Hiring Agm/dgm

Minimum 20 years in Quality Assurance Quality Systems in API pharmaceutical manufacturing with significant exposure to regulated markets To provide strategic and operational leadership to the Quality function ensuring robust implementation of quality systems compliance with global regulatory requirements and continuous improvement in all quality-related processes for API manufacturing Key Responsibilities Quality Systems Compliance Implement maintain and continuously improve Quality Systems in line with ICH Q7 EU GMP 21 CFR Parts 11 210 211 Annex 11 and other applicable global regulations for APIs Ensure site-wide compliance with internal quality policies SOPs and regulatory guidelines Oversee preparation revision and effective implementation of quality-related SOPs policies and quality manuals Vendor Qualification Management Establish and maintain procedures for vendor approval qualification periodic evaluation and rejection Ensure technical and quality assessment of raw material intermediate and service providers in alignment with regulatory and company standards Drive supplier quality improvement initiatives and manage critical vendor-related quality issues Change Control Deviations Risk Product Quality Review Review and approve major process changes and critical quality-impacting changes through the Change Control system Review and approve Annual Product Quality Reviews APQR PQR and ensure implementation of improvement actions Review and approve critical deviations investigations and associated Corrective and Preventive Actions CAPA Lead Quality Risk Management activities and ensure implementation of risk mitigation strategies Oversee preparation review and approval of Site Master File SMF Investigations OOS OOT Rework Repacking Ensure thorough timely and scientifically sound investigations of OOS Out of Specification OOT Out of Trend and other critical quality events Approve and oversee activities related to repacking relabeling rework and associated deviations ensuring compliance and product integrity Ensure effective root cause analysis and CAPA implementation for all critical quality issues Market Complaints CAPA Ensure robust investigation of market complaints including coordination with cross-functional teams Approve complaint investigation reports and ensure effective CAPA and follow-up to prevent recurrence Monitor complaint trends and drive continuous improvement initiatives based on trend analysis Regulatory Audits Inspections Lead preparation for coordination of and responses to regulatory inspections and customer audits USFDA TGA EU WHO ANVISA and other authorities Ensure timely closure of audit observations with effective sustainable CAPA Maintain a state of constant audit readiness across the site People Leadership Training Lead mentor and develop the Quality Assurance and related quality teams to build strong technical and compliance capabilities Plan and implement training programs on GMP data integrity quality systems and regulatory updates for all relevant personnel Foster a culture of quality transparency and continuous improvement across the organization Qualifications M Pharm B Pharm M Sc Chemistry or higher degree in a relevant scientific discipline Minimum 20 years of experience in Quality Assurance Quality Systems in API pharmaceutical manufacturing with at least 5-8 years in a senior leadership role Strong knowledge of ICH Q7 EU GMP 21 CFR Parts 11 210 211 Annex 11 and other global GMP requirements applicable to APIs Proven experience in handling multiple regulatory inspections e g USFDA TGA EU WHO ANVISA etc Key Competencies Strong leadership team management and decision-making skills Deep understanding of GMP quality systems and regulatory expectations for APIs Excellent analytical investigation and problem-solving skills RCA risk assessment CAPA Strong communication stakeholder management and audit-facing skills High integrity and strong focus on data integrity and compliance