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5 дней назад

Manufacturing Associate I (mRNA)

53 500 - 85 600$
Формат работы
onsite
Тип работы
fulltime
Грейд
junior
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
Manufacturing Associate I (mRNA): Executing GMP manufacturing operations for mRNA and LMX/LNP drug substances in a clean-room environment with an accent on aseptic processing, chromatography, filtration, nano-mixing, and filling. Focus on following batch records and SOPs precisely, maintaining data integrity and area control, and performing trained unit operations for clinical and commercial products.

Location: Norwood, Massachusetts, United States; 100% onsite. Due to U.S. export control requirements, only U.S. persons—citizens, permanent residents, asylees, or refugees—are eligible. hirify.global cannot sponsor non-U.S. persons for an export control license.

Salary: $53,500–$85,600 per year, plus potential discretionary bonus, incentive compensation, or equity subject to eligibility.

Company

hirify.global develops mRNA medicines and operates a technology platform for transforming how medicines are created and delivered.

What you will do

  • Execute manufacturing unit operations for mRNA and LMX/LNP drug substances under close supervision in a GMP-regulated clean-room environment.
  • Perform aseptic processing using chromatography, filtration methods, and nano-mixing technologies for clinical and commercial products.
  • Complete filling and dispensing activities through final container closure before forward processing.
  • Follow SOPs, work instructions, batch records, GMP regulations, safety procedures, and Good Documentation Practices.
  • Maintain Grade C manufacturing areas, handle waste according to documented procedures, and support environmental compliance.
  • Use manufacturing systems and equipment such as SAP, Veeva, DeltaV, Syncade, LIMS, and CMMS, including basic troubleshooting after training.

Requirements

  • High school diploma required.
  • Qualifying experience includes a STEM degree with 0–1 years of industry experience, an associate degree with 2–3 years of industry experience, or a high school diploma with 3–5 years of industry experience.
  • Ability to learn and develop a strong understanding of GMP regulations.
  • Ability to work onsite in Norwood, Massachusetts, with periods of standing and lifting in a clean-room environment.
  • Must qualify as a U.S. person under applicable export control requirements.

Culture & Benefits

  • In-person work model with direct collaboration, mentorship, and hands-on site-based operations.
  • Healthcare and voluntary benefit programs.
  • Fitness, mindfulness, and mental health resources.
  • Family planning benefits, including fertility, adoption, and surrogacy support.
  • Paid time off including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown.
  • Savings and investment programs plus location-specific perks.

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