Quality Assurance Specialist

About the role

The Quality Assurance Specialist will ensure that all manufacturing activities comply with regulatory requirements and Good Manufacturing Practices (GMP). Based on the shop‑floor in Goa, the role works closely with production teams to maintain high quality standards throughout the product lifecycle.

Key responsibilities

• Conduct regular audits of production processes and identify potential quality issues.
• Manage and resolve quality‑related incidents promptly, leading root‑cause investigations and implementing preventive actions.
• Monitor quality performance metrics, analyse data trends and drive corrective actions.
• Support internal and external audits, regulatory inspections and provide required documentation.
• Develop and execute risk‑management strategies to mitigate quality risks.
• Promote a culture of continuous improvement and quality awareness across the organization.

Required profile

• 5‑7 years of quality assurance experience in the pharmaceutical industry.
• BPharm or MPharm degree.
• Strong knowledge of GMP and quality assurance principles.
• Excellent verbal and written communication skills in English and the local language.
• Ability to work on the shop‑floor and collaborate with production teams.

Required skills

• Good Manufacturing Practices (GMP)
• Quality Assurance methodologies
• Data analysis for trend identification