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1 день назад

QC Manager, Microbiology

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Singapore
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
QC Manager, Microbiology (Pharmaceutical Manufacturing): Establishing and operating a state-of-the-art microbiology QC laboratory at a new Singapore site with an accent on cGMP compliance, microbiological testing, and team leadership. Focus on validating laboratory systems, resolving OOS results and deviations, supporting batch release and inspections, and driving continuous improvement.

Location: Tuas, Singapore; onsite role at a new manufacturing facility

Company

hirify.global develops and manufactures healthcare solutions, including vaccines and biological products, through a global industrial network.

What you will do

  • Lead the day-to-day operations of the QC microbiology team and ensure compliance with cGMP, HSE, and regulatory requirements.
  • Plan, execute, and improve microbiological testing, including bioburden, endotoxin, environmental monitoring, and water testing.
  • Coach and develop QC analysts while monitoring quality, safety, and productivity KPIs.
  • Investigate and resolve Out-of-Specification results, deviations, and CAPAs.
  • Collaborate with Manufacturing, Quality Assurance, and Regulatory Affairs on batch release and regulatory submissions.
  • Ensure laboratory equipment, methods, and systems are qualified, validated, maintained, and inspection-ready.

Requirements

  • Degree in Microbiology, Life Sciences, or a related scientific discipline.
  • Approximately 10–12 years of experience in a pharmaceutical or biopharmaceutical microbiology laboratory.
  • Experience managing people and working collaboratively in a fast-paced environment.
  • Strong knowledge of microbiological testing methods, EU/US cGMP regulations, and quality management systems.
  • Experience with quality management, risk-based approaches, operational excellence, and safety management.
  • Proficiency in English and availability to work onsite in Singapore.

Culture & Benefits

  • Opportunity to support the start-up of a new, fully digitalized Modulus manufacturing facility.
  • Work across vaccine and biological platforms, including mRNA.
  • Collaboration with cross-functional Manufacturing, Quality Assurance, and Regulatory Affairs teams.
  • Focus on operational excellence, continuous improvement, safety, and regulatory compliance.

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