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Upstream/AME Manufacturing Manager, Nights (Biotech Manufacturing)

Формат работы
onsite
Тип работы
fulltime
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:
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TL;DR
Upstream/AME Manufacturing Manager, Nights (Biotech Manufacturing): Leading night-shift production operations, cell culture activities, and Agile Manufacturing Excellence across a flexible biomanufacturing facility with an accent on safety, quality, reliability, and continuous improvement. Focus on developing high-performing teams, overseeing validation and new technology implementation, and driving compliant, efficient manufacturing execution.

Location: West Greenwich, Rhode Island, United States; onsite night shift from 7 PM to 7 AM with a rotation covering 7 days per week

Company

hirify.global is a biotechnology company developing, manufacturing, and delivering medicines across oncology, inflammation, general medicine, and rare disease.

What you will do

  • Lead production operations on the manufacturing floor, including cell culture operations in a flexible manufacturing facility.
  • Lead the Agile Manufacturing Excellence team for the night shift across AR30 and AR5.
  • Drive safety, quality, reliability, efficiency, agility, innovation, and continuous improvement.
  • Oversee right-first-time execution of the production plan and manufacturing validation activities.
  • Oversee the implementation of new manufacturing technologies.
  • Build team capabilities, allocate resources, manage talent, and provide performance feedback.

Requirements

  • High school diploma or GED plus 12 years of manufacturing and operations experience; or an associate degree plus 10 years; or a bachelor's degree plus 5 years; or a master's degree plus 3 years; or a doctorate.
  • Direct people-management experience or leadership experience in teams, projects, programs, or resource allocation.
  • Experience in a cGMP or other highly regulated environment, with understanding of engineering, biological, or chemical processing.
  • Experience with Lean principles, continuous improvement, performance management, conflict resolution, and performance reviews.
  • Strong leadership, team-building, analytical problem-solving, change-management, and technical communication skills.

Nice to have

  • Bachelor's degree in life sciences or engineering.

Culture & Benefits

  • Collaborative, innovative, science-based work environment focused on serving patients.
  • Health, dental, vision, life, disability, and flexible spending benefits.
  • Retirement and savings plan with company contributions.
  • Discretionary annual bonus, stock-based long-term incentives, and award-winning time-off plans.
  • Career development opportunities and flexible work models where applicable.

Hiring process

  • Applications are accepted until a sufficient number of applications is received or a candidate is selected.
  • Sponsorship for this role is not guaranteed.

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