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Core Technician – Cell Therapy

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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Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
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TL;DR
Core Technician – Cell Therapy (Cell Therapy Manufacturing): Manufacturing clinical and commercial cell therapy products in a regulated GMP environment with an accent on aseptic processing, cleanroom operations, and accurate GMP documentation. Focus on operating cell processing equipment, maintaining contamination control, reviewing batch records, and supporting deviation investigations.

Location: On-site in Houston, Texas, United States

Compensation: Competitive hourly pay; final compensation depends on qualifications, skills, experience, and relevant knowledge.

Company

hirify.global manufactures medicines and therapies through globally connected life-sciences operations across more than 30 sites.

What you will do

  • Perform aseptic processing and cell culture manipulations for clinical and commercial cell therapy products.
  • Operate cell processing and manufacturing equipment in Grade A/B cleanroom environments according to approved SOPs.
  • Follow contamination control, containment, safety, and GMP requirements throughout manufacturing activities.
  • Complete and review GMP documentation, manufacturing batch records, and related records accurately and on time.
  • Identify and communicate deviations, troubleshoot basic equipment issues, and support process deviation investigations.
  • Collaborate with Manufacturing, Quality Assurance, Quality Control, and other site functions to meet production schedules.

Requirements

  • High school diploma or equivalent required; an associate degree in a scientific or technical discipline is preferred.
  • 1–2 years of experience with cell therapy technologies or related biopharmaceutical manufacturing in a cGMP environment.
  • Working knowledge of aseptic processing principles, cleanroom operations, cGMP requirements, and regulatory compliance.
  • Ability to read and follow SOPs, manufacturing instructions, and production schedules, and to complete GMP documentation.
  • Proficiency with Microsoft Office, including Excel; SAP and LIMS experience is desirable.
  • Ability to perform routine aseptic gowning, stand for up to 6 hours, and lift up to 50 pounds.

Nice to have

  • Associate degree in a scientific or technical discipline.
  • Experience reviewing manufacturing records.
  • Experience with SAP and LIMS.

Culture & Benefits

  • Performance-related bonus.
  • Medical, dental, and vision insurance.
  • 401(k) matching plan.
  • Life insurance and short- and long-term disability insurance.
  • Employee assistance programs and paid time off.
  • Culture centered on collaboration, accountability, excellence, passion, and integrity.

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