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Pharmaceutical Science Intern

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Onsite

Pharmaceutical Science Intern

Miraco Nutripharm Pte Ltd

Pharmaceutical Science Intern

Skills

Testing & QABusiness DevelopmentCompliance

2 months ago

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Important information


Contract type:

Permanent

Location:

Singapore

Work mode:

Onsite

Published on:

9 August 2026

What they need


Company

Miraco Nutripharm

miraconutripharm.com

Designation

Pharmaceutical Science Intern

Date Listed

10 Jun 2026

Job Type

Entry Level / Junior Executive

Intern/TS

Job Period

From 01 Jul 2026 - 31 Dec 2026

Profession

Healthcare / Pharmaceutical / Sports

Industry

Healthcare / Fitness / Sports

Location Name

Singapore

Allowance / Remuneration

$800 - 1,000 monthly

Company Profile

At Miraco Nutripharm, we are dedicated to advancing health & improving lives. Our goal is to relieve 1 billion people worldwide of pain & discomfort. If you know of anyone who has been worried about or suffered from any health problems, join us in making a positive impact by reducing the pain & distress others have to endure.

Job Description

As a Pharmacy Intern, you will work closely with the Regulatory and Business Development team to ensure our pharmaceutical drugs and health supplements meet local regulatory standards and are supported by strong scientific evidence.

Key Responsibilities:

  1. Regulatory Intelligence & Compliance
  • HSA Registry Management: Conduct systematic research using the HSA Infosearch and other public registries to verify product registrations and ensure internal databases are aligned with the latest local classifications.
  • Regulatory Horizon Scanning: Monitor and report on updates to the Medicines Act and Singapore Food Regulations to ensure health claims for supplements (e.g., probiotics, joint health) remain compliant with evolving local standards.
  1. Medical Affairs & Evidence-Based Support
  • Literature Synthesis & Appraisal: Critically review and summarize Randomized Controlled Trials (RCTs) and peer-reviewed journals to provide evidence-based justifications for product efficacy in various therapeutic areas.
  • Scientific FAQ Development: Assist in drafting technical response scripts and FAQs for the sales team to address clinical queries from General Practitioners (GPs) and Specialists regarding mechanism of action or ingredient stability.
  • CME Coordination: Support the preparation and coordination of Continuing Medical Education (CME) materials, ensuring all clinical content aligns strictly with approved product indications and local medical codes of conduct.
  1. Digital Learning & Training Excellence
  • Learning Management System Content Curation: Support the end-to-end update and maintenance of clinical training modules and product information on Google Classroom, ensuring all digital assets are current and accurate.
  • Knowledge Base Development: Source and categorize approved and publicly available content to build a comprehensive internal reference library for the medical and marketing teams.
  1. Market Analysis & Operations
  • Competitor Benchmarking: Perform technical "deep-dives" into competitor formulations, comparing active ingredient concentrations, dosage forms, and specialty usage to support internal portfolio benchmarking.
  • Quality Assurance (GDP) Support: Apply Good Distribution Practice (GDP) principles to assist in the oversight of cold-chain logs and storage conditions for temperature-sensitive pharmaceuticals and supplements.
  • Post-Market Surveillance: Support the Pharmacovigilance (PV) workflow by documenting and categorizing product feedback or adverse event reports from healthcare professionals

Application Instructions

Please apply for this position by submitting your CV to [email protected]

Apply for this position

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