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6 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): Producing mRNA drug substance in a GMP-regulated cleanroom environment with an accent on aseptic processing, formulation, filtration, mixing, filling, and real-time documentation. Focus on executing controlled manufacturing procedures, operating digital systems and equipment, maintaining data integrity, and recognizing and escalating process issues.

Location: 100% onsite in Norwood, Massachusetts, United States. Applicants must qualify as U.S. persons under U.S. export control requirements.

Salary: $53,500–$85,600 per year, with potential annual bonus, incentive compensation, or equity.

Company

A biotechnology company developing mRNA-based medicines and vaccines through an integrated technology, manufacturing, and research platform.

What you will do

  • Execute mRNA drug substance manufacturing operations using approved procedures, batch records, and work instructions in a GMP-regulated environment.
  • Perform cleanroom and aseptic processing activities, including formulation, filtration, mixing, filling, and dispensing.
  • Complete manufacturing documentation in real time while maintaining data integrity and good documentation practices.
  • Operate and learn manufacturing systems and equipment, including SAP, Veeva, DeltaV, Syncade, LIMS, and CMMS.
  • Maintain production-area cleanliness, readiness, safety, waste handling, and environmental compliance.
  • Collaborate with manufacturing and cross-functional partners, communicate clearly, and escalate issues early.

Requirements

  • Bachelor’s degree in a STEM field with 0–1 years of relevant industry experience, or an Associate’s degree with 2–4 years of relevant experience, or a high school diploma with more than 4 years of relevant experience.
  • Experience in manufacturing, operations, biopharma, life sciences, or another regulated or technical environment is helpful.
  • Strong attention to detail, disciplined execution, accountability, and the ability to learn and reliably apply technical processes.
  • Comfort working in a cleanroom and following defined procedures, gowning requirements, and assigned-operation qualifications.
  • Must qualify as a U.S. person under U.S. export control laws; non-U.S. persons cannot be sponsored for an export control license.
  • Must work onsite in Norwood, Massachusetts.

Culture & Benefits

  • In-person, site-based work with direct mentorship, real-time collaboration, and hands-on operational support.
  • Competitive healthcare and voluntary benefit programs.
  • Fitness, mindfulness, mental-health, family-planning, 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.

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