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6 дней назад

Engineer II, CMC Development Operations (mRNA)

74 000 - 118 400$
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
Engineer II, CMC Development Operations (mRNA): Transferring and scaling DNA/RNA/LNP/DP processes from bench to pilot scale to generate material for developmental and toxicology studies, with an accent on technology transfer, process optimization, and batch execution. Focus on troubleshooting process deviations, improving process robustness, analyzing batch data, and leading technical workstreams in an onsite operations environment.

Location: Onsite at hirify.global’s Technology Center campus in Norwood, Massachusetts, United States; full-time onsite attendance is required and remote work is not eligible.

Salary: $74,000–$118,400 per year, with potential eligibility for an annual discretionary bonus, incentive compensation, or equity award.

Company

hirify.global develops mRNA medicines and operates a technology platform focused on reimagining how medicines are created and delivered.

What you will do

  • Transfer DNA/RNA/LNP/DP processes from bench to pilot scale and generate material for developmental and toxicology studies.
  • Lead or contribute to technology transfer, process optimization, continuous improvement, and process robustness projects.
  • Serve as batch lead, execute operations, troubleshoot issues in real time, and resolve process deviations.
  • Collaborate with Process Development, Analytical, and other cross-functional teams.
  • Analyze and communicate batch data to support process improvements and decision-making.
  • Author and optimize SOPs and protocols, support training, guide junior team members, and mitigate safety, process, and operational risks.

Requirements

  • Bachelor’s or Master’s degree in Life Sciences, Chemistry, Engineering, Pharmaceutical Sciences, Data Science, or a related technical discipline.
  • At least 2 years of relevant experience with a Bachelor’s degree or minimal experience with a Master’s degree; preferred experience is 2–3 years with a Master’s or 3–5 years with a Bachelor’s.
  • Hands-on process development or operations experience involving enzymatic reactions, chromatography, tangential flow filtration, or biologics formulation.
  • Experience with mRNA/DNA synthesis, LNP formulation, drug product processes, technology transfer, or process scale-up.
  • Ability to independently execute and troubleshoot processes, analyze complex datasets, and translate findings into improvements.
  • Full-time onsite work in Norwood, Massachusetts is required; the role is not eligible for remote work.

Culture & Benefits

  • Healthcare coverage and voluntary benefit programs.
  • Fitness, mindfulness, and mental health resources.
  • Family planning benefits, including fertility, adoption, and surrogacy support.
  • Paid time off, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown.
  • Savings and investment programs, plus location-specific perks.
  • In-person collaboration supported by a 70/30 work model.

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