Quality Assurance Officer

Drlogy; Hyderabad; On-site; INR 500,000 - 700,000; Full time

Job summary

Drlogy in Hyderabad is seeking a Quality Assurance Officer to support QA operations and ensure compliance with GMP and SOPs. The role includes documentation review, batch record verification, and supporting audits.

The ideal candidate will have a B.Sc, M.Sc, or B.Pharm qualification and 2–10 years of relevant experience in pharmaceutical quality. Strong knowledge of regulatory expectations and documentation control is essential.

Qualifications

• Minimum 2–10 years of experience in quality assurance.
• Strong knowledge of GMP, SOPs, and compliance practices.
• Experience in documentation review and quality systems.

Responsibilities

• Support QA operations and documentation review.
• Ensure compliance with GMP and SOPs.
• Coordinate QA requirements with cross-functional teams.
• Conduct internal and regulatory audits.

Skills

Pharmaceutical quality systems

Regulatory compliance

Documentation control

GMP knowledge

Education

B.Sc, M.Sc, or B.Pharm

Job description

The Quality Assurance Officer will be responsible for supporting QA operations, documentation review, batch record verification, deviation handling, change control, audit support, and GMP compliance in the Quality Assurance department. This requires B.Sc, M.Sc, or B.Pharm qualification with 2–10 years of experience, knowledge of pharma quality systems, regulatory expectations, documentation control, and manufacturing compliance.

• Review batch manufacturing records, batch packing records, logbooks, and quality documents.
• Ensure production, QC, warehouse, and engineering activities comply with GMP and SOPs.
• Support deviation, incident, change control, CAPA, OOS, and investigation documentation.
• Perform line clearance, in-process checks, and shop-floor compliance monitoring when assigned.
• Coordinate with production, QC, engineering, warehouse, and regulatory teams for QA requirements.
• Maintain QA documentation, SOPs, formats, registers, and controlled records.
• Support internal audits, vendor audits, regulatory audits, and compliance readiness.
• Verify cleaning records, equipment records, area records, and process documentation.
• Review validation, qualification, stability, and product quality-related documents.
• Identify compliance gaps and recommend corrective and preventive actions.
• Ensure data integrity, documentation accuracy, and timely closure of quality records.
• Train employees on GMP, GDP, SOPs, hygiene, and quality compliance practices.
• Support product release activities and quality review processes under senior guidance.
• Maintain confidentiality of quality records and product information.
• Promote a strong quality culture across manufacturing and support departments.