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The regulatory assistant will support Nyprax Pharma, a regulatory affairs consultancy with over 20 years of experience, in managing medical device regulatory submissions in Singapore. Responsibilities include coordinating and submitting documentation to the Health Sciences Authority, preparing medical device dossiers, verifying report accuracy, and addressing queries from regulatory authorities. The role requires strong organizational skills and attention to detail. The position offers a salary of 3,000.
This summary is AI-generated and may contain inaccuracies. Please refer to the full job description below.
[This job id 16028 first appeared in Job-Q.com on 22 Jun 2026]
Company Overview
Nyprax Pharma is a growing Regulatory Affairs Consultancy with 20+ years of experience. We provide expert guidance to ensure smooth regulatory submissions for medical devices to be imported, distributed, and marketed in Singapore.
Job Summary
You will coordinate and submit regulatory documentation to the Health Sciences Authority, compile and format medical device dossiers, verify report accuracy, and respond to Ministry queries while managing multiple tasks under deadlines.
Responsibilities
Required competencies and certifications
Preferred competencies and qualifications
Other Information
Benefits
Contact Bharat Kumar (bharat@nyprax.com)
Company Website www.nypraxpharma.com
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