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QA Specialist / Officer II (Biotechnology)

41 250 - 57 750
Формат работы
onsite
Тип работы
fulltime
Английский
b2
Страна
Netherlands
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR
QA Specialist / Officer II (Biotechnology): Supporting GMP-regulated biotechnology manufacturing through batch record review, quality event approval, and on-floor quality oversight with an accent on compliance, documentation accuracy, and cross-functional collaboration. Focus on reviewing deviations, investigations, CAPAs, change controls, and batch disposition documentation while driving quality metrics and continuous improvement.

Location: Geleen, Netherlands; fully site-based role

Salary: €41,250–€57,750 annual base pay

Company

Global life sciences organization with more than 30 sites across five continents, focused on manufacturing medicines and enabling biotechnology innovation.

What you will do

  • Provide Quality Assurance subject matter expertise to manufacturing and cross-functional stakeholders on GMP and quality activities.
  • Review batch records and prepare documentation for batch disposition within agreed timelines.
  • Review and approve deviations, investigations, CAPAs, change controls, and other quality events.
  • Review and approve SOPs, master batch records, protocols, reports, forms, and related quality documentation.
  • Provide QA oversight on the floor during manufacturing, warehouse, and quality control operations.
  • Support quality metrics, KPI reporting, quality meetings, batch documentation archiving, and product label verification.

Requirements

  • Bachelor’s or Master’s degree in Biotechnology, Life Sciences, Chemistry, or a related scientific discipline.
  • Experience in a GMP-regulated manufacturing environment, preferably in biotechnology or pharmaceutical manufacturing.
  • Experience in Quality Assurance or a related quality function, with knowledge of GMP regulations and compliance requirements.
  • Strong attention to detail and ability to identify compliance risks in technical documentation.
  • Ability to prioritize multiple activities, solve problems, and escalate issues appropriately.
  • Business-fluent English required, both written and spoken.

Culture & Benefits

  • Full-time position with competitive compensation and a comprehensive benefits package tailored to the Netherlands.
  • Career growth and development opportunities within a global life sciences organization.
  • Collaborative, inclusive, ethical workplace guided by accountability, excellence, passion, integrity, and collaboration.
  • Opportunity to work with advanced biotechnology manufacturing technologies.
  • In-person collaboration in a site-based manufacturing environment.

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