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10 дней назад

Engineer II, Drug Product Development

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, Drug Product Development (Pharmaceutical Sciences/Biotechnology): Developing sterile drug product processes and products for clinical and future commercial supply with an accent on formulation, aseptic fill/finish operations, scale-up, and container compatibility. Focus on designing experiments, characterizing processing and stability, supporting technology transfer, and solving manufacturing process challenges.

Location: Norwood, Massachusetts, United States; full-time, on-site role with up to 20% travel.

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

Company

hirify.global develops mRNA technology and medicines for clinical and commercial use.

What you will do

  • Develop sterile drug product processes, formulations, and aseptic fill/finish unit operations for clinical and future commercial supply.
  • Conduct scale-up and technology-transfer studies covering freeze/thaw, mixing, filling, filtration, lyophilization, transport, and stability.
  • Develop protocols to evaluate compatibility with processing materials, container-closure components, and sterilization processes.
  • Plan and execute experiments using design of experiments where appropriate, then prepare protocols, presentations, and study reports.
  • Perform characterization activities including opacity testing, microscopy, and particle sizing, while supporting troubleshooting and investigations.
  • Collaborate with analytical development, pilot operations, manufacturing, and other interdisciplinary groups to solve formulation and process challenges.

Requirements

  • Master’s or bachelor’s degree in chemical engineering, biochemical or biomedical engineering, pharmaceutical sciences, materials science, or a related discipline.
  • 0–2 years of relevant experience after a master’s degree or at least 2 years after a bachelor’s degree.
  • Strong laboratory skills and the ability to work efficiently in a dynamic environment.
  • Knowledge of statistical design of experiments and data analysis.
  • Ability to work on-site in Norwood, Massachusetts, United States.
  • Access to export-controlled information may require U.S. person status or an export license.

Nice to have

  • Experience in the biopharma, biopharmaceutical, pharmaceutical, or biotechnology industry.
  • Knowledge of GMP compliance.
  • Knowledge of nucleic acid chemistry and biology.

Culture & Benefits

  • Healthcare coverage and voluntary benefits.
  • Fitness, mindfulness, and mental health resources.
  • Family planning support, including fertility, adoption, and surrogacy benefits.
  • Paid vacation, volunteer days, sabbatical, global recharge days, and discretionary year-end shutdown.
  • Savings and investment programs, plus location-specific benefits.

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