Site Quality Head Changping

Job description

Band Level 6 Job Description Summary Lead the site quality organization to ensure regulatory compliance, product quality, and operational excellence across all manufacturing activities, in alignment with cGMP, ISO standards, and Novartis quality policies. Job Description Core Responsibilities Quality Leadership & GovernanceLead and structure the site Quality organization to support all manufacturing operations Establish and maintain an effective Quality Management System (QMS) Drive quality governance, including Management Review and performance monitoring Own Manufacturing Quality Systems within the SM platform Regulatory Compliance & Inspection ReadinessEnsure full compliance across all products with regulatory and corporate quality standards Maintain continuous inspection readiness and audit compliance Manage regulatory registrations and authority interactions Lead internal/external audits and GxP inspection activities Product Quality & ReleaseEnsure quality across all manufacturing streams (solid, ophthalmic, aseptic) Approve batch release ensuring compliance with filings and specifications Approve Product Quality Reviews (PQR/APQR) Act as Qualified Person / Technical Responsible Person Quality Systems & Risk ManagementLead risk-based quality management and continuous improvement Ensure effective management of deviations, OOS/OOX, complaints, and recalls Act as escalation point for critical quality issues Monitor Key Quality Indicators (KQIs) GxP Oversight & Change ManagementProvide oversight across all GxP processes Ensure compliant and timely handling of change controls Ensure data integrity, eCompliance, and regulatory adherence Qualification, Validation & EquipmentEnsure facilities, utilities, and equipment are qualified and maintained Ensure all products undergo appropriate process validation Leadership & CultureBuild and develop high-performing Quality teams Drive talent management, succession planning, and capability building Foster a culture aligned with Novartis values: Inspired, Curious, Unbossed Ensure workforce training and GMP qualification compliance HSE & Business ContinuityPromote strong Safety & Quality culture Ensure business continuity and crisis management readiness Participate in site emergency management as required Key Accountabilities (China GMP Focus)Ensure effective operation of Quality Assurance & Quality Control systems Guarantee data integrity, traceability, and regulatory compliance Approve and oversee: Batch records and release Deviations, change controls, and investigations Validation, qualification, and technical documentation Ensure effective: Supplier qualification Stability programs Complaints and recall handling Lead periodic quality risk reviews and continuous improvement Ideal Candidate ProfileExperience12–15+ years in pharmaceutical QA/QC and/or manufacturing Strong experience in GMP, aseptic and solid dosage environments Proven leadership in operations, quality systems, and cross-functional collaboration EducationDegree in Pharmacy, Chemistry, Engineering, Biotechnology or equivalent LanguagesFluent English; local language preferred Key CompetenciesStrategic leadership & change management Deep expertise in GxP quality systems Strong stakeholder engagement and regulatory interface Risk management & decision-making capability Communication and influencing skills Skills Desired Analytical Thinking, Business Acumen, Business Strategy, Collaboration, Communication Skills, Data Integrity, Decision Making, Digital saviness, Finance Acumen, Industry standards Knowledge, Leadership, Organizational Saviness, Risk Management, Smart Risk Taking, Stakeholder Management, Storytelling, Strategic Planning, Strategic Thinking