Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Понятные обязанности руководителя, практическая работа с iPSC и клеточной терапией, а также описанные льготы делают вакансию привлекательной. Сменный график и круглосуточная ответственность за эскалации могут осложнить баланс работы и личной жизни.
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Смены и дежурстваБиотех с потенциаломПонятная зона ответственностиОценка зарплаты
Оценка от Hirify AI
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Supervisor, Differentiation (iPSC) (Cell Therapy/GMP): Leading Manufacturing Associates and performing hands-on iPSC culture, directed differentiation, harvesting, cryopreservation, and in-process testing in a regulated GMP cleanroom environment with an accent on aseptic processing, documentation, and operational continuity. Focus on resolving equipment and process disruptions, maintaining production targets, supporting validation and tech transfer, and developing manufacturing staff.
Location: 100% onsite in Silver Spring, Maryland, United States
Salary: $37.98–$50.48 per hour
Company
hirify.global develops pharmaceutical therapies for rare diseases and technologies intended to expand the availability of transplantable organs.
What you will do
Lead and work alongside Manufacturing Associates in iPSC culture, directed differentiation, harvesting, cryopreservation, material preparation, and in-process testing.
Ensure manufacturing activities follow phase-appropriate GMP principles, established procedures, OSHA requirements, and safety policies.
Act as the primary escalation point for production-floor operations, equipment alarms, process interruptions, deviations, and non-conformances.
Review and approve batch records, investigations, corrective actions, SOPs, and manufacturing procedures.
Plan production schedules, support ramp-up, technology transfer, operational readiness, equipment qualification, validation, and troubleshooting.
Conduct performance evaluations, provide coaching and training, and develop Manufacturing Associates.
Requirements
Bachelor’s degree in a directly related life science specialty.
At least 5 years of hands-on experience with cell culture and expansion in 2D and 3D systems, including bioreactors.
Experience with automated and closed-system cell manufacturing platforms, aseptic processing equipment, cleanroom practices, and contamination control.
Knowledge of cell therapy techniques, pharmaceutical GMPs, FDA guidelines, and relevant industry standards.
Ability to work extended periods in full gowning and on a rotating schedule that includes weekends, holidays, flexible hours, and off-shift support.
Strong technical troubleshooting, documentation, communication, cross-functional collaboration, and people-management skills.
Nice to have
At least 5 years of GMP experience and 1 year of direct supervisory experience.
Hands-on experience with stem cell differentiation, including iPSCs.
Basic understanding of quality control and in-process checks such as viability, flow cytometry, qPCR, and endotoxin testing.
Culture & Benefits
Medical, dental, vision, and prescription coverage.
Wellness resources, 401(k), and ESPP savings plans.
Paid time off, paid parental leave, and disability benefits.
Work focused on rare-disease therapies and manufactured transplantable organs.
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