Quality Assurance Executive - IPQA QMS

Drlogy; Hyderabad; On-site; INR 300,000 - 500,000; Full time

Job summary

Drlogy is seeking an experienced Quality Assurance Executive to oversee in-process quality assurance and quality management system operations within pharmaceutical environments in Hyderabad, India.

This role requires a strong background in GMP compliance and the ability to monitor manufacturing activities, conduct audits, and manage complex documentation efficiently.

Ideal candidates will possess skills in CAPA handling and be adept in maintaining product quality standards.

Qualifications

• Experience in managing in-process quality assurance activities.
• Knowledge of quality management system operations.
• Adept in conducting GMP and compliance awareness training.

Responsibilities

• Monitor manufacturing activities for GMP compliance.
• Conduct line clearance before production and packaging operations.
• Perform in-process quality assurance checks regularly.
• Review batch manufacturing and quality documentation accurately.
• Manage QMS documentation and compliance activities.

Skills

GMP compliance

Documentation review

CAPA handling

Audit coordination

Product quality standards

Job description

Experienced Quality Assurance Executive - IPQA & QMS responsible for managing in-process quality assurance activities and quality management system operations within pharmaceutical manufacturing environments. Skilled in line clearance, documentation review, CAPA handling, audit coordination, and GMP compliance. Adept at maintaining product quality standards and supporting regulatory readiness initiatives.

• Monitor manufacturing activities for GMP compliance consistently.
• Conduct line clearance before production and packaging operations.
• Perform in-process quality assurance checks regularly.
• Review batch manufacturing and quality documentation accurately.
• Manage QMS documentation and compliance activities efficiently.
• Coordinate deviation, CAPA, and change control processes effectively.
• Participate in internal audits and regulatory inspection activities.
• Coordinate with production and QC teams for quality support.
• Maintain QA records and compliance documentation systematically.
• Investigate quality incidents and implement corrective actions promptly.
• Conduct GMP and compliance awareness training programs.
• Monitor environmental and operational compliance standards.
• Support risk assessment and process improvement initiatives.
• Ensure timely closure of audit observations and deviations.
• Contribute to continuous improvement and quality excellence initiatives.