QA Manager

Sujata Nutri Pharma; Vadodara; On-site; INR 600,000 - 800,000; Full time

Job summary

Sujata Nutri Pharma in Vadodara is seeking a proactive QA Manager to oversee Quality Assurance activities, ensuring compliance with regulatory requirements and Good Manufacturing Practices (GMP). The ideal candidate will have 2–3 years of experience in the pharmaceutical or chemical industry, along with strong knowledge of quality systems.

Key responsibilities include managing the Quality Management System, reviewing quality records, and conducting internal audits. The role demands adherence to Good Documentation Practices and effective communication across various departments.

Qualifications

• Strong knowledge of Quality Assurance systems and regulatory compliance.
• Experience in handling deviations, CAPA, change control, and audit management.
• Good understanding of GMP, GLP, GDP, and documentation practices.

Responsibilities

• Manage and maintain the Quality Management System (QMS).
• Review and approve SOPs, specifications, protocols, reports, and quality records.
• Conduct internal audits and support customer, vendor, and regulatory audits.

Skills

Quality Assurance systems knowledge

Regulatory compliance expertise

Experience with CAPA

Knowledge of GMP

Proficiency in MS Office

Job description

Job Summary

We are looking for a proactive and quality-focused QA Manager to oversee Quality Assurance activities and ensure compliance with quality systems, regulatory requirements, and Good Manufacturing Practices (GMP). The ideal candidate will have 2–3 years of experience in Quality Assurance within the pharmaceutical, chemical, or related manufacturing industry.

Key Responsibilities

• Manage and maintain the Quality Management System (QMS).
• Review and approve SOPs, specifications, protocols, reports, and quality records.
• Handle deviations, CAPA, change controls, OOS investigations, and risk assessments.
• Ensure compliance with GMP, GLP, GDP, SOPs, and regulatory requirements.
• Conduct internal audits and support customer, vendor, and regulatory audits.
• Investigate deviations, non-conformances, OOS, and customer complaints.
• Prepare and maintain QA/QC documentation, reports, and records.
• Support internal audits, vendor audits, and regulatory inspections.
• Coordinate with Production, QC, Warehouse, and other departments on quality-related matters.
• Ensure adherence to Good Documentation Practices (GDP).
• Lead quality improvement initiatives and ensure continuous compliance.

Qualifications

• Strong knowledge of Quality Assurance systems and regulatory compliance.
• Experience in handling deviations, CAPA, change control, and audit management.
• Good understanding of GMP, GLP, GDP, and documentation practices.
• Knowledge of pharmaceutical or chemical manufacturing processes.
• Experience in quality documentation review and approval.
• Proficiency in MS Office and quality management tools.

Experience

2–3 Years of relevant experience.

Working Hours

10:00 AM - 06:30 PM.