Site Quality Head (DGM/GM)- API Site

Key Responsibilities:

• Lead and oversee Quality Assurance (QA) and Quality Control (QC) functions at the API manufacturing facility.
• Ensure compliance with cGMP, ICH, WHO, USFDA, and other international regulatory standards.
• Manage Quality Systems — change control, deviation, CAPA, OOS/OOT, investigations, and document control.
• Review and approve SOPs, specifications, validation protocols, and batch manufacturing records.
• Coordinate internal audits, vendor audits, and regulatory inspections; ensure timely closure of audit observations.
• Oversee product release and ensure all quality parameters meet regulatory and customer requirements.
• Drive continuous improvement initiatives in quality systems and manufacturing processes.
• Train and mentor QA/QC teams to enhance compliance culture across the organization.
• Liaise with regulatory authorities and external clients for audits, product reviews, and documentation.

Ideal Candidate Profile:

• 15+ years of experience in pharmaceutical quality functions with hands on QA and QC Heading in API site
• Strong knowledge of API manufacturing and regulatory requirements
• Proven leadership and team management skills
• Passion for excellence and patient-centric outcomes