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5 дней назад

Associate Manufacturing Nights (Biotechnology)

Формат работы
onsite
Тип работы
fulltime
Грейд
junior
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
Associate Manufacturing Nights (Biotechnology) (GMP/biomanufacturing): Performing high-volume manufacturing operations in biotechnology facilities with an accent on aseptic processing, critical process monitoring, documentation, and production equipment troubleshooting. Focus on executing SOPs during rotating 12-hour night shifts, managing deviations and CAPA improvements, and maintaining inspection-ready manufacturing areas.

Location: West Greenwich, Rhode Island, United States; onsite manufacturing facilities. The role works rotating 12-hour night shifts from 7 PM to 7 AM, averaging 14 shift days per month, with every other weekend off. Initial onboarding lasts 2–6 weeks on an administrative Monday–Friday schedule, approximately 8 AM–5 PM.

Company

hirify.global is a biotechnology company researching, manufacturing, and delivering medicines for serious diseases across oncology, inflammation, general medicine, and rare disease.

What you will do

  • Perform high-volume manufacturing operations according to standard operating procedures.
  • Operate in laminar flow hoods and monitor critical manufacturing processes.
  • Complete validation protocols and draft or revise manufacturing procedures, SOPs, and technical reports.
  • Conduct basic troubleshooting, review documentation, and own deviations where assigned.
  • Support cross-functional teams and implement CAPA and continuous improvement initiatives.
  • Maintain inspection-ready workspaces, organize inventory, and use Delta V and electronic batch record systems.

Requirements

  • High school diploma/GED plus 2 years of manufacturing or operations experience, or an associate degree plus 6 months of relevant experience, or a bachelor’s degree in a related field.
  • Ability to work the rotating 12-hour night schedule and complete the weekday onboarding schedule.
  • Knowledge of GMP principles, manufacturing documentation, basic statistics, and production equipment troubleshooting.
  • Ability to understand and apply basic chemistry, biology, and physical principles.
  • Technical writing, documentation review, teamwork, and communication skills.

Nice to have

  • Bachelor’s degree in science or engineering.
  • Experience with biotechnology operations such as purification, cell culture, aseptic processing, or single-use systems.
  • Experience with CFR and regulatory requirements, Delta V, laboratory equipment, or manufacturing testing.
  • Mechanical ability, project management, and presentation skills.

Culture & Benefits

  • Collaborative, innovative, science-based work environment focused on patient care.
  • 15% night-shift differential and premium pay for Sundays worked.
  • Health, dental, vision, life, disability, and flexible spending benefits for eligible employees and dependents.
  • Retirement and savings plan with company contributions, annual bonus eligibility, and stock-based long-term incentives.
  • Paid time off, career development opportunities, and flexible work models where applicable.

Hiring process

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

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