QMS Executive

Drlogy; Mumbai; On-site; INR 600,000 - 800,000; Full time

Job summary

Drlogy seeks an experienced QMS Executive to manage quality management system activities and ensure GMP compliance in pharmaceutical environments. Key responsibilities include maintaining documentation, coordinating CAPA activities, and supporting quality operations.

The ideal candidate will effectively monitor quality KPIs, facilitate GMP training, and ensure audit readiness. This position offers a chance to contribute to operational excellence initiatives within a dynamic team.

Qualifications

• Experienced in managing quality management systems in manufacturing environments.
• Skilled in ensuring compliance with GMP standards.
• Adept at documentation control and maintaining audit readiness.

Responsibilities

• Manage quality management system operations and compliance activities.
• Ensure adherence to GMP and pharmaceutical quality standards.
• Review SOPs, batch records, and quality documents systematically.

Skills

Documentation control

CAPA handling

Audit coordination

Compliance monitoring

Quality systems administration

Job description

Experienced QMS Executive responsible for managing quality management system activities, ensuring GMP compliance, and supporting pharmaceutical quality operations within manufacturing environments. Skilled in documentation control, CAPA handling, audit coordination, compliance monitoring, and quality systems administration. Adept at maintaining regulatory readiness and operational quality standards.

Responsibilities

• Manage quality management system operations and compliance activities.
• Ensure adherence to GMP and pharmaceutical quality standards.
• Maintain QMS records and compliance documentation accurately.
• Coordinate deviation, CAPA, and change control activities effectively.
• Review SOPs, batch records, and quality documents systematically.
• Participate in internal audits and regulatory inspection activities.
• Coordinate with QA, QC, and production teams efficiently.
• Investigate quality incidents and implement corrective actions.
• Monitor implementation of quality systems across departments.
• Conduct GMP and compliance awareness training programs.
• Ensure timely closure of audit observations and deviations.
• Support risk assessment and process improvement initiatives.
• Monitor quality KPIs and operational compliance metrics.
• Maintain audit readiness and documentation control standards.
• Contribute to continuous improvement and operational excellence initiatives.