Regulatory Affairs Specialist (Worked in HSA or experienced in RA)

ALCOTECH PTE. LTD.; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A specialist regulatory company in Singapore is looking for a Regulatory Affairs Specialist. The role includes preparing medical device registration dossiers for HSA and ensuring compliance with regulations. Ideal candidates have 2–5 years of regulatory affairs experience and strong knowledge of Singapore's medical device regulations. The job offers a salary range of $4,100 to $5,300 monthly and opportunities for professional growth.

Benefits

Career growth opportunities

Professional development

Qualifications

• Minimum 2–5 years of regulatory affairs experience.
• Strong knowledge of regulations from Health Sciences Authority (HSA).
• Experience with Therapeutic Products License (TPL) is preferred.

Responsibilities

• Prepare and submit medical device registration dossiers to HSA.
• Advise on regulatory strategy and compliance requirements.
• Monitor regulatory changes and ensure compliance.

Skills

Regulatory affairs experience

Knowledge of Singapore medical device regulations

Bilingual in English and Chinese

Organizational skills

Project management skills

Job description

Alcotech Pte Ltd specializes in Infectious Disease Kits and Medical Device Regulatory Affairs. We support medical device manufacturers in navigating complex regulatory landscapes and securing market access across Singapore and Southeast Asia.

Role Overview

We are seeking a Regulatory Affairs Specialist with either experience working at the Health Sciences Authority (HSA) or prior experience in medical device regulatory affairs. The ideal candidate will manage medical device registrations, ensure compliance with regulations, and provide guidance on regulatory strategy.

Key Responsibilities

• Prepare, review, and submit medical device registration dossiers to HSA. Monitor submissions in other ASEAN countries handled by local regulatory personnel.
• Advise on regulatory strategy, product classification, labelling, and compliance requirements.
• Monitor regulatory changes and provide guidance to ensure ongoing compliance in Singapore and ASEAN markets.
• Support post-market surveillance activities.
• Point of contact for manufacturers\' regulatory team and regulatory authorities, ensuring smooth and timely registration processes.

Requirements

• Minimum 2–5 years of regulatory affairs experience, either from prior work in HSA or a regulatory affairs role in medical devices.
• Strong knowledge of Singapore medical device regulations (HSA); familiarity with other ASEAN regulations is an advantage.
• Ability in speaking both English and Chinese is a requirement. We have clients all over the world.
• Strong organizational and project management skills; able to handle multiple submissions simultaneously.
• Familiarity with Therapeutic Products License (TPL) is preferred.

Work Environment

• Office-based role
• Monday – Friday, 9:00 am – 6:00 pm
• Location: 25 Bukit Batok Crescent, #09-13 The Elitist, Singapore 658066

Salary

$4,100 – $5,300 monthly, based on experience

Why Join Us

• Leverage your HSA or regulatory affairs experience to lead submissions across multiple medical device product lines.
• Work closely with clients and regulatory authorities in a high-impact role.
• Gain exposure to ASEAN regulatory environments while building professional expertise.
• Join a specialist regulatory company offering career growth and professional development opportunities.