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8 дней назад

Manufacturing Associate II (mRNA)

63 200 - 100 900$
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
Manufacturing Associate II (mRNA) (cGMP aseptic manufacturing): Performing formulation, sterile filtration, vial and syringe filling, visual inspection, and compliant batch documentation in an onsite drug-product manufacturing operation with an accent on aseptic processing, equipment readiness, and right-first-time execution. Focus on maintaining controlled manufacturing conditions, investigating deviations, supporting continuous improvement, and coordinating with QA, QC, MS&T, Facilities, and Supply Chain.

Location: 100% onsite in Norwood, Massachusetts, United States; 12-hour night shift from 6:00 PM to 6:00 AM, with flexibility for overtime, weekends, holidays, and operational coverage. Only U.S. persons are eligible due to U.S. export control requirements.

Salary: $63,200–$100,900 per year, plus potential annual bonus, incentive compensation, or equity subject to eligibility.

Company

hirify.global develops mRNA-based medicines, vaccines, delivery technologies, and manufacturing capabilities for infectious diseases, oncology, rare diseases, and cardiovascular diseases.

What you will do

  • Perform formulation, sterile filtration, vial and syringe filling, aseptic line clearances, and downstream visual inspection in accordance with SOPs and cGMP requirements.
  • Prepare materials and components, check equipment, maintain cleanrooms, and keep facilities and equipment within defined operating parameters.
  • Complete contemporaneous ALCOA+ documentation in logbooks, MES, and electronic batch records.
  • Perform in-process checks, identify and escalate deviations or equipment issues, and support troubleshooting and investigations.
  • Support SOP and work-instruction updates, continuous improvement, cross-training, and peer mentoring.
  • Collaborate with QA, QC, MS&T, Facilities, Supply Chain, and other partners during manufacturing operations and issue resolution.

Requirements

  • Associate or bachelor's degree in a scientific field, or a high school diploma with equivalent experience.
  • 2–4 years of GMP manufacturing or a similar experience preferred; strong entry-level candidates may be trained.
  • Comfort working in cleanrooms with full gowning, standing for extended periods, and lifting approximately 35 pounds.
  • Basic computer skills for batch records and training systems, plus reliable, detail-oriented communication and teamwork.
  • 20/20 corrected vision and the ability to see all colors across the visible spectrum; vision testing is required at hiring and annually thereafter.
  • Must be eligible as a U.S. person under U.S. export control requirements; visa sponsorship for non-U.S. persons is unavailable.

Culture & Benefits

  • Fully onsite, in-person manufacturing environment with direct collaboration, mentorship, and hands-on operational support.
  • Healthcare coverage and voluntary benefit programs.
  • Fitness, mindfulness, and mental health resources.
  • Family planning benefits, including fertility, adoption, and surrogacy support.
  • Paid vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown.
  • Savings and investment programs, plus location-specific benefits.

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