Eva Pharma

Quality Assurance Supervisor

🇪🇬 Giza, Єгипет На місці Повна зайнятість Опубліковано Тра 12, 2026
Локація Giza, Єгипет
Формат роботи На місці
Тип зайнятості Повна зайнятість
Мова English
Опубліковано 12 травня 2026 р.
Остання перевірка 28 травня 2026 р.
Контекст JobGrid

Огляд ролі від JobGrid

Quality Assurance Supervisor at Eva Pharma: Giza, Єгипет; На місці; Повна зайнятість. This listing is part of JobGrid's Вакансії QA tester з публічних сторінок кар'єри. JobGrid adds normalized role facts, source context, and a path to the employer application page so candidates can compare the listing before applying.

  • Location and workplace: Giza, Єгипет, На місці
  • Role classification: Повна зайнятість
  • Source freshness: checked by JobGrid on 2026-05-28.
  • Application path: candidates continue to the employer application page with non-personal referral tags.

Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members.

Job Summary
We are seeking a passionate and talented Quality Assurance Supervisor to join our dynamic team.

The ideal candidate will contribute to our mission of enhancing human health and well-being while ensuring compliance with the highest quality and GMP standards. The role involves supervising QA operations, supporting continuous improvement initiatives, and ensuring effective implementation of quality systems across operations.

Key Responsibilities:   

    • Provide oversight of manufacturing and packaging operations, ensuring full compliance with GMP, SOPs, and data integrity requirements, while supporting continuous improvement initiatives.
    • Review and approve batch records and logbooks, ensuring completeness, accuracy, and compliance with GDP standards.
    • Lead the handling of deviations, complaints non-conformities, and incidents, including conducting or supporting root cause investigations and ensuring effective implementation and follow-up of CAPA. 
    • Review the mutual QTAs with the company's partners.
    • Lead the handling of change control management system and follow up the relevant actions.