Following a year of success, an Asian Pharma company is looking to start their second phase of growth after entering Singapore just last year. They are currently looking for a Regulatory Affairs Manager to drive registration approvals across SEA for their products.
The work has already started, and they have a long list of products that they wish to get approved, this role will report directly into the Singapore GM offering advice and insights on the SEA regulatory landscape.
As the Regulatory Affairs Manager you will lead all things RA, you will have market & business level influence and responsibility and will be considered a key opinion leader and an expert resource within the SEA business.
The RA Manager will be responsible for:
- Oversee the registration of company products in Singapore and Southeast Asia, identifying risks in registration phases and advancing projects per company goals.
- Coordinate with internal teams and external partners for project planning and management; compile and submit regulatory documents as per Southeast Asian requirements.
- Track document review, address issues promptly, maintain communication with regulatory bodies, and assist in on-site GMP audits as required by regional agencies.
The RA Manager will be / have:
- RA experience in pharma industry
- Regional RA experience preferred
- Degree qualified
- Fluency in Chinese for internal & external communications and engagement
If you feel you would be suitable then please get in touch for a further conversation.
Reg No. R1871342
BeathChapman Pte Ltd
Licence no. 16S8112
