Strategic Quality Planning Contribute and execute on the long-term quality vision, aligning with company goals, and establishing key performance indicators (KPIs) to measure quality performance.
Be accountable for the achievement of the Sales budget and all Objectives set for the year. Perform actions throughout the year to ensure the achievement of results in terms of sales and other defined KPIs.
Formulate and implement a forward-looking APAC strategy for customer experience and quality that aligns with both regional nuances and worldwide corporate objectives.
The Senior Manager, Quality Operations is responsible for providing strategic leadership and oversight of Quality Operations supporting Drug Substance (DS) and Drug Product (DP) manufacturing. This includes oversight of batch disposition, material release, deviations, investigations, CAPAs, change controls, Quality Risk Assessments, New Product Introduction (NPI), and GMP manufacturing support across routine and shift operations. The role ensures adequate quality resources, effective escalation processes, and continuous quality oversight are in place to support manufacturing activities while maintaining compliance with FDA, EU GMP, PIC/S GMP, ICH guidelines, and company quality standards.
Lead and manage end-to-end integration projects for new data centre capacity, ensuring projects are completed on time, within budget, and to the required quality standards.
Design and execute structured test cases covering accuracy, tone, safety, and data privacy. This includes simulating edge cases, harmful queries, and abuse attempts.
Overall department leadership in QAQC matters with keen oversight and supervision of project deliverables to meet various Clients' and authorities' quality requirements.
Define and own the Master Test Plan and Test Strategy for assigned banking portfolios, covering System Integration Testing (SIT), User Acceptance Testing (UAT), and End-to-End (E2E) testing.
Develop, update, and implement project QA/QC plans, inspection checklists, quality procedures, and work instructions in line with ISO 9001, project specs, and industry standards.
The Director, QRM, Global QMS, R&D & PV QA is accountable for establishing, governing, and continuous advancing a robust, science- and risk-based Quality Risk Management framework across R&D & Clinical Safety Pharmacovigilance, Medical Affairs and associated quality system.
5+ years in a QA, editorial, or production role reviewing business documents, spreadsheets, and slide decks for accuracy, formatting, and consistency before external delivery