[Pharmaceutical – RA Manager – Singapore – Full-time – Permanent]
I am representing a prominent pharmaceutical company in their search for a new RA Manager.
This leading organization specializes in the manufacturing and distribution of CNS and Ophthalmology therapies.
In this newly created role, you will join a well-established Regulatory Affairs team and take on a highly strategic individual contributor position.
Your responsibilities will include overseeing regulatory compliance and implementing strategic submission plans.
The company is renowned for its long-term vision and growth, offering significant career advancement opportunities.
As the RA Manager, you will have the unique chance to drive innovation and be a catalyst for change across the Asia-Pacific region.
Key qualifications for the RA Manager role include:
• Experience with regulatory submissions for the Singapore, Malaysia, Brunei cluster, as well as China, Korea, and Taiwan.
• A minimum of 5 years of experience in Regulatory Affairs.
• Expertise in the submission of pharmaceutical products.
• Knowledge of clinical development processes.
Office No.: +65 6964 0700 | CEI: R2090154 | Licence No.: 22S1313
[Pharmaceutical – RA Manager – Singapore – Full-time – Permanent]
I am representing a prominent pharmaceutical company in their search for a new RA Manager.
This leading organization specializes in the manufacturing and distribution of CNS and Ophthalmology therapies.
In this newly created role, you will join a well-established Regulatory Affairs team and take on a highly strategic individual contributor position.
Your responsibilities will include overseeing regulatory compliance and implementing strategic submission plans.
The company is renowned for its long-term vision and growth, offering significant career advancement opportunities.
As the RA Manager, you will have the unique chance to drive innovation and be a catalyst for change across the Asia-Pacific region.
Key qualifications for the RA Manager role include:
• Experience with regulatory submissions for the Singapore, Malaysia, Brunei cluster, as well as China, Korea, and Taiwan.
• A minimum of 5 years of experience in Regulatory Affairs.
• Expertise in the submission of pharmaceutical products.
• Knowledge of clinical development processes.
Office No.: +65 6964 0700 | CEI: R2090154 | Licence No.: 22S1313