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8 дней назад

Manufacturing Process Technician - Bulk Drug Substance Manufacturing Services - Night Shift (Biotechnology)

54 411 - 73 614$
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

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TL;DR
Manufacturing Process Technician - Bulk Drug Substance Manufacturing Services - Night Shift (Biotechnology): Operating and monitoring floor-based processes for cGMP drug substance manufacturing at Amgen’s advanced FleX Batch facility with an accent on aseptic techniques, equipment operation, buffer and media preparation, and strict documentation. Focus on performing hands-on production activities, maintaining compliance with GMP procedures, and supporting reliable 24/7 manufacturing on a 12-hour night-shift schedule.

Location: Holly Springs, North Carolina, United States; onsite night shift. The role supports 24/7 manufacturing on a 12-hour 2-2-3 schedule from 5:45 p.m. to 6:15 a.m., including some holidays, inclement weather, and requested overtime.

Salary: USD 54,411.05–73,614.95 per year, plus benefits and total rewards.

Company

hirify.global is a biotechnology company developing treatments and operating an advanced drug substance manufacturing facility with disposable technologies, stainless-steel equipment, industry 4.0 capabilities, and sustainability initiatives.

What you will do

  • Perform hands-on setup, cleaning, sanitization, and monitoring of manufacturing equipment.
  • Prepare and transfer buffers and media.
  • Weigh and dispense materials used in buffer and media preparation.
  • Complete washroom activities and clean production equipment from small to large scale.
  • Run and monitor critical processes according to assigned procedures.
  • Complete equipment logs, electronic batch records, and other required documentation while maintaining a clean, organized workspace.

Requirements

  • High school diploma or GED plus at least one year of manufacturing or other regulated-industry experience, or an associate’s degree.
  • Follow cGMP procedures, SOPs, manufacturing procedures, job hazard analyses, and applicable regulations.
  • Apply proper gowning and aseptic techniques.
  • Demonstrate strong verbal and written communication and close attention to detail.
  • Work the assigned 12-hour night shift and maintain regular attendance to support 24/7 operations.
  • Use Microsoft Office and electronic systems such as EBR/MES, Delta V, and electronic quality systems.

Nice to have

  • NC BioWorks Certificate Program completion.
  • Experience in biotechnology, pharmaceuticals, or another regulated industry.
  • Basic understanding of GMP principles.

Culture & Benefits

  • Competitive base salary aligned with local industry standards.
  • Comprehensive total rewards and benefits plans.
  • Collaborative and inclusive environment focused on advancing science and serving patients.
  • Support for professional growth and personal well-being.

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