This is a senior regional role for a hands-on QA professional with deep expertise in GxP, Medical Affairs, and risk-based quality management, operating within a complex global matrix environment.
Key focus areas:
- QA leadership across Clinical Development, Medical Affairs, PV and Quality
- Direct engagement with global ®gional Health Authorities
- Leading complex global projects in a matrix environment
This role offers strong regional visibility, inspection exposure, and the opportunity to shape Medical QA strategy across Asia.
The successful candidate will come with:
- Bachelor’s degree in Life Sciences, Healthcare, or related discipline (Master’s preferred) with 10+ years of experience in regulated pharmaceutical environments spanning Medical Affairs, Clinical Development, and/or Quality Assurance(preferred)
- Strong knowledge of global regulatory expectations and inspection processes
- Proven leadership experience managing regulated activities across Clinical Development, Medical Affairs, Pharmacovigilance and/or Quality Assurance, with a strong track record of working cross-functionally in a global, matrix pharmaceutical environment.
- Hands-on experience engaging directly with Global, Regional, and Local Health Authorities(e.g. FDA, EMA, MHRA, HSA, NPRA, MFDS, TFDA, etc.), with a strong understanding of clinical development requirements and the science of product development.
- Demonstrated experience leading and managing global projects, influencing senior stakeholders and driving outcomes across regions.
Qualified candidates are encouraged to apply or reach out confidentially for further discussion.
Reg. No. R1110770
BeathChapman Pte Ltd
Licence no. 16S8112
