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18 часов назад

Quality Control System Supervisor (Pharmaceutical)

54 800 - 73 067
Формат работы
hybrid
Тип работы
fulltime
Английский
b2
Страна
Ireland
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 System Supervisor (Pharmaceutical): Overseeing quality control processes, digital solutions, documentation, data management, and end-user support in pharmaceutical QC laboratories with an accent on GMP compliance, regulatory requirements, and continuous improvement. Focus on investigating quality events, implementing remediation and CAPA actions, supporting audits and inspections, and maintaining local QC systems.

Location: Waterford, Ireland; hybrid arrangement with 3 days on-site and 2 days working from home

Salary: €54,800–€73,067 per year

Company

hirify.global is an R&D-driven, AI-powered biopharmaceutical company developing medicines and vaccines.

What you will do

  • Oversee quality control processes and digital solutions in compliance with global processes, quality tools, and regulatory requirements.
  • Issue, approve, implement, maintain, and archive local QC procedures, templates, documentation, and digital system records.
  • Manage QC digital solutions, including data and end-user management, training, and operational support.
  • Investigate quality events, issues, and discrepancies, and implement remediation actions and CAPAs.
  • Support regulatory inspections and audits by presenting QC processes, documents, and records.
  • Lead continuous improvement initiatives and represent the site in global communities of practice and quality processes.

Requirements

  • Demonstrable quality control experience in the pharmaceutical industry.
  • Knowledge of Good Manufacturing Practices (GMP) and regulatory requirements.
  • A third-level degree in science or a related discipline, or relevant experience combined with a lower-level scientific qualification.
  • Ability to analyze complex data and laboratory results and identify improvement opportunities.
  • Strong attention to detail and ability to identify and resolve quality control issues.
  • Ability to work on-site in Waterford 3 days per week.

Culture & Benefits

  • Work on medicines and vaccines that improve people’s lives worldwide.
  • Contribute to technology-enabled manufacturing and supply operations.
  • Participate in initiatives supporting more than 30 new product launches by 2030.
  • Access company employee benefit programs, subject to eligibility.

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