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3 дня назад

QA Operational Pharmaceuticals (Pharmaceuticals)

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
Belgium
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 Operational Pharmaceuticals (GMP/PQRs): Supporting product and process quality within a pharmaceutical site with an accent on drafting and reviewing Product Quality Reviews (PQRs). Focus on consolidating quality data, conducting trend analysis, and ensuring strict compliance with GMP standards.

Location: Onsite at a pharmaceutical site in Belgium

Company

hirify.global is an independent technology consulting firm providing guidance and solutions to businesses across various sectors including Life Sciences and Engineering.

What you will do

  • Draft, update, and review PQRs in accordance with GMP requirements and internal procedures.
  • Collect and analyze quality data including deviations, OOS, CAPA, complaints, and QC results.
  • Perform trend analysis to identify improvement opportunities for processes and the quality system.
  • Develop and update quality documentation such as SOPs, work instructions, and templates.
  • Collaborate with Production, QC, Supply Chain, and Engineering teams to ensure data reliability.
  • Support operational QA activities including deviation management, change control, and audit preparation.

Requirements

  • Master’s, Engineering, or Pharmacist degree in pharmacy, biotechnology, chemistry, or a related field.
  • 2–4 years of experience in Quality Assurance within the pharmaceutical industry.
  • Strong knowledge of GMP and pharmaceutical quality systems.
  • Proficiency with IT tools, including Excel, quality databases, ERP, and eQMS.
  • Strong analytical mindset, attention to detail, and writing skills.

Nice to have

  • Prior experience specifically in drafting and/or reviewing PQRs.

Culture & Benefits

  • Opportunities for rapid professional growth within a fast-expanding Belgian team.
  • Exposure to prestigious projects with renowned pharmaceutical and biotechnology clients.
  • International and agile work environment that promotes intrapreneurship and meritocracy.
  • Inclusive workplace culture committed to diversity and equal opportunity.

Hiring process

  • Initial brief virtual or phone call to discuss motivations and background.
  • A series of interviews (average of 3) with line managers and team members to assess skills and fit.
  • Technical assessment or case study depending on the specific role requirements.

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