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4 часа назад

Validation/Qualification Officer (Pharmaceutical Quality Assurance)

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
Morocco
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
Validation/Qualification Officer (Pharmaceutical Quality Assurance): Developing and maintaining qualification and validation strategies for pharmaceutical equipment, utilities, and processes with an accent on GMP documentation, cleaning validation, and quality systems. Focus on coordinating validation activities, investigating anomalies, and managing deviations, change controls, and CAPA through closure.

Location: El Jadida, Morocco; on-premise

Company

hirify.global operates in the pharmaceutical industry, delivering products under science- and risk-based quality standards.

What you will do

  • Develop and maintain qualification and validation strategies and support the Site Validation Master Plan.
  • Prepare, execute, review, and maintain qualification and validation protocols, reports, schedules, and GMP documentation.
  • Coordinate cleaning validation, process validation, and holding-time validation activities.
  • Participate in equipment and utility requalification, qualified-state assessments, and investigations of validation anomalies.
  • Support deviation, change control, and CAPA processes, including impact assessments and effectiveness follow-up.
  • Monitor quality KPIs, support compliance and continuous-improvement initiatives, and act as backup for the Quality System Specialist.

Requirements

  • Pharmacist, master's degree, or equivalent qualification in Pharmacy, Pharmaceutical Sciences, Biotechnology, Chemical Engineering, Quality Assurance, or a related scientific discipline.
  • At least 3 years of experience in the pharmaceutical industry and Quality Assurance.
  • Sound knowledge of current Good Manufacturing Practices (GMP) within GxP.
  • Effective written and oral communication skills.
  • Ability to work effectively within interdepartmental teams.

Nice to have

  • Experience at a manufacturing site and in qualification, validation, deviation management, change control, CAPA management, and GMP documentation.
  • Specialization in Pharmaceutical Quality Assurance.
  • Experience supporting continuous improvement and GMP training initiatives.
  • Problem-solving, independent working, time-management, and multitasking skills.
  • Experience using generative AI tools such as ChatGPT or Microsoft Copilot.

Culture & Benefits

  • Work is performed on premise in El Jadida, Morocco.
  • Quality activities are guided by science, risk-based compliance, and continuous improvement.
  • The role contributes directly to product quality and patient safety.

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