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3 дня назад

Research Scientist III (Biopharmaceutical Development)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Релокация
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
Research Scientist III (Biopharmaceutical Development): Leading experiments for process development, optimization, characterization, and analytical method development in a GMP environment with an accent on solid oral dosage, biologics, and advanced characterization techniques. Focus on designing statistically robust studies, troubleshooting complex technical issues, preparing regulatory documentation, and guiding junior scientists.

Location: Tampa, Florida, United States; fully site-based. Relocation assistance is available for eligible candidates and their families.

Company

hirify.global is a global life sciences company with more than 30 sites across five continents, developing and manufacturing medicines and supporting customers in turning breakthrough ideas into therapies.

What you will do

  • Lead the design, execution, and interpretation of experiments for process development, optimization, and characterization in a GMP environment.
  • Develop and implement analytical methods for drug substance, drug product, and biopharmaceutical development.
  • Troubleshoot complex technical issues and propose timely, effective solutions.
  • Author and review technical reports, protocols, and regulatory documents, and present findings to internal and external stakeholders.
  • Collaborate with process development, manufacturing, quality control, and regulatory affairs teams.
  • Mentor junior scientists and ensure compliance with safety regulations and company policies.

Requirements

  • Ph.D. in Biochemistry, Molecular Biology, Chemical Engineering, or a related discipline with 5+ years of relevant industry experience; alternatively, an M.S. with 8+ years or a B.S. with 10+ years of experience.
  • 5–10 years of solid oral dosage development experience; DPI experience is preferred.
  • Hands-on experience in mammalian cell culture, upstream or downstream process development, or analytical method development for biologics.
  • Expertise in experimental design, statistical data analysis, cGMP regulations, and biopharmaceutical regulatory requirements.
  • Experience with HPLC, mass spectrometry, CE, SPR, or other advanced analytical techniques.
  • Strong scientific communication, project leadership, problem-solving, and scientific reporting skills.

Nice to have

  • DPI (Drug Products Inhalation) development experience.
  • Knowledge of ICH and ICH Q8 practices.

Culture & Benefits

  • Agile career environment and dynamic working culture.
  • Inclusive and ethical workplace focused on collaboration, accountability, excellence, passion, and integrity.
  • Performance-oriented compensation programs.
  • Benefits vary by role and location.
  • In-person collaboration supports technical precision and the manufacture of medicines to high quality and safety standards.

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