Miraco Nutripharm – Pharmaceutical Science Intern

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.

2. 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.

3. 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.

4. 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