Quality Assurance Manager

Drlogy; Nangal Baola; On-site; INR 1,200,000 - 1,600,000; Full time

Job summary

Drlogy seeks a Quality Assurance Manager in Nangal Baola, Rajasthan to oversee pharmaceutical quality assurance systems. This role requires strong expertise in AQA, audits, and compliance with regulatory standards. Candidates should possess B.Pharm or M.Pharm qualifications and 12 to 15 years of experience in quality assurance, ensuring adherence to GMP and managing documentation and audits effectively.

The ideal applicant will lead audits, review quality documents, and support regulatory audit readiness while fostering a culture of compliance and continuous improvement within the team.

Qualifications

• 12 to 15 years of experience in quality assurance.
• Strong knowledge of AQA, audits, compliance systems, and regulatory expectations.

Responsibilities

• Manage quality assurance systems across pharmaceutical operations.
• Ensure compliance with GMP, regulatory standards, and company SOPs.
• Lead audits, inspections, and quality system implementation.
• Review and approve quality documents, batch records, and SOPs.
• Manage QMS activities including deviations and CAPA.
• Support regulatory audits and customer audit readiness.

Skills

AQA

Quality Assurance

Pharma QA

QMS

Audit

GMP Compliance

Education

B.Pharm or M.Pharm qualification

Job description

Work Mode

Work From Office

Department

Quality Assurance

Employment type

• Full time

Key Skills

AQA

Quality Assurance

Pharma QA

QMS

Audit

GMP Compliance

Preference Languages

Any Language

Job Description

Quality Assurance Manager is responsible for managing pharma QA systems, audits, QMS, GMP compliance, documentation, and assurance activities across manufacturing operations. The requires B.Pharm or M.Pharm qualification with 12 to 15 years of experience in quality assurance. Candidates should have strong knowledge of AQA, audits, compliance systems, regulatory expectations, and pharmaceutical quality management.

Role & Responsibilities

• Manage quality assurance systems across pharmaceutical operations.
• Ensure compliance with GMP, regulatory standards, and company SOPs.
• Lead audits, inspections, and quality system implementation.
• Review and approve quality documents, batch records, and SOPs.
• Manage QMS activities including deviations, CAPA, change control, and complaints.
• Coordinate with production, QC, warehouse, and engineering departments.
• Monitor compliance status of manufacturing and documentation practices.
• Support regulatory audits and customer audit readiness.
• Guide QA team members in documentation and compliance activities.
• Review validation, qualification, and process compliance documents.
• Ensure timely closure of quality events and corrective actions.
• Conduct training on GMP, documentation, and quality systems.
• Identify quality risks and implement preventive measures.
• Prepare quality reports for management review.
• Maintain a strong culture of compliance and continuous improvement.