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2 дня назад

Manager, Upstream Pilot Plant (Gene Therapy)

124 000 - 161 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
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
Manager, Upstream Pilot Plant (Gene Therapy): Executing and supporting upstream bioprocessing for high-quality gene therapy products with an accent on mammalian or microbial cell culture, bioreactor operations, aseptic processing, and cGMP documentation. Focus on scaling cell culture processes, maintaining facility readiness, supporting manufacturing investigations, and managing technology transfer and quality records.

Location: San Diego, California, United States; full-time, in-person presence required.

Salary: $124,000–$161,000 annual.

Company

hirify.global is a global biopharmaceutical company developing products for patients with serious and rare diseases.

What you will do

  • Execute upstream processes including cell culture expansion, seed train operations, bench-, pilot-, and production-scale bioreactor operations, and media/buffer preparation.
  • Operate and maintain wave/rocking platforms, stirred-tank bioreactors, incubators, and automated control systems.
  • Prepare, sterilize, and manage cell culture consumables while maintaining aseptic technique.
  • Prepare, review, and maintain batch records, SOPs, logbooks, raw material specifications, technology transfer documents, and campaign reports.
  • Support facility readiness, inspections, scale-up, technology transfer, and continuous improvement initiatives.
  • Provide upstream process subject matter expertise and support manufacturing activities, investigations, and assigned deliverables.

Requirements

  • Bachelor’s degree in Biology, Chemical Engineering, Biochemistry, or a related field.
  • At least five years of experience in upstream process development or manufacturing support in bioprocessing.
  • Hands-on experience with mammalian or microbial cell culture, seed train expansion, bioreactor operations, and media/buffer preparation.
  • Knowledge and application of current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP).
  • Experience with manufacturing investigations, root cause analysis, and deviation resolution in biologics production.
  • Ability to work full-time in person at the San Diego office.

Nice to have

  • Experience conducting manufacturing investigations in biologics or cell-culture-based production.

Culture & Benefits

  • Purpose-driven environment focused on serious and rare diseases and meaningful scientific progress.
  • Medical, dental, vision, and mental health support, plus annual wellbeing reimbursement and an Employee Assistance Program.
  • Paid time off, fertility and family-forming benefits, caregiver support, and flexible schedules with purposeful in-person collaboration.
  • 401(k) with company match, annual equity awards, ESPP, and company-paid life and disability insurance.
  • Learning resources, workshops, leadership programs, mentoring, employee resource groups, and service opportunities.

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