Regulatory Affairs Specialist

Reeracoen Singapore Pte Ltd; Singapore; Hybrid; SGD 50,000 - 70,000; Full time

Job summary

A leading pharmaceutical company in Singapore is seeking a Regulatory Affairs Specialist. The ideal candidate will have at least 2 years of experience in the regulatory field, particularly within the pharmaceutical industry in Singapore. Responsibilities include coordinating regulatory submissions and developing strategies across the ASEAN region. Benefits include annual leave, medical benefits, and flexible working arrangements.

Benefits

AWS

Variable Bonus

Annual Leave 14 days

Medical Benefits

Flexible Benefits (S$1500/year)

Work from Home once a week

Qualifications

• Minimum 2 years of experience in Regulatory Affairs within Singapore's pharmaceutical industry.
• Ability to adapt to changes and work under pressure.

Responsibilities

• Handle mainly regulatory operations tasks
• Coordinate regulatory submissions (new and variation) across Asia/ASEAN
• Develop regulatory strategies with cross-functional teams

Skills

Proficiency in written and spoken English

Strong communication and negotiation skills

Proactive and self-motivated

Education

Diploma in any discipline

Job description

Overview

Job title: Regulatory Affairs Specialist. Reference ID: 36639. Our client, a Japanese pharmaceutical company, is currently seeking to hire a Regulatory Affairs Specialist to support operations across Asia and the ASEAN region. The primary responsibilities of this role include coordinating regulatory submissions, supporting strategy development, and monitoring activities across local affiliates. You will be reporting to the Regulatory Affairs Department in Japan.

Responsibilities

• Handle mainly regulatory operations tasks
• Report directly to the Regulatory Affairs Department in Japan
• Coordinate regulatory submissions (new and variation) across Asia/ASEAN
• Manage regulatory documents and ensure timely submissions
• Develop regulatory strategies with cross-functional teams
• Track and monitor local affiliate regulatory activities
• Identify and resolve regulatory issues proactively

What you will receive

• AWS
• Variable Bonus (Depends on Company and Individual performance)
• Annual Leave 14 days
• Medical Leave
• Medical Benefits
• Flexible Benefits (S$1500/year)
• WFH: Once a week to be at Office, others day WFH

Requirements & Preferences

(Must)

• Diploma in any discipline.
• Minimum 2 years of experience in Regulatory Affairs within Singapore's pharmaceutical industry.
• Proficiency in both written and spoken English is required to liaise with counterparts and handle documentation.
• Proactive, self-motivated, and able to take initiative with high energy levels.

(Advantageous)

• Strong communication and negotiation skills.
• Logical thinking and sound problem-solving capabilities.
• Ability to adapt well to changes and work effectively under pressure.
• Possess regional experience in a large pharmaceutical company is an advantage.

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We regret that only shortlisted candidates will be notified.

Registration No.: R1217125 (Yeo Ker Ling Caroline)
Recruitment Licence: 12C5051