Quality Assurance Associate

Drlogy; Jammu district; On-site; INR 300,000 - 600,000; Full time

Job summary

Drlogy is seeking a Quality Assurance Associate in Jammu, India, to support QA operations and ensure compliance with GMP, SOPs, and batch documentation. The role involves reviewing records, conducting shop-floor checks, and supporting quality assurance activities across manufacturing processes.

The ideal candidate should possess strong documentation skills, quality awareness, and the ability to maintain compliance in a regulated pharmaceutical environment. Join a team dedicated to promoting quality culture and excellence.

Qualifications

• Strong documentation skills required.
• Quality awareness is essential.
• Ability to maintain compliance in a regulated environment.

Responsibilities

• Review batch manufacturing and quality documents for completeness.
• Ensure compliance with GMP, SOPs, and regulatory guidelines.
• Conduct shop-floor checks in manufacturing and quality areas.
• Support line clearance and in-process quality checks.
• Monitor closure of quality observations and compliance trackers.
• Assist in deviations and CAPA documentation.
• Coordinate QA activities with production and QC teams.
• Prepare QA reports and compliance summaries.

Skills

Documentation skills

Quality awareness

Compliance maintenance

Job description

Quality Assurance Associate

The Quality Assurance Associate will support QA operations by ensuring compliance with GMP, SOPs, batch documentation, shop‑floor practices, and internal quality systems. This involves batch record review, line clearance support, deviation documentation, CAPA tracking, and coordination with production, QC, warehouse, and engineering teams. The candidate should have strong documentation skills, quality awareness, and the ability to maintain compliance in a regulated pharmaceutical manufacturing environment.

Key Responsibilities

• Review batch manufacturing records, batch packing records, logbooks, and quality documents for completeness.
• Ensure compliance with GMP, SOPs, regulatory guidelines, and internal quality standards.
• Conduct shop‑floor checks in manufacturing, packing, warehouse, and quality areas.
• Support line clearance, in‑process quality checks, and process compliance verification.
• Assist in documentation related to deviations, CAPA, change control, incidents, and investigations.
• Monitor closure of quality observations, pending actions, and compliance trackers.
• Coordinate with production, QC, warehouse, and engineering teams for QA‑related activities.
• Maintain controlled documents, issuance records, retrieval logs, and archival files.
• Verify cleaning records, equipment status, material status, and area readiness when required.
• Identify documentation gaps, procedural non‑compliances, and quality risks.
• Support internal audits, customer audits, regulatory inspections, and audit readiness activities.
• Ensure data integrity, traceability, and timely completion of QA documentation.
• Participate in SOP review, training coordination, and quality improvement activities.
• Prepare QA reports, compliance summaries, and routine quality updates for reporting managers.
• Promote quality culture through regular monitoring, guidance, and adherence to approved procedures.