Назад
Company hidden
4 часа назад

Operations Support Specialist (Cell Therapy)

47 861 - 62 819$
Формат работы
onsite
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Operations Support Specialist (Cell Therapy): Performing sterile cGMP process operations for personalized CAR-T cell therapy production with an accent on cell culture, purification, aseptic processing, and cryopreservation. Focus on executing batch records, handling biological materials and hazardous chemicals, and driving manufacturing process improvements across cross-functional Technical Operations teams.

Location: Onsite in Raritan, New Jersey, United States; assigned production shift schedule, including evenings and weekends as required.

Salary: $47,861–$62,819 USD per year, plus potential performance-based bonus and/or equity for eligible roles.

Company

hirify.global is a biotechnology company developing cell therapies, including CAR-T, TCR-T, and natural killer cell-based therapies, for serious diseases.

What you will do

  • Perform cell culture, purification, aseptic processing, and cryopreservation according to standard operating procedures and batch records.
  • Record production data accurately and complete manufacturing tasks according to shift schedules.
  • Follow safety policies, quality systems, and cGMP requirements in a sterile production environment.
  • Collaborate with Manufacturing, Engineering, Quality, and external partners on production activities.
  • Support manufacturing process development, continuous improvement, and operational efficiency initiatives.
  • Handle biological materials and hazardous chemicals in a BSL-2 cleanroom facility.

Requirements

  • Bachelor’s degree in engineering or a related field, or equivalent experience.
  • 0–1 years of operations experience in a cGMP biotech or biopharma environment.
  • Knowledge of cGMP regulations and FDA guidance for manufacturing cell-based products.
  • Ability to work independently, prioritize multiple tasks, integrate cross-functional issues, and communicate clearly.
  • Ability to handle human-derived materials in a BSL-2 cleanroom, lift at least 50 lbs, and stand for extended periods.
  • Must be authorized to work in the United States; employment eligibility is verified through Form I-9 and E-Verify. Ability to accommodate unplanned overtime with little or no notice is required.

Culture & Benefits

  • Permanent full-time employees receive medical, dental, and vision insurance.
  • 401(k) retirement plan with a company match that fully vests on day one.
  • Eight weeks of paid parental leave after three months of employment.
  • Paid vacation, personal time, sick time, floating holidays, and eleven company holidays.
  • Additional benefits include flexible spending and health savings accounts, disability coverage, legal assistance, commuter benefits, family care resources, and well-being programs.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →