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8 дней назад

Manufacturing Process Technician - Nights

54 411 - 73 615$
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 Process Technician - Nights (Biotech Manufacturing): Performing bulk manufacturing processes in aseptic and non-aseptic environments with an accent on equipment operation, materials handling, sampling, cleaning, and cGMP documentation. Focus on operating clean systems, autoclaves, cryogenic systems, and processing equipment while maintaining accurate batch records and product reconciliation.

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

Salary: $54,411.05–$73,614.95 per year

Company

hirify.global is a biotechnology company developing and manufacturing 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, and set up or break down single-use materials.
  • Weigh and dispense raw materials, handle materials, and operate power industrial vehicles.
  • Operate and monitor clean systems, autoclaves, processing equipment, cryogenic systems, and CIP/SIP processes.
  • Collect, process, store, and deliver samples, and complete product and component reconciliation.
  • Complete process documentation accurately, perform calculations, and follow current GMP requirements.

Requirements

  • High school diploma/GED plus at least one year of manufacturing, operations, or military experience, or an associate degree.
  • Ability to follow written procedures, recognize and report malfunctions, and document tasks in electronic batch records.
  • Ability to assemble, disassemble, operate, and understand 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 perform work with close attention to detail.
  • Ability to communicate effectively and work independently and as part of a team.

Nice to have

  • At least one year of experience in a GMP or other regulated environment.
  • Knowledge of GMP principles and experience in drug substance manufacturing.
  • Ability to receive coaching and demonstrate measurable improvement.

Culture & Benefits

  • Collaborative, innovative, and science-based work environment.
  • Health, dental, vision, life, disability, and flexible spending benefits.
  • 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.
  • Sponsorship is not guaranteed; reasonable accommodations are available during hiring and employment.

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