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7 дней назад

Sr. Associate, Manufacturing 12 Hour Shift (Evenings 6pm-6am) (Biotech)

86 048 - 116 418$
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
Sr. Associate, Manufacturing 12 Hour Shift (Evenings 6pm-6am) (Biotech): Leading device assembly and packaging operations for pharmaceutical manufacturing with an accent on cGMP compliance, equipment performance, and production support. Focus on troubleshooting automated equipment, supporting validation and CAPA activities, and driving lean manufacturing improvements.

Location: New Albany, Ohio, United States; onsite manufacturing role with a 12-hour evening shift from 6:00 p.m. to 6:00 a.m.

Salary: $86,048.05–$116,417.95 per year

Company

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

What you will do

  • Lead device assembly and packaging operations on the manufacturing floor while supporting equipment setup, operation, and troubleshooting.
  • Maintain equipment uptime, clear faults and stoppages, and ensure production schedules are completed.
  • Supervise and train manufacturing technicians on processes and equipment.
  • Maintain safety and cGMP compliance and escalate risks affecting personnel, equipment, quality, or product supply.
  • Collaborate with Quality, Engineering, Manufacturing Support, Process Development, and Regulatory Compliance teams to resolve manufacturing events.
  • Support deviations, CAPA, controlled documentation, equipment qualification and validation, and continuous improvement initiatives.

Requirements

  • High school diploma/GED plus 4 years of biotech or pharmaceutical manufacturing, process development, or quality experience; or an associate degree plus 2 years; or a bachelor's degree plus 6 months; or a master's degree.
  • Technical understanding of pharmaceutical or biotech packaging equipment and processes.
  • Experience with current Good Manufacturing Practices (cGMP), GMP operations, process development, scheduling, or GMP technical support.
  • Ability to analyze technical data, troubleshoot process and equipment issues, manage competing priorities, and work effectively in cross-functional teams.
  • Experience with commissioning and qualification, cleaning validation, new product introduction, or process performance qualification is preferred.
  • Experience with manufacturing systems such as MES, LIMS, Maximo, CCMS, or SAP is preferred.

Nice to have

  • Degree in Chemical Engineering, Industrial Engineering, or Life Sciences.
  • Background in lean manufacturing and operational excellence.
  • Experience leading cross-functional teams and supporting continuous improvement.

Culture & Benefits

  • Employee health, dental, vision, life, disability, and flexible spending benefits.
  • Retirement and savings plan with company contributions.
  • Discretionary annual bonus and stock-based long-term incentives.
  • Paid time-off programs and career development opportunities.
  • Flexible work models may be available where applicable; this manufacturing role is tied to the New Albany site.

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