Detail-oriented Pharmaceutical Technology graduate with hands-on experience in research and development, quality control, and regulatory documentation. Skilled in technical writing, data analysis, formulation support, and compliance with pharmacopeial standards (BP, USP, EP). Experienced in preparing reports, stability documentation, ingredient justification, and laboratory records with strong accuracy and organization. Adept at supporting projects independently and collaboratively, delivering structured, reliable, and deadline-driven work for scientific, regulatory, and documentation-based freelance projects.
We will review the reports from both freelancer and employer to give the best decision. It will take 3-5 business days for reviewing after receiving two reports.