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6 дней назад

Manufacturing Process Technician (Biotech)

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 (Biotech): Performing bulk manufacturing processes in aseptic and non-aseptic environments with an accent on equipment operation, materials handling, batch documentation, and GMP compliance. Focus on cleaning and operating processing equipment, preparing and transferring solutions, collecting samples, and accurately completing electronic batch records during rotating 12-hour shifts.

Location: West Greenwich, Rhode Island, United States; onsite 12-hour rotating shift

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, and set up and break down single-use materials.
  • Weigh and dispense raw materials, prepare and transfer solutions, and handle manufacturing materials.
  • Operate and monitor clean systems, autoclaves, processing equipment, and powered industrial vehicles.
  • Collect, process, store, and deliver samples, and reconcile products and components.
  • Complete process documentation accurately and follow current good manufacturing practices.

Requirements

  • High school diploma or GED plus one year of manufacturing, operations, or military experience, or an associate's degree.
  • Ability to work a rotating 12-hour shift from 7 a.m. to 7 p.m., covering seven days per week on a two-week rotation.
  • Ability to stand or sit for extended periods, maintain focus during repetitive tasks, and perform physical manufacturing duties.
  • Ability to assemble, disassemble, operate, and understand simple to moderately complex equipment according to procedures.
  • Ability to follow written procedures, recognize and report malfunctions, communicate effectively, and work independently and in a team.
  • Onboarding schedule: administrative Monday–Friday hours, approximately 8 a.m. to 5 p.m., for 2–6 weeks.

Nice to have

  • Experience in a GMP or other regulated environment.
  • Knowledge of GMP principles or drug substance manufacturing.
  • Experience documenting process tasks in electronic batch records.
  • Understanding of measurements, calculations, and the metric system.
  • Strong attention to detail and demonstrated ability to accept coaching and improve.

Culture & Benefits

  • Health, dental, vision, life, disability, and flexible spending benefits.
  • Retirement and savings plan with company contributions.
  • Annual bonus program and stock-based long-term incentives.
  • Paid time-off plans and career development opportunities.
  • Additional 15% shift differential for the rotating shift, with an average of 14 shift days per month and every other weekend off.

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