Associate Director Pharmacovigilance and Quality Assurance

I am exclusively mandated by a market-leading oncology pharmaceutical multinational to appoint an Associate Director, Quality Assurance & Pharmacovigilance (QA & PV).

This is a high-impact Asia Pacific regional role based in Taiwan, supporting a leading organization with a globally recognized portfolio of commercialized, patented therapeutic antibody products in oncology, underpinned by an extensive international R&D network spanning more across 13 countries.

The position holds significant regional visibility and influence across QA and PV strategy within APAC, with a strong focus on Taiwan as the operational base.

This is an individual contributor role, working in close partnership with the on-the-ground Pharmacovigilance team in Taiwan, while driving cross-functional quality and PV initiatives across the wider Asia Pacific region.

The successful candidate will play a pivotal role in strengthening compliance frameworks, leading continuous improvement initiatives, and supporting transformational quality system enhancements across a complex, multi-market environment.

To be successful, you would bring at least 15 years experience in Quality Assurance and Pharmacovigilance within pharmaceuticals, biologics, or vaccines, along with a strong track record in organizational transformation, quality systems leadership, and change management.

Experience engaging with regional health authorities across Asia, including MFDS, Taiwan FDA, PMDA and other APAC regulatory bodies, will be highly advantageous.

For a confidential discussion about this high-impact opportunity, please click apply.

CEI: R2090154 | License No.: 22S1313