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18 часов назад

Quality Control Analytical Expert (Pharmaceutical Quality Control)

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 Analytical Expert (Pharmaceutical Quality Control): Supporting analytical method validation, transfers, troubleshooting, investigations, and QC operations in a pharmaceutical manufacturing environment with an accent on cGMP compliance, data integrity, and analytical method performance. Focus on coordinating validation and transfer testing, writing protocols and reports, analyzing trends, and resolving complex laboratory quality issues.

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

Salary: €54,800–€73,067 per year.

Company

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

What you will do

  • Provide analytical expertise for method validation, transfers, troubleshooting, investigations, and laboratory technologies.
  • Coordinate analytical testing for validation and transfer projects against committed schedules.
  • Write, review, and maintain protocols, reports, analytical methods, and related procedures.
  • Perform trend analysis of method performance to determine when methods should be revalidated, optimized, or replaced.
  • Maintain laboratory facilities and instruments in an appropriate quality and safety condition.
  • Support QC teams during internal and external audits and inspections.

Requirements

  • Significant quality control experience in the pharmaceutical industry.
  • Knowledge of Good Manufacturing Practices, cGMP, and regulatory requirements.
  • Third-level qualification in science or a related discipline, or relevant experience supplementing a lower-grade 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 follow HSE requirements and maintain accurate raw data, calculations, records, and data integrity documentation.

Culture & Benefits

  • Work on medicines and vaccines intended to improve lives worldwide.
  • Contribute to technology-enabled manufacturing and supply operations.
  • Participate in a workplace focused on inclusion, equal opportunity, and continuous improvement.
  • Company employee benefit programs may be available.
  • 12-month fixed-term contract with a hybrid working arrangement.

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