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Manager, Upstream Pilot Plant (Biotechnology)

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 (Biotechnology): Executing upstream processes for gene therapy products, including cell culture expansion, bioreactor operations, and media and buffer preparation with an accent on cGMP/GDP compliance, documentation, and viral vector manufacturing. Focus on operating pilot-scale equipment, supporting investigations and root cause analysis, and enabling scale-up and technology transfer.

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 focused on transforming the lives of patients with serious and rare diseases.

What you will do

  • Execute upstream processes including cell culture expansion, bench-, pilot-, and production-scale bioreactor operations, and media and buffer preparation.
  • Operate and maintain wave or rocking platforms, stirred-tank bioreactors, incubators, and automated control systems.
  • Prepare and sterilize cell culture consumables while maintaining aseptic technique.
  • Prepare, review, and maintain batch records, SOPs, logbooks, material specifications, technology transfer documents, and campaign reports.
  • Support cGMP/GDP compliance, facility readiness, inspections, quality systems, ERP tracking, and continuous improvement initiatives.
  • Provide upstream process expertise, own assigned deliverables, and support manufacturing investigations and deviation resolution.

Requirements

  • Bachelor’s degree in Biology, Chemical Engineering, or Biochemistry.
  • At least 5 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 or buffer preparation.
  • Knowledge and application of current Good Manufacturing Practices and Good Documentation Practices.
  • Experience collaborating cross-functionally and supporting investigations, root cause analysis, and deviation resolution in biologics production.
  • Familiarity with quality systems, ERP platforms, and electronic documentation systems.

Nice to have

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

Culture & Benefits

  • Purpose-driven environment focused on patients with serious and rare diseases.
  • Medical, dental, vision, and mental health coverage, plus annual wellbeing reimbursement and EAP access.
  • Paid time off, fertility and family-forming benefits, caregiver support, and flexible schedules with purposeful in-person collaboration.
  • 401(k) match, annual equity awards, ESPP participation, and company-paid life and disability insurance.
  • Learning programs, mentorship, employee resource groups, service programs, and recognition opportunities.

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