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12 часов назад

Manager Quality Assurance (IQA) (Pharmaceutical Manufacturing)

Формат работы
onsite
Тип работы
fulltime
Грейд
lead
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
Manager Quality Assurance (IQA) (Pharmaceutical Manufacturing): Leading incoming material quality assurance operations at a Singapore manufacturing site with an accent on material inspection, sampling, rapid identification testing, and GMP compliance. Focus on reviewing quality records, managing deviations and CAPAs, supporting audits and inspections, and developing the IQA team.

Location: Singapore Manufacturing - Tuas

Company

hirify.global develops biological medicines and applies science and technology to treat serious illnesses.

What you will do

  • Lead and direct the Incoming Quality Assurance team within the Lot Disposition group.
  • Oversee inspection, sampling, and rapid identification testing of incoming raw materials according to specifications, SOPs, cGMP, and applicable regulations.
  • Review and approve quality processes, procedures, documents, records, nonconformances, CAPAs, change controls, protocols, and deviation investigations.
  • Monitor documentation, dashboards, metrics, inventory, equipment, and operational readiness, while supporting audits and regulatory inspections.
  • Identify quality, compliance, supply, and safety risks; troubleshoot operational issues and support continual improvement initiatives.
  • Coach, onboard, develop, and conduct performance reviews for IQA staff.

Requirements

  • Doctorate degree, or a master's degree with 2 years of relevant experience, bachelor's degree with 4 years, or diploma with 8 years in a pharmaceutical company or GMP environment.
  • At least 5 years of experience in the pharmaceutical industry.
  • Experience with laboratory and process equipment, including basic troubleshooting.
  • Experience with LIMS, SAP, and TrackWise.
  • Knowledge of chemistry, single-use materials, GMP, regulatory requirements, safety guidelines, and quality documentation.
  • Ability to lead and develop teams, solve problems cross-functionally, manage priorities, and communicate with technical staff, senior management, and inspectors.

Culture & Benefits

  • Collaborative and inclusive working environment.
  • Professional and personal development opportunities.
  • Competitive benefits supporting employee growth.
  • Medical checks required for the role are covered by the company.

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