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2 дня назад

Manufacturing Supervisor (Biopharmaceutical)

95 250 - 158 750$
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
Manufacturing Supervisor (Biopharmaceutical): Leading biopharmaceutical manufacturing shift performance and producing high-quality medicines in a fully site-based cGMP environment with an accent on compliance, productivity, and staff development. Focus on driving Lean improvements, managing deviations and investigations, coordinating validated equipment and processes, and maintaining inspection readiness.

Location: Vacaville, California, United States; fully site based. Shift hours: 6:30pm–7:30am, Wednesday–Friday and every other Saturday.

Salary: $95,250–$158,750 gross annual base salary, plus performance-related bonus.

Company

hirify.global operates biopharmaceutical manufacturing sites across five continents and produces medicines for the life sciences industry.

What you will do

  • Lead manufacturing shift performance, including budget management, productivity, labor efficiency, and operational goals.
  • Maintain cGMP compliance, inspection readiness, and production of high-quality medicines under health authority regulations and hirify.global quality systems.
  • Drive Lean manufacturing and continuous improvement initiatives to improve efficiency, quality, and operational performance.
  • Lead, train, and develop manufacturing staff to ensure qualification, accountability, and strong team performance.
  • Oversee manufacturing equipment, facilities, and validated processes while coordinating maintenance and technical improvements.
  • Manage deviations, investigations, validation strategies, and technical transfers, implementing sustainable corrective and preventive actions.

Requirements

  • AS, BS, or BA in Biological Sciences, Physical Sciences, or Engineering preferred.
  • 5–6 years of supervisory experience in biotechnology, pharmaceuticals, or a related industry preferred.
  • Experience ensuring safe, compliant, and efficient operations in large-scale cGMP manufacturing.
  • Experience leading cGMP-compliant operations through health authority inspections.
  • Ability to lead and develop operational staff in a dynamic manufacturing environment.
  • Background in aseptic and bioprocessing technologies and experience with Lean methods are preferred.

Culture & Benefits

  • In-person collaboration in a fully site-based manufacturing environment.
  • Performance-related bonus.
  • Medical, dental, and vision insurance.
  • 401(k) matching, life insurance, and short- and long-term disability insurance.
  • Employee assistance programs and paid time off.
  • Work culture centered on collaboration, accountability, excellence, passion, and integrity.

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