We are seeking a highly motivated and detail-oriented QA Executive to join our team. The ideal candidate will have a strong background in the pharmaceutical, API, or chemical industry with hands-on experience in quality assurance activities. This position requires a keen eye for detail, the ability to work efficiently under pressure, and a commitment to maintaining the highest standards of quality.Key Responsibilities:Document Management: Manage and control the issuance and reconciliation of essential quality documents including BMR, ECR, BPR, SOPs, Logbooks, and Labels. Quality Systems: Perform tasks related to VQ (Validation Qualification), change control, deviation management, market complaints, and DMF readiness. Audit Readiness: Ensure that all documentation and processes are in place for successful audit outcomes and maintain compliance with regulatory requirements. Process Validation: Work closely with the process validation team to ensure that all processes meet required specifications. GMP Compliance: Maintain and ensure daily GMP (Good Manufacturing Practices) formats are followed across operations. Team Collaboration: Collaborate with other departments to support continuous improvement initiatives and maintain the quality of products in production. Required Qualifications & Skills:Education: BSc/MSc/B Pharm/M Pharm (Chemistry/Microbiology/Any other related field). Experience: Minimum of 2-3 years of experience in the pharmaceutical API, intermediate, or chemical industry. Skills: In-depth knowledge of document issuance and control (BMR, ECR, BPR, SOPs). Hands-on experience in VQ, change control, deviation management, and market complaint handling. Experience with audit readiness and process validation. Strong understanding of GMP compliance and daily GMP formats. Excellent teamwork and collaboration skills.