Regional Regulatory Strategy Lead

MSD; Singapore; On-site; SGD 180,000 - 240,000; Full time

Job summary

Merck & Co., Inc. in Singapore seeks a Regulatory Affairs Liaison (Associate Director) to lead region-wide regulatory strategy across clinical, CMC and risk management, serving as single point of contact for products with HQ and country teams.

The role requires more than 10 years in Regulatory Affairs, an advanced science degree, and proven ability to manage regulatory submissions, HA responses, and cross-functional collaboration in a fast-paced environment.

Qualifications

• Bachelor degree in a scientific discipline with 10+ years in Regulatory Affairs.
• Strong written and verbal communication skills in a global team environment.
• Experience with regulatory requirements & HA submissions in Asia Pacific is preferred.

Responsibilities

• Owns and leads regional regulatory strategy to support product development and lifecycle management.
• Manages HA responses to Questions and coordinates regional regulatory activities with HQ and country teams.
• Ensures timely alignment of regulatory priorities across the product portfolio.

Skills

Regulatory Affairs

Clinical Research

Regulatory submissions

Education

Bachelor's degree in Pharmacy/Biology/Chemistry

Job description

Merck & Co., Inc. in Singapore seeks a Regulatory Affairs Liaison (Associate Director) to lead region-wide regulatory strategy across clinical, CMC and risk management, serving as single point of contact for products with HQ and country teams.

The role requires more than 10 years in Regulatory Affairs, an advanced science degree, and proven ability to manage regulatory submissions, HA responses, and cross-functional collaboration in a fast-paced environment.