Charles Conrad Rambung

Orchestrated the complete lifecycle of health research projects, from conceptualization and budget planning to execution and final high-quality report generation, consistently meeting deadlines.

Developed and published impactful research reports, contributing to the understanding and addressing of critical public health issues in East Nusa Tenggara.

Cultivated and maintained robust partnerships with academic institutions, research fellows, and key stakeholders, enhancing collaborative research efforts and dissemination.

Ensured research findings were effectively communicated and understood by diverse audiences, translating complex data into actionable insights for government and public benefit.

Successfully achieved research objectives, contributing to a positive public perception of government health initiatives and driving policy recommendations.

Managed and executed comprehensive health research projects, including design, budget allocation, and timeline adherence, culminating in high-quality reports and publications.

Produced and disseminated research findings to various stakeholders, ensuring clarity and understanding to inform public health strategies and interventions.

Forged and sustained effective communication channels and working relationships with academic partners, research fellows, and government entities, facilitating collaborative research.

Translated complex research objectives into tangible outcomes, contributing to an enhanced public image for government-led health initiatives.

Ensured all research findings were understood and utilized by stakeholders, driving informed decision-making and contributing to public health improvements.

Ensured the safe, appropriate, and economical use of medications across the hospital, impacting patient care for hundreds of daily cases.

Provided critical pharmacological information to physicians and medical staff, clarifying drug dosages, side effects, and interactions to prevent adverse events.

Contributed significantly to clinical pharmacy activities, enhancing patient safety and medication efficacy through expert consultation and therapeutic monitoring.

Counseled patients on drug therapies, improving medication adherence and understanding, leading to better health outcomes.

Prepared and reviewed medications, meticulously interpreting physician orders and detecting therapeutic incompatibilities to maintain high standards of patient safety.

Developed over 10 robust, stable, and effective solid and liquid oral formulations, successfully transitioning them for in-house and 3rd party manufacturing.

Conducted comprehensive raw material research and compiled documentation for pre-formulation assessments, ensuring 100% compliance with testing specifications and regulatory requirements.

Authored detailed manufacturing trial documentation for pilot and small production runs, facilitating smooth scale-up operations.

Collaborated with production technicians in setting up and operating pilot-scale equipment, successfully completing small production runs and validating manufacturing processes.

Streamlined material sourcing and assessment processes for new and existing products, improving efficiency and compliance for the R&D department.

Designed and implemented new Standard Operating Procedures (SOPs) for the QC Laboratory, enhancing operational efficiency and compliance.

Performed final quality checks on all products, ensuring adherence to stringent quality assurance standards prior to release.

Ensured 100% compliance of quality control measures with company and industry regulatory requirements, maintaining product integrity and safety.

Implemented and maintained all relevant procedures within the company's quality management system, contributing to enhanced product quality.

Managed the update, revision, and modification of in-house systems and procedures to meet evolving certification body requirements, ensuring continuous compliance.