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2 дня назад

Late-Stage LNP Process Development Scientist

36 - 41$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
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
Late-Stage LNP Process Development Scientist (LNP drug product manufacturing): Supporting process development, scale-up, and characterization of clinical-stage lipid nanoparticle drug products with an accent on mixing, tangential flow filtration, and in-process analytics. Focus on designing and executing laboratory experiments, analyzing process data, improving process understanding, and documenting science-based manufacturing solutions.

Location: Boston, MA, USA; candidates must live within a commutable distance. Full-time, Monday–Friday, 8:00am–5:00pm, with overtime as needed.

Salary: USD 36.00–41.00 per hour

Company

hirify.global is an international life sciences company providing analytical testing, laboratory, pharmaceutical, genomics, discovery pharmacology, CDMO, and clinical study support services.

What you will do

  • Support process development, scale-up, and process characterization for LNP clinical-stage drug products across 10 mg to 1 gram batch ranges.
  • Execute in-process analytics, including dynamic light scattering, UV quantification via Ribogreen, pH, and osmolality.
  • Perform laboratory experiments with limited supervision under subject matter expert guidance.
  • Organize, analyze, interpret, and present data to process development and cross-functional teams.
  • Author SOPs, technical reports, and protocols, and document experiments in electronic lab notebooks such as Benchling.
  • Maintain laboratory equipment, order critical reagents, and support operational excellence activities.

Requirements

  • B.S. in chemical or biomedical engineering, chemistry, biological sciences, or a related field with 3–4 years of relevant laboratory experience; or an M.S. in biological or biochemical sciences with 1–2 years of relevant experience.
  • Experience with bench-scale LNP drug product manufacturing, especially mixing and tangential flow filtration processes.
  • Experience with nucleic acid process development, dynamic light scattering, and osmolality monitoring.
  • Experience using electronic lab notebooks such as Benchling and preparing SOPs, technical reports, and protocols.
  • Strong data analysis, troubleshooting, problem-solving, communication, organization, and time-management skills.
  • Authorization to work indefinitely in the United States without restriction or sponsorship is required.

Nice to have

  • Experience with UV quantification via Ribogreen.
  • Experience with GMP manufacturing practices, tech transfer, T-mixing and TFF.
  • Experience with statistical analysis software such as JMP or Design-Expert.

Culture & Benefits

  • Collaborative, cross-functional environment focused on science-based manufacturing solutions for complex nucleic acid drug products.
  • Professional growth opportunities within the biopharmaceutical industry.
  • Medical, dental, and vision coverage, plus life and disability insurance.
  • 401(k) with company match, paid vacation and holidays.
  • Yearly goal-based bonus eligibility and merit-based increases.

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