QA Reviewer

Drlogy; Ahmedabad District; On-site; INR 500,000 - 1,000,000; Full time

Job summary

Drlogy is seeking an experienced QA Reviewer in Ahmedabad District, Gujarat, responsible for ensuring compliance with pharmaceutical quality standards. You will review and assess quality documents and provide support for audits and inspections.

The ideal candidate will have extensive experience in documentation review and deviation assessment, ensuring accurate batch records and operational excellence in pharmaceutical manufacturing. Join us to contribute to continuous quality improvement initiatives.

Qualifications

• Experience in reviewing pharmaceutical quality documents and compliance reports.
• Skilled in maintaining documentation accuracy in manufacturing environments.
• Adept at supporting audits and regulatory inspections.

Responsibilities

• Review batch manufacturing and packaging records accurately.
• Ensure compliance with GMP and pharmaceutical quality standards.
• Coordinate with QA, QC, and production teams effectively.

Skills

Documentation review

Deviation assessment

Audit support

Quality systems management

Job description

Experienced QA Reviewer responsible for reviewing pharmaceutical quality documents, batch records, and compliance reports to ensure adherence to GMP and regulatory standards. Skilled in documentation review, deviation assessment, audit support, and quality systems management. Adept at maintaining documentation accuracy and supporting operational excellence within pharmaceutical manufacturing environments.

• Review batch manufacturing and packaging records accurately.
• Ensure compliance with GMP and pharmaceutical quality standards.
• Verify documentation completeness and data accuracy systematically.
• Review SOPs, protocols, and quality-related documents regularly.
• Coordinate with QA, QC, and production teams effectively.
• Investigate documentation discrepancies and support corrective actions.
• Maintain QA review records and compliance documentation properly.
• Participate in audits and regulatory inspection activities.
• Ensure timely closure of document review observations and deviations.
• Support CAPA and change control documentation activities.
• Monitor adherence to documentation control procedures consistently.
• Conduct compliance checks on manufacturing and laboratory records.
• Prepare quality review summaries and compliance reports regularly.
• Maintain audit readiness and documentation integrity standards.
• Contribute to continuous improvement and quality excellence initiatives.