughout the lifecycle.
  • Participate in or lead activities to identify final active pharmaceutical ingredient forms for pharmaceutical development.
  • Work with formulation, analytical, operations, engineering, and quality teams as part of the overall CMC team responsible for delivering clinical and commercial drug substance to company programs.
  • Identify, collaborate with, and lead external contract research organization and contract development and manufacturing organization partners to achieve deliverables.
  • Analyze external experimental data to guide synthetic experimental plans at contract research and manufacturing partners.
  • Author or co-author regulatory submissions.
  • Define manufacturing strategy and execution, including Good Manufacturing Practice requirements and issue resolution.
  • Assess and apply new trends and concerns in process development, quality, and manufacturing to company products.
  • Manage quarterly budgeting of drug-substance-related activities.
  • Contribute to inventions that add value to the company and its patients while strengthening its intellectual property position.

Desired Qualifications

  • Scientific track record or working knowledge in continuous processing, catalysis, biocatalysis, and/or high-throughput experimentation.
  • Experience with salt/crystalline form selection.
  • Experience with oligonucleotide chemistry.

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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