Vaccine QA Specialist

EVA Pharma

Responsibilities:

• Monitor environmental conditions (temperature, humidity, pressure differentials) across vaccine production and storage areas, ensuring compliance with GMP requirements.
• Participate in raw material dispensing for vaccine manufacturing and verify specifications and calculations as per SOPs.
• Oversee vaccine manufacturing and packaging operations to ensure adherence to GMP, SOPs, and data integrity requirements.
• Review batch records and logbooks related to vaccine production for completeness, accuracy, and compliance with GDP.
• Record and report deviations, non-conformities, and incidents specific to vaccine processes. Participate in root cause investigations and track corrective and preventive actions (CAPA).

• Bachelor s degree in Pharmacy.
• 0 2 years of relevant experience in pharmaceutical QA; experience in vaccine manufacturing is a plus.
• 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.