Quality Assurance Executive

1. QA Executive – Junior Level

Experience Required:

Salary Offered:

Job Summary:

We are seeking motivated QA Executives with 2–4 years of experience to support daily quality assurance activities in a GMP-regulated pharmaceutical facility. The role will focus on documentation review, QA activities, and ensuring compliance with regulatory standards.

Key Responsibilities:

• Review batch manufacturing and packing records
• Line clearance for production and packaging activities
• Support in handling deviations, change controls, CAPA, and incident reports
• Ensure compliance with cGMP and Revised Schedule M requirements
• Participate in in-process checks and quality monitoring
• Assist in preparation and review of SOPs, logbooks, and other controlled documents
• Support internal audits and regulatory inspection readiness

Qualifications:

• B.Pharm / M.Pharm / B.Sc / M.Sc (Life Sciences/Chemistry)
• 2–4 years of experience in QA in a pharmaceutical company
• Good understanding of cGMP and QMS principles
• Strong documentation and communication skills

2. QA Executive – Mid-Level

Experience Required:

Salary Offered:

Job Summary:

We are looking for experienced QA Executives with 4–8 years of experience to take responsibility for advanced QA functions, including compliance management, documentation oversight, and training of junior QA staff.

Key Responsibilities:

• Review and approval of batch records, logbooks, and controlled documents
• Oversee line clearance, in-process checks, and QA compliance
• Lead and investigate deviations, OOS, OOT, change controls, and CAPA
• Coordinate with production, QC, and engineering for quality compliance
• Handle document control, issuance, archival, and retrieval systems
• Support vendor qualification and raw material quality compliance
• Prepare for and participate in internal audits and regulatory inspections
• Mentor and guide junior QA team members

Qualifications:

• B.Pharm / M.Pharm / B.Sc / M.Sc (Life Sciences/Chemistry)
• 4–8 years of QA experience in a pharmaceutical manufacturing unit
• Strong knowledge of QMS, regulatory compliance, and cGMP
• Experience in facing audits (USFDA/WHO/other regulatory bodies is an advantage)
• Excellent analytical, communication, and leadership skills