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1 день назад

Manufacturing Support Services Specialist (Cell Therapy)

28 - 38$
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 Support Services Specialist (Cell Therapy): Supporting GMP manufacturing operations and warehouse activities for an automated cell therapy manufacturing platform with an accent on aseptic processing, sample management, and controlled materials handling. Focus on operating process equipment, maintaining accurate production records, managing deviations and CAPAs, and coordinating with quality, engineering, facilities, and process teams.

Location: Bridgewater, New Jersey; on-site
Schedule: Night shift, 6:00 PM–6:00 AM

Salary: $28–$38 per hour

Company

hirify.global develops and operates integrated technologies and Smart Factories for high-throughput cell therapy manufacturing.

What you will do

  • Perform routine GMP manufacturing procedures, including buffer and media preparation, controlled-rate freezer operation, and liquid nitrogen tank handling.
  • Manage samples and transport activities using LIMS.
  • Receive, label, store, and supply warehouse consumables using SAP and label printers; operate a forklift as needed.
  • Complete cleanroom and laboratory activities, including gowning, cleaning, restocking, consumables and PPE ordering, and equipment maintenance or qualification.
  • Revise and create production records and SOPs, review batch documentation, and support deviation and CAPA closure.
  • Train new associates and collaborate with Quality Control, Facilities, Materials Management, Quality Assurance, Validation, engineering, and process teams.

Requirements

  • Bachelor’s degree or diploma in a scientific or related field is preferred.
  • 1–2 years of experience in biotech or biopharma cGMP operations, preferably in cell and gene therapy.
  • Experience following protocols, SOPs, batch records, and other GMP documentation.
  • Proficiency with drug product-related process equipment; SAP and LIMS experience is preferred.
  • Strong analytical, problem-solving, written, verbal, presentation, and interpersonal skills.
  • Ability to work on-site in Bridgewater, New Jersey, work the night shift, and lift 30 pounds. Compliance with cGMP and company safety procedures is required.

Culture & Benefits

  • Hands-on work in a fast-paced, mission-driven, rapidly evolving organization.
  • Opportunity to contribute to technologies intended to expand access to life-saving cell therapies.
  • Required training in safety, GMP procedures, equipment, aseptic techniques, and troubleshooting.
  • Work alongside multidisciplinary teams supporting integrated manufacturing operations.

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