Job Description

• Participated in importexport inspection, product seizure investigations, and document verification at regulatory checkpoints. Assisted in pre-import authorization and enforcement of health product regulations. Collected and analyzed laboratory testing results and inspection findings to assess product compliance and safety. Evaluated non-compliant imported products and recommended regulatory actions, including product recall, seizure, destruction, or release from detention. Studied international regulations and standards, coordinated data exchange, and contributed to risk communication and early warning systems to support safe international trade of health products. Supported the development and maintenance of online systems for submission, tracking, and release of products at FDA checkpoints. Coordinated policy implementation, monitored outcomes, and contributed to operational, budget, and personnel development planning. Provided guidance to importers and exporters on regulatory requirements and procedures. Assisted in drafting project proposals related to capacity building in health product diagnostics.

Job Description

• - Supported registration of modern medicines and generic drugs in Thailand.
• - Assisted in drug variation submissions in compliance with ASEAN Variation Guidelines.
• - Prepared and reviewed regulatory documents (SmPC, PIL) according to ASEAN labeling requirements.
• - Practiced Docubridge submission, document upload, and tracking processes.
• - Reviewed Thai FDA regulations, notifications, and SOPs related to drug registration, variation, advertisement approval, and license renewal.
• - Conducted regulatory research for international drug registration requirements.

Job Description

• REGULATORY AFFAIRS, QUALITY ASSURANCE & SALES/MARKETING INTERN
• - Learned regulatory strategies for drug, vaccine, and biologics registration.
• - Studied laws and regulations related to drug registration, variation, advertisement, and FDA reporting.
• - Gained QA experience in product recall, complaint handling, lot release, supplier qualification, and regulatory documentation verification.
• - Gained comprehensive knowledge in pharmacovigilance, including ADR reporting, ICSR submission, and signal detection.
• - Prepared regulatory and legal documents for pharmaceutical products in compliance with drug regulations to support sales teams in presenting and distributing
• product information to healthcare professionals in hospitals.
• SALES & MARKETING EXPOSURE
• - Learned product positioning, promotional planning, and go-to-market strategies for pharmaceutical products.
• - Understood alignment between regulatory requirements and marketing strategy.
• - Developed insight into how to effectively communicate product value to healthcare professionals.

Job Description

• Pharmaceutical Manufacturing Intern
• - Reviewed protocols and supported equipment qualification (IQ, OQ, PQ).
• - Analyzed plant layout and production flow to ensure GMP compliance.
• Quality Management (QA/QC) Intern
• Pharmaceutical Manufacturing Intern
• - Reviewed protocols and supported equipment qualification (IQ, OQ, PQ).
• - Analyzed plant layout and production flow to ensure GMP compliance.
• Quality Management (QA/QC) Intern
• - Performed analytical testing of raw materials and finished products.
• - Conducted stability studies and shelf-life evaluation.
• - Participated in Analytical Method Validation processes.

Job Description

• - Designed and developed training programs for personnel in herbal product manufacturing.
• - Created and evaluated assessment tests based on GMP (modern and traditional medicines) in compliance with Thai drug regulations (B. E. 2567).
• - Gained hands-on understanding of herbal product manufacturing processes and production workflows. Strengthened ability to translate regulatory requirements into practical training and communication.

Job Description

• - Reviewed and evaluated drug registration dossiers, ensuring compliance with Thai FDA and ASEAN guidelines.
• - Interpreted scientific and clinical data to support regulatory decision-making.
• - Collaborated with internal teams to streamline document screening processes.
• Developed strong attention to detail and ability to communicate regulatory concepts clearly.