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Director of Chemistry (Small Molecule Process Development and Manufacturing)

188 000 - 259 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Director of Chemistry (Small Molecule Process Development and Manufacturing) (Biotech/Pharmaceutical Process Chemistry): Leading scientific and engineering teams in the design, optimization, characterization, and manufacturing transfer of robust small-molecule processes for preclinical and clinical medicines with an accent on process understanding, safety, productivity, and CMC support. Focus on scaling chemical and biochemical processes, developing impurity controls and phase-appropriate knowledge packages, and guiding cross-functional teams toward regulatory filings and clinical supply.

Location: Cambridge, Massachusetts, United States

Base compensation: $188,000–$259,000 per year

Company

hirify.global is a biotechnology company developing life-changing medicines across multiple drug modalities.

What you will do

  • Lead scientific, engineering, development, and manufacturing teams through early- to late-phase small-molecule drug development.
  • Design and guide experiments to optimize and characterize chemical processes, improving process understanding, robustness, productivity, safety, and cost effectiveness.
  • Develop fundamental process knowledge for transferring chemical and biochemical processes from laboratory scale to manufacturing partners.
  • Collaborate with Process Engineering, Analytical Chemistry, Oligo Synthesis, Solid Form, and Separations functions to establish process controls and support clinical material supply.
  • Manage and mentor scientific colleagues while developing future scientific and engineering leaders.
  • Communicate research results, contribute to CMC activities and IND sections, engage with contract research organizations, and represent the organization at conferences and consortia.

Requirements

  • M.S. or Ph.D. with 12+ years of relevant pharmaceutical or biotechnology experience, including people management.
  • Strong expertise in pharmaceutical process chemistry and engineering, including synthetic strategies, impurity controls, analytical methods, purification, isolation, process characterization, process safety, and technology transfer.
  • Experience leading project teams delivering active pharmaceutical ingredients across multiple modalities.
  • Ability to lead teams ethically, collaboratively, effectively, and cross-functionally.
  • Excellent communication, interpersonal, problem-solving, and scientific leadership skills.

Nice to have

  • Experience working with external partners and representing an organization in external-facing settings.
  • Familiarity with regulatory requirements and CMC activities related to drug development.

Culture & Benefits

  • Collaborative environment grounded in scientific rigor, data-driven decision-making, inclusion, integrity, and accountability.
  • Medical, dental, vision, life, short-term disability, and long-term disability insurance.
  • Paid vacation, company holidays, end-of-year shutdown time, sick time, and paid parental leave.
  • 401(k) program with company matching, employee stock purchase plan, and short- and long-term incentive opportunities.
  • Fitness and wellness programs, tuition reimbursement of up to $10,000 per year, and employee resource groups.

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