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4 дня назад

Quality Control PCU Manager (Pharmaceutical)

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
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
Quality Control PCU Manager (Pharmaceutical) (GMP/QC laboratory): Managing day-to-day quality control laboratory operations at a pharmaceutical manufacturing site with an accent on GMP compliance, analytical testing, staff development, and product release support. Focus on leading investigations, CAPAs, method validation, equipment qualification, and continuous improvement across laboratory operations.

Location: City of Singapore

Company

hirify.global is developing the Singapore Modulus site as a new modular, adaptable, and technology-enabled pharmaceutical manufacturing facility.

What you will do

  • Oversee daily Quality Control laboratory operations, testing schedules, sample testing, and analytical result review.
  • Ensure compliance with GMP, internal quality standards, procedures, and regulatory requirements.
  • Lead, coach, and develop laboratory staff while maintaining training and qualification records.
  • Support analytical method validation and transfer, product batch release, equipment qualification, maintenance, and calibration.
  • Lead investigations into QC events, atypical results, deviations, change controls, and CAPAs, including root-cause analysis and remediation.
  • Support regulatory inspections and internal or external audits and drive quality, safety, operational excellence, and continuous improvement.

Requirements

  • Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology, Life Sciences, Technology, or a related discipline.
  • At least 3 years of relevant Quality Control laboratory experience in the pharmaceutical or biotechnology industry.
  • Experience managing or leading a laboratory team.
  • Good working knowledge of GMP, laboratory quality systems, and applicable regulatory requirements.
  • Strong analytical, problem-solving, organisational, communication, and people-management skills.
  • Experience with manufacturing operations, product release, investigations, CAPAs, or regulatory inspections is advantageous.

Culture & Benefits

  • Work in a manufacturing site focused on modular, adaptable, and agile pharmaceutical production.
  • Collaborate with Quality, Manufacturing, MSAT, Engineering, and other cross-functional teams.
  • Contribute to a culture of quality, compliance, safety, and continuous improvement.
  • Equal-opportunity workplace supporting people from diverse backgrounds.

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