Quality Associate

We are seeking a motivated and detail-oriented fresh graduate to join our Quality team as a Quality Associate. This role offers hands-on training and exposure to pharmaceutical quality systems, ensuring compliance with Good Manufacturing Practices (GMP), regulatory standards, and company policies. The Quality Associate will assist in routine quality assurance activities, documentation control, audits, and continuous improvement initiatives to support the delivery of safe and effective products.

Key Responsibilities :

• Assist in reviewing and maintaining quality documents such as SOPs, batch records, and deviation reports.
• Support the implementation and monitoring of Good Manufacturing Practices (GMP) across production and laboratory areas.
• Participate in internal audits, inspections, and quality system reviews.
• Help track, record, and follow up on deviations, CAPAs (Corrective and Preventive Actions), and change controls.
• Conduct basic quality checks and verification of raw materials, in-process, and finished products as per procedures.
• Assist with training activities and awareness programs related to quality and compliance.
• Collaborate with cross-functional teams (Production, QC, Regulatory Affairs, Supply Chain) to resolve quality-related issues.
• Contribute to continuous improvement initiatives to strengthen compliance and efficiency.