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Posted 12 months ago

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Quality Assurance Specialist

6th of October CityOn-siteFull-time

AI Summary

Quality Assurance Specialist at Eva Pharma implements GMP/GDP/compliance controls, reviews batch records, and participates in CAPA investigations to ensure manufacturing and packaging meet quality standards.

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 Pharmaceutical Sciences or 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

Batch Record ReviewBatch RecordsCAPACGMPChange ControlCorrective And Preventive ActionsData IntegrityDeviations ReportingEnvironmental MonitoringGDPGDP LogbooksGMPGMP ComplianceISO 9001LogbooksNon-conformities TrackingQuality Documentation SystemsRaw Material DispensingRoot-cause AnalysisSafety ProgramsSOPsStatistical ConceptsTemperature Humidity Pressure DifferentialsValidation Principles

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