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5 дней назад

Associate Manufacturing - Solution Prep (Nights) (Biotech)

70 985 - 96 038$
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
Associate Manufacturing - Solution Prep (Nights) (Biotech): Performing solution manufacturing operations, including batching and transferring buffers and media, at a biotechnology facility with an accent on GMP compliance, batch-record documentation, and process monitoring. Focus on troubleshooting production equipment, maintaining manufacturing procedures, managing deviations, and implementing routine process improvements.

Location: West Greenwich, Rhode Island, United States; onsite manufacturing facility. The role works a rotating 12-hour night shift from 7:00 PM to 7:00 AM. Initial onboarding and training lasts 2–6 weeks on an administrative Monday–Friday schedule, approximately 8:00 AM–5:00 PM.

Annual salary: $70,985.20–$96,038.80 USD, plus a 15% night-shift differential and premium pay for Sundays worked.

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 batching and transfer of buffers and media according to standard operating procedures.
  • Monitor critical manufacturing processes and complete routine validation protocols.
  • Prepare, revise, and document manufacturing procedures, SOPs, batch records, and technical reports.
  • Conduct basic troubleshooting and review documentation for assigned functions.
  • Initiate and own area deviations, revise SOPs, and support LEAN activities.
  • Identify, recommend, and implement improvements to routine manufacturing functions.

Requirements

  • High school diploma or GED plus 2 years of manufacturing or operations experience; or an associate degree plus 6 months of relevant experience; or a bachelor’s degree in a related field.
  • Ability to understand, apply, and document Good Manufacturing Practices (GMP) in batch records.
  • Ability to work a rotating 12-hour night schedule and complete onsite manufacturing duties.
  • Preferred knowledge of biotechnology operations, including purification, cell culture, or aseptic processing.
  • Preferred knowledge of single-use systems, CFR and regulatory requirements, analytical methods, chemistry, biology, and physical principles.
  • Preferred troubleshooting, technical writing, project management, presentation, and laboratory equipment experience, including Delta V.

Culture & Benefits

  • Collaborative, innovative, science-based work environment focused on serving patients.
  • Comprehensive health, dental, vision, life, disability, and flexible spending benefits.
  • Retirement and savings plan with company contributions.
  • Annual discretionary bonus program and stock-based long-term incentives.
  • Paid time-off plans and career development opportunities.
  • Sponsorship for this role is not guaranteed.

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