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6 дней назад

Manufacturing Process Technician - Nights (Biotech Manufacturing)

Формат работы
onsite
Тип работы
fulltime
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 Process Technician - Nights (Biotech Manufacturing): Performing bulk drug-substance manufacturing processes in aseptic and non-aseptic environments with an accent on GMP compliance, equipment operation, materials handling, and electronic batch-record documentation. Focus on operating clean systems and autoclaves, managing cryogenic systems, completing process calculations, and maintaining accurate manufacturing records during the night shift.

Location: West Greenwich, Rhode Island, United States; onsite night-shift role

Company

hirify.global is a biotechnology company researching, manufacturing, and delivering medicines for serious illnesses across oncology, inflammation, general medicine, and rare disease.

What you will do

  • Perform simple to moderately complex bulk-manufacturing processes according to standard operating procedures and batch records.
  • Clean equipment and parts using manual and automated methods in aseptic and non-aseptic environments.
  • Set up and break down single-use materials, weigh and dispense raw materials, and handle manufacturing materials.
  • Operate and monitor clean systems, autoclaves, processing equipment, cryogenic systems, and power industrial vehicles.
  • Collect, process, store, and deliver samples; reconcile products and components.
  • Complete process documentation, calculations, CIP and SIP operations, and other assigned manufacturing tasks in accordance with current GMP requirements.

Requirements

  • High school diploma or GED plus at least one year of manufacturing or operations experience, or military experience; alternatively, an associate's degree.
  • Ability to follow written procedures, recognize and report malfunctions, and accurately complete electronic batch records.
  • Ability to operate, assemble, and disassemble simple to moderately complex equipment.
  • Basic understanding of measurements, calculations, and the metric system.
  • Ability to stand or sit for extended periods, maintain focus during repetitive tasks, and work with strong attention to detail.
  • Ability to work independently and in a team, communicate effectively, and respond constructively to coaching.

Nice to have

  • At least one year of experience in a GMP or other regulated environment.
  • Knowledge of GMP principles and drug-substance manufacturing experience.

Culture & Benefits

  • Health, dental, and vision coverage, life and disability insurance, and flexible spending accounts.
  • Retirement and savings plan with company contributions.
  • Discretionary annual bonus program and stock-based long-term incentives.
  • Paid time-off plans and career development opportunities.
  • Collaborative, innovative, science-based work environment focused on serving patients.

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