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5 дней назад

Manufacturing Process Technician - Solution Prep (Nights) (Biotech)

54 411 - 73 614$
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 - Solution Prep (Nights) (Biotech): Performing bulk manufacturing and solution preparation in aseptic and non-aseptic environments with an accent on equipment cleaning, raw-material weighing, process monitoring, and cGMP documentation. Focus on operating manufacturing systems, handling materials and samples, completing electronic batch records, and maintaining accuracy across rotating 12-hour shifts.

Location: West Greenwich, Rhode Island, United States; onsite role. The position follows a rotating 12-hour shift schedule, with onboarding on a Monday–Friday administrative schedule for approximately 2–6 weeks.

Salary: $54,411.05–$73,614.95 per year, plus a 15% shift differential.

Company

hirify.global is a biotechnology company developing, 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 or 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 power industrial vehicles.
  • Collect, process, store, and deliver samples; reconcile products and components.
  • Complete process documentation accurately, perform calculations, and follow current cGMP requirements.

Requirements

  • High school diploma/GED plus one year of manufacturing, operations, or military experience, or an associate’s degree.
  • Ability to follow written procedures, recognize and report malfunctions, and complete repetitive physical tasks with sustained attention to detail.
  • Ability to assemble, disassemble, operate, and understand simple to moderately complex equipment.
  • Basic understanding of measurements, calculations, and the metric system.
  • Ability to work effectively independently and as part of a shift team, with strong communication skills.
  • Ability to work a rotating 12-hour schedule, including coverage across seven days per week.

Nice to have

  • Experience in a GMP or other regulated environment.
  • Knowledge of GMP principles or drug-substance manufacturing experience.
  • Experience documenting process tasks in electronic batch records.
  • Ability to accept coaching and demonstrate measurable improvement.

Culture & Benefits

  • Comprehensive medical, dental, vision, life, disability, and flexible spending benefits.
  • Retirement and savings plan with company contributions.
  • Annual bonus program, stock-based long-term incentives, and paid time-off plans.
  • Career development opportunities and support for professional and personal well-being.
  • Flexible work models where applicable to the role.

Hiring process

  • Applications are accepted until a sufficient number of candidates are received or a candidate is selected.
  • Sponsorship for this role is not guaranteed.

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