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22 часа назад

Operations Manager (2nd Shift)

127 313 - 167 099$
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 Manager (2nd Shift) (Cell Therapy Manufacturing): Overseeing personalized cell therapy production for clinical and commercial requirements in a sterile cGMP environment with an accent on compliant manufacturing, staff leadership, and production scheduling. Focus on managing investigations and change controls, maintaining inspection readiness, coordinating cross-functional operations, and driving continuous improvement across multiple work centers.

Location: Onsite in Raritan, New Jersey, United States; Monday to Friday on the 2nd shift, with overtime and weekends as required.

Salary: $127,313–$167,099 USD per year, plus performance-based bonus and/or equity for eligible roles.

Company

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

What you will do

  • Oversee personalized cell therapy production in a sterile cGMP environment for clinical and commercial supply.
  • Lead 2nd-shift operations, assign personnel to daily production schedules, and manage hiring, development, and performance.
  • Manage multiple work centers, production metrics, operational procedures, manufacturing work instructions, batch records, and forms.
  • Support manufacturing investigations, change controls, regulatory inspections, and ongoing inspection readiness.
  • Partner with Manufacturing, Engineering, Quality, and external stakeholders to execute production schedules and projects.
  • Lead facility operating reviews and department projects focused on continuous improvement and operational efficiency.

Requirements

  • Bachelor’s degree in Engineering or a related field, or equivalent experience.
  • At least 5 years of operations experience in a cGMP biotech or biopharma environment, including at least 3 years of supervisory experience.
  • Strong knowledge of GMP compliance and FDA, EMA, and other global pharmaceutical manufacturing requirements.
  • Ability to manage shifting priorities, multiple tasks, cross-functional issues, and critical deadlines in a fast-paced environment.
  • Strong analytical, problem-solving, critical-thinking, communication, and people-leadership skills.
  • Must be authorized to work in the United States; employment eligibility is verified through Form I-9 and E-Verify.

Nice to have

  • Cell or gene therapy experience.
  • Experience with Operational Excellence or Lean Manufacturing.
  • Familiarity with manufacturing systems such as MES and ERP, and with digital transformation initiatives.

Culture & Benefits

  • Medical, dental, and vision insurance with a 401(k) plan and company match fully vested on day one.
  • Eight weeks of paid parental leave after three months of employment.
  • Paid vacation, personal and sick time, floating holidays, and eleven company holidays.
  • Additional benefits include flexible spending and health savings accounts, insurance programs, commuter benefits, family-care resources, and well-being initiatives.
  • Benefits are available exclusively to permanent full-time employees; contractors are not eligible.

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