- Directs all plant-level Quality Assurance (QA) and Quality Control (QC) operations. This strategic leadership role ensures that pharmaceutical products are manufactured, tested, and released in strict compliance with cGMP, FDA, EMA, and PIC/S regulatory standards
- QMS Management: Establish, optimize, and maintain the Quality Management System (QMS) to ensure 100% regulatory compliance.
- Compliance & Audits: Oversee customer audits, regulatory inspections, deviation investigations, and Corrective and Preventive Actions (CAPA).
- Batch Release: Review and approve validation master plans, batch records, and product specifications to guarantee safety and product efficacy.
- Team Leadership: Manage, train, and evaluate the performance of site QA/QC teams, fostering a robust quality culture across the facility.
- Stakeholder Alignment: Represent the Quality function in cross-functional project teams and ensure customer quality agreements are met
- Bachelor's Degree in Pharmacy, Chemistry, Life Sciences, or Chemical Engineering
- 10+ years of pharmaceutical quality assurance management, with at least 5 years in a supervisory or leadership role.
- Deep, hands-on knowledge of GMP manufacturing, ICH guidelines, data integrity protocols, and health authority regulations
Veronica Neo Shen Hwa - [Confidential Information]
Personnel Reg No: R1110855
Manpower Staffing Services (S) Pte Ltd
EA Licence No: 02C3423
