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5 дней назад

Operations Supervisor (CAR-T)

96 267 - 126 351$
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
Operations Supervisor (CAR-T) (Cell Therapy Manufacturing): Directing daily production of personalized CAR-T therapies in a sterile cGMP environment with an accent on shift leadership, compliant manufacturing, and cross-functional execution. Focus on supervising production units, supporting investigations and process improvements, and resolving operational issues across Manufacturing, Engineering, and Quality.

Location: Onsite in Raritan, New Jersey, United States; assigned day or evening shift, including weekends and unplanned overtime as required.

Salary: $96,267–$126,351 USD base pay annually, plus performance-based bonus and/or equity for eligible employees.

Company

hirify.global is a global biotechnology company developing cell therapies, including CAR-T, CAR-NK, and other platforms for serious diseases.

What you will do

  • Lead multiple CAR-T process operations, including component preparation, manufacturing support, mock cell, and CAR-T production.
  • Direct shift start and wrap-up meetings, assign daily production tasks, and ensure safe, compliant execution.
  • Provide hands-on guidance on the production floor and participate in production runs when needed.
  • Support manufacturing investigations, change controls, procedures, work instructions, forms, and master batch records.
  • Partner with Manufacturing, Engineering, Quality, and external collaborators to resolve production issues.
  • Support personnel development, manufacturing projects, continuous improvement, and operational efficiency.

Requirements

  • Bachelor’s degree in Science, Engineering, or a related field, or equivalent experience.
  • At least six years of operations experience in a biotech or biopharma cGMP environment, with manufacturing, quality, or engineering experience.
  • Knowledge of cGMP regulations, FDA guidance for cell-based products, cleanroom behavior, and sterile manufacturing.
  • Strong leadership, communication, analytical, problem-solving, organizational, and cross-functional collaboration skills.
  • Proficiency with Microsoft Word, Excel, PowerPoint, and Outlook.
  • Must be authorized to work in the United States; employment eligibility is verified through E-Verify. Ability to work shifts, evenings, weekends, overtime, stand for extended periods, and lift at least 25 lbs.

Nice to have

  • Experience with Operational Excellence or Lean Manufacturing.

Culture & Benefits

  • Team-based work in a dynamic, cross-functional technical operations environment.
  • Medical, dental, and vision insurance.
  • 401(k) retirement plan with company match fully vested from day one.
  • Eight weeks of paid parental leave after three months, paid time off, sick time, holidays, and additional voluntary benefits.
  • Benefits are available exclusively to permanent full-time employees; contractors are not eligible.

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