Regional Regulatory Affairs Specialist – Dossiers & Licenses

GMP Group; Singapore; On-site; SGD 40,000 - 55,000; Full time

Job summary

A leading pharmaceutical company in Singapore is seeking a Regulatory Affairs professional to manage regulatory documentation, ensure license maintenance, and support the regulatory team. Candidates should have a Bachelor's degree in Pharmacy or Life Sciences and ideally possess 1-2 years of relevant experience. The role offers the opportunity to contribute to significant projects within the healthcare sector and requires a commitment starting 1 Dec 2025.

Qualifications

• 1-2 years of Regulatory Affairs experience in pharmaceuticals or consumer health.
• Knowledge in dossier preparation, artwork management, and regulatory databases.
• Strong attention to detail and organizational skills.

Responsibilities

• Manage preparation of regulatory documents for OHC projects.
• Support RA team to manage artworks and maintain Veeva database.
• Ensure required licenses are maintained and renewed on time.

Skills

Regulatory Affairs experience

Attention to detail

Organizational skills

Education

Bachelor's degree in Pharmacy, Life Sciences, or related field

Job description

A leading pharmaceutical company in Singapore is seeking a Regulatory Affairs professional to manage regulatory documentation, ensure license maintenance, and support the regulatory team. Candidates should have a Bachelor's degree in Pharmacy or Life Sciences and ideally possess 1-2 years of relevant experience. The role offers the opportunity to contribute to significant projects within the healthcare sector and requires a commitment starting 1 Dec 2025.