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9 дней назад

gRNA Process Development Scientist (CRISPR)

32 - 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
gRNA Process Development Scientist (CRISPR): Developing manufacturing processes and controls for gRNA drug substances by synthesizing, purifying, and characterizing oligonucleotides with an accent on solid-phase synthesis, chromatography, and analytical testing. Focus on scaling and transferring oligonucleotide manufacturing processes, operating HPLC and TFF systems, and maintaining reliable laboratory documentation and safety.

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

Salary: USD 32.00-41.00 per hour

Company

hirify.global is an international life sciences company providing analytical testing, laboratory, genomics, pharmaceutical, and agroscience services.

What you will do

  • Develop gRNA drug substance manufacturing processes and controls for clinical-stage programs.
  • Execute solid-phase synthesis, purification, scale-up, and process transfer experiments for oligonucleotide drug substances.
  • Perform routine analytics using HPLC, UV-Vis, chromatography systems, gel electrophoresis, and NanoDrop.
  • Prepare buffers, reagents, and stock solutions according to established recipes and SOPs.
  • Compile and present experimental data to team members and stakeholders.
  • Maintain laboratory records and equipment, order materials, support troubleshooting, and uphold laboratory safety standards.

Requirements

  • B.S. or M.S. degree in chemistry, chemical engineering, biochemistry, or a related field, plus at least two years of relevant laboratory industry experience.
  • Experience with oligonucleotide synthesis and purification equipment.
  • Experience with Tangential Flow Filtration (TFF) is required.
  • Experience with Akta chromatography systems, Agilent U/HPLC, gel electrophoresis, and NanoDrop.
  • Experience with good documentation practices and electronic laboratory notebooks such as Benchling.
  • Authorization to work in the United States indefinitely without restriction or sponsorship is preferred.

Nice to have

  • Background in CRISPR gRNA development.
  • Experience with gRNA or longmer synthesis and purification development.

Culture & Benefits

  • Professional growth opportunities and support for entering and advancing in the biopharmaceutical industry.
  • Work-life balance and a supportive team environment.
  • Medical, dental, and vision coverage.
  • Life and disability insurance.
  • 401(k) with company match, paid vacation, and paid holidays.
  • Eligibility for yearly goal-based bonuses and merit-based increases.

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