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2 дня назад

Process Development Senior Scientist (Synthetic Peptides)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
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
Process Development Senior Scientist (Synthetic Peptides): Developing scalable solid-phase peptide synthesis processes for therapeutic peptides from pre-IND through commercial production with an accent on purification, characterization, GMP manufacturing, and technology transfer. Focus on advancing synthesis technologies, modeling and characterizing process performance, supporting regulatory filings, and solving complex process-development challenges across interdisciplinary teams.

Location: Thousand Oaks, California or Cambridge, Massachusetts campus, United States

Company

hirify.global is a biotechnology company researching, manufacturing, and delivering medicines for serious illnesses across oncology, inflammation, general medicine, and rare disease.

What you will do

  • Develop scalable synthetic processes for therapeutic peptides using solid-phase peptide synthesis.
  • Advance innovation in solid-phase synthesis, purification, characterization, sustainability, and process efficiency.
  • Support cGMP manufacturing and technology transfer to external contract manufacturers.
  • Ensure process performance through process understanding, modeling, and characterization.
  • Provide experimental results, technical updates, documentation, data interpretation, and recommendations to drug substance development teams.
  • Prepare regulatory documentation, support filings, and serve as a technical expert in solid-phase peptide synthesis.

Requirements

  • PhD, PharmD, or MD with relevant postdoctoral experience; or a master’s degree with 3 years of scientific experience; or a bachelor’s degree with 5 years of scientific experience.
  • Expertise in synthetic peptide process development, including hands-on synthesis and purification of peptides produced by solid-phase synthesis.
  • Experience developing, scaling, and transferring solid-phase peptide synthesis processes into GMP manufacturing within the pharmaceutical or biotechnology industry.
  • Proficiency with analytical characterization techniques including HIC-HPLC, SEC, LC-MS, IEX, and RP-HPLC.
  • Ability to work independently and collaboratively in interdisciplinary teams while planning and delivering complex projects.
  • Excellent written and verbal communication skills.

Nice to have

  • PhD in organic chemistry, biochemistry, or chemical engineering.
  • Familiarity with laboratory automation, data analysis, and data visualization tools.
  • Peer-reviewed publications and research presentations.
  • Research summary included with the CV.

Culture & Benefits

  • Collaborative, innovative, and science-based work environment.
  • Health, dental, vision, life, disability, and flexible spending benefits.
  • Retirement and savings plan with company contributions.
  • Annual bonus program and stock-based long-term incentives.
  • Paid time off, work-life balance support, and career development opportunities.
  • Sponsorship for this role is not guaranteed.

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