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3 дня назад

Scientist I, mRNA, Process Development (Biotech)

105 000 - 145 000$
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
Scientist I, mRNA, Process Development (Biotech): Developing, optimizing, and scaling mRNA synthesis, purification, and characterization processes with an accent on in-vitro transcription, plasmid DNA linearization, chromatography, and tangential flow filtration. Focus on transferring mRNA drug-substance processes from bench scale to GMP manufacturing, supporting mRNA therapeutics projects, and ensuring product quality through analytical characterization.

Location: Waltham, Massachusetts, United States

Salary: $105,000–$145,000 per year

Company

hirify.global is a technology-driven biotechnology company providing integrated technologies, services, and manufacturing expertise for advanced therapies from design through commercialization.

What you will do

  • Lead development, optimization, and scale-up experiments for mRNA production and purification.
  • Characterize mRNA samples using electrophoresis, spectrophotometry, HPLC, and UPLC.
  • Support tech transfer of mRNA-based therapeutics from process development into manufacturing.
  • Collaborate with MSAT, analytical development, external clients, and business development teams.
  • Prepare statements of work and proposals, communicate experimental results, and develop SOPs and technical documents.

Requirements

  • BS or MS in Microbiology, Bioengineering, Biochemistry, or a related discipline, plus 8+ years of relevant experience.
  • At least 4 years of experience working with mRNA-based therapeutics.
  • Hands-on experience with in-vitro transcription, plasmid DNA linearization, mRNA downstream processing, TFF, and chromatography.
  • Experience operating ÄKTA Avant/Pure systems and Repligen KrosFlow Kr2i filtration skids.
  • Experience with mRNA process technology transfer and scaling from bench scale to GMP manufacturing.

Nice to have

  • Experience with mRNA-LNP formulation and mixing technologies.
  • Experience using JMP for Design of Experiments and data analysis.
  • Familiarity with GMP regulations, Quality by Design principles, and regulatory filing documentation.

Culture & Benefits

  • Regular employment within the Process Development department.
  • Work with cross-functional teams and external clients on advanced mRNA therapeutics.
  • Equal employment opportunity and reasonable accommodations for qualified applicants with disabilities.

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