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7 дней назад

Manufacturing Associate I, Drug Substance Operations (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, Drug Substance Operations (mRNA): Producing mRNA drug substance through controlled GMP manufacturing operations with an accent on aseptic processing, cleanroom execution, documentation, and data integrity. Focus on operating manufacturing equipment and digital systems, maintaining compliant production areas, and executing technical processes accurately and consistently.

Location: Norwood, Massachusetts, United States; onsite manufacturing role. Only U.S. persons are eligible due to U.S. export control requirements.

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

Company

hirify.global develops mRNA technology, vaccines, and therapeutics for infectious diseases, immuno-oncology, rare diseases, and cardiovascular diseases.

What you will do

  • Execute 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 real-time documentation according to good documentation practices and data integrity standards.
  • 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 controls.
  • Collaborate with cross-functional partners, escalate issues early, and support consistent execution across operations.

Requirements

  • Bachelor’s degree in a STEM field with 0–1 years of relevant experience, an associate’s degree with 2–4 years of relevant experience, or a high school diploma with more than 4 years of relevant experience.
  • Strong attention to detail, disciplined execution, accountability, and the ability to learn technical processes.
  • Comfort working in a cleanroom and following defined procedures in a structured environment.
  • Experience or interest in manufacturing, operations, biopharma, life sciences, or other regulated technical environments.
  • Must qualify as a U.S. person under U.S. export control laws; non-U.S. persons are not eligible for this position.

Culture & Benefits

  • Healthcare 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 discretionary year-end shutdown.
  • Savings and investment programs plus location-specific benefits.

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