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2 дня назад

Production Manager (Pharmaceutical Manufacturing)

90 000 - 130 000$
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
Production Manager (Pharmaceutical Manufacturing): Leading sterile pharmaceutical manufacturing operations, production scheduling, employee development, and quality-compliant execution with an accent on cGMP, aseptic processing, cleanroom operations, and regulatory documentation. Focus on coordinating cross-functional production activities, developing frontline leaders, and maintaining safe, efficient operations through quality systems, validation, and continuous improvement.

Location: On-site in Charlottesville, Virginia; remote work is not available

Salary: $90,000–$130,000 per year

Company

Contract manufacturing organization providing small-batch sterile injectable filling, packaging, labeling, laboratory, analytical, and pharmaceutical support services from clinical trials through commercial production.

What you will do

  • Lead and manage pharmaceutical manufacturing operations, including day-to-day production activities and hands-on support when needed.
  • Supervise production leaders, coordinate manufacturing schedules with Sales and Operations, and meet customer and timeline requirements.
  • Develop, train, coach, and evaluate production employees and frontline leaders.
  • Coordinate with Quality Assurance, Facilities, and Engineering on documentation, equipment maintenance, and validation activities.
  • Write, review, and approve controlled documents, including SOPs, batch records, deviation reports, change controls, and corrective action reports.
  • Support internal audits, inspection readiness, quality compliance, and cross-functional operational improvement.

Requirements

  • Bachelor’s degree preferred, ideally in Engineering or another technical discipline.
  • Experience in pharmaceutical manufacturing or another regulated manufacturing environment, including at least three years leading and developing supervisors.
  • Strong understanding of cGMP requirements, pharmaceutical production, aseptic processing, cleanroom operations, and sterile manufacturing practices.
  • Demonstrated ability to lead, coach, and develop employees while managing multiple operational priorities.
  • Experience with Microsoft Word and Excel and the ability to learn additional database applications.
  • Regular on-site attendance is required, including extended periods in cleanroom and pharmaceutical manufacturing environments.

Nice to have

  • Leadership experience in pharmaceutical production or sterile manufacturing.
  • Experience managing deviations, non-conforming materials, change controls, corrective actions, SOPs, batch records, and regulatory or customer audits.
  • Experience coordinating equipment maintenance and validation activities.
  • Success preparing employees for increased responsibility and leadership positions.

Culture & Benefits

  • Opportunity to lead pharmaceutical manufacturing operations and influence operational effectiveness.
  • Significant responsibility for developing production employees and future frontline leaders.
  • Exposure to production planning, quality systems, validation, engineering, and cross-functional business operations.
  • Opportunities to influence training, compliance, continuous improvement, and leadership development.
  • Physical requirements include aseptic gowning qualification, extended standing, bending and reaching, close-proximity cleanroom work, and lifting up to 50 pounds.

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