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4 дня назад

Associate II, Quality Control (Pharmaceutical Manufacturing)

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
Associate II, Quality Control (Pharmaceutical Manufacturing): Performing cGMP in-process, release, and stability testing for pharmaceutical materials and products with an accent on analytical chemistry, regulatory compliance, and data integrity. Focus on operating HPLC and other laboratory equipment, investigating OOS/OOT/deviations, maintaining controlled documentation, and supporting CAPAs and laboratory operations.

Location: 100% onsite in Norwood, Massachusetts, United States

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

Company

hirify.global develops mRNA technology and medicines through a biotechnology platform.

What you will do

  • Perform cGMP in-process, release, and stability testing for raw materials, drug substances, intermediates, and drug products.
  • Operate analytical equipment including HPLC, UPLC, UV plate readers, particulate matter and particle-size analysis systems, KF, and osmolality instruments.
  • Document procedures and results in assay worksheets and LIMS in accordance with GDP and data-integrity requirements.
  • Support laboratory operations, including reagent preparation, sample management, equipment maintenance, inventory control, housekeeping, and 5S activities.
  • Assist with assay and equipment troubleshooting, laboratory investigations, OOS/OOT/OOE investigations, deviations, CAPAs, and effectiveness checks.
  • Review, write, and revise SOPs, protocols, and reports while supporting special projects and maintaining a safe laboratory environment.

Requirements

  • BA or BS in Chemistry preferred, or another relevant scientific discipline.
  • At least two years of quality control laboratory experience in a pharmaceutical company.
  • Knowledge of cGMP, SOP, FDA, ICH, GDP, and data-integrity requirements.
  • Must work onsite in Norwood, Massachusetts.
  • Only U.S. persons—citizens, permanent residents, asylees, or refugees—are eligible due to U.S. export-control requirements.
  • Visa sponsorship for non-U.S. persons is not available.

Culture & Benefits

  • In-person work model with direct collaboration, mentorship, and hands-on laboratory support.
  • Healthcare 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 discretionary year-end shutdown.
  • Savings and investment programs, plus location-specific benefits.

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