Qualifications and Skills

• Bachelor's degree in Pharmacy, Chemistry,
• 4 to 6 years of experience in pharmaceutical quality assurance.
• Strong knowledge of quality systems and regulatory requirements, including WHO-GMP.
• Experience in conducting quality audits and inspections.
• Excellent attention to detail and analytical skills.
• Effective communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Proficient in MS Office applications.
• Knowledge of relevant software for quality documentation and data analysis is a plus.
• Knowledge of Good Laboratory Practices (GLP) and Good Documentation Practices (GDP) is desirable.

Roles and Responsibilities

• Ensure compliance with quality standards and regulatory requirements throughout the manufacturing process.
• Conduct quality checks and inspections at various stages of production to identify any deviations or non-conformities.
• Create and maintain quality documentation, including standard operating procedures (SOPs), batch records, and testing records.
• Monitor and analyze quality data to identify trends, opportunities for improvement, and potential risks.
• Assist in the investigation of customer complaints and the implementation of effective corrective actions.