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Posted 7 months ago

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Quality Assurance Specialist

GizaOn-siteFull-time

AI Summary

Quality Assurance Specialist at Eva Pharma ensuring GMP/GDP compliance, batch review, CAPA tracking, and supporting QA operations.

About this role

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 Specialist to join our dynamic team.

The ideal candidate will contribute to our mission of enhancing human health and well-being, ensuring that we meet the highest standards of excellence in our industry.

Responsibilities:

  • Monitor environmental conditions (temperature, humidity, pressure differentials) and ensure they comply with GMP requirements across production and warehouse areas

  • Participate in raw material dispensing and verify specifications and calculations as per SOPs

  • Oversee manufacturing and packaging operations to ensure adherence to GMP, SOPs, and data integrity requirements

  • Review batch records and logbooks for completeness, accuracy, and compliance with GDP (Good Documentation Practice)

  • Record and report deviations, non-conformities, and incidents. Participate in root cause investigations and track corrective and preventive actions (CAPA)

Requirements

  • Bachelor's degree in Pharmacy.

  • 0-2 years of relevant experience in a pharmaceutical QA environment

  • Knowledge of cGMP and GDP principles

  • Understanding of CAPA, change control, and quality documentation systems

  • Familiarity with ISO 9001 and safety programs

  • Awareness of validation principles and basic statistical concepts

Skills

Basic StatisticsBatch RecordsCAPACGMPChange ControlCorrective And Preventive ActionsData IntegrityDeviation HandlingEnvironmental MonitoringGDPGMPGxPISO 9001LogbooksManufacturing And Packaging OperationsNon-conformitiesQA In Pharmaceutical ManufacturingQuality Documentation SystemsRoot Cause InvestigationSOPsValidation Principles

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