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7 дней назад

Manufacturing Associate I (mRNA Manufacturing)

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 Manufacturing): Producing mRNA drug substance in a GMP-regulated cleanroom environment with an accent on aseptic processing, formulation, filtration, mixing, filling, dispensing, and real-time documentation. Focus on executing controlled manufacturing procedures, operating digital manufacturing systems, maintaining data integrity, and identifying and escalating issues during site-based production.

Location: 100% onsite in Norwood, Massachusetts, United States; only U.S. persons are eligible due to export control requirements.

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

Company

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

What you will do

  • Execute manufacturing operations using approved procedures, batch records, and work instructions in a GMP-regulated environment.
  • Perform cleanroom operations and support aseptic processing, formulation, filtration, mixing, filling, and dispensing of mRNA drug substance.
  • Complete real-time documentation according to good documentation practices and data integrity standards.
  • Operate 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 teammates and cross-functional partners, communicate clearly, escalate issues early, and maintain required training and gowning qualifications.

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.
  • Ability to learn technical processes, follow defined procedures, maintain accuracy, and work consistently in a structured environment.
  • Comfort working in a cleanroom and following gowning, safety, documentation, and compliance requirements.
  • Must qualify as a U.S. person under U.S. export control laws; non-U.S. persons are not eligible for this position.

Nice to have

  • Strong attention to detail, sound judgment, professionalism, and accountability.
  • Team-first mindset and willingness to support shared manufacturing goals.
  • Continuous-improvement mindset and confidence to speak up and escalate issues appropriately.

Culture & Benefits

  • 100% onsite work model with direct collaboration, mentorship, and hands-on operational support.
  • Healthcare and voluntary benefit programs.
  • Fitness, mindfulness, and mental-health resources.
  • Family-planning support, including fertility, adoption, and surrogacy benefits.
  • Paid vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown.
  • Retirement savings and location-specific benefits.

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