Entry-Level Pharmaceutical Quality Control and Regulatory Affairs Associate

I am a Bachelor of Pharmacy graduate with foundational knowledge of pharmacology, pharmaceutics, pharmaceutical chemistry, pharmaceutical analysis, GMP, and clinical research.

I am seeking an entry-level opportunity in quality control, regulatory affairs, clinical research, medical writing, or pharmacovigilance. I want to apply my knowledge of GMP, pharmaceutical compliance, analytical testing, and scientific documentation to support patient safety.

I have gained practical exposure to tablet and capsule manufacturing, including granulation and coating processes performed according to SOPs, GMP requirements, WHO guidelines, and pharmaceutical compliance standards.

I have experience assisting with the review and documentation of batch records, deviations, and change controls. I am familiar with pharmacopeial standards, stability testing methodologies, quality assessment techniques, and formulation development.

Through my academic project, I worked on the formulation and evaluation of an esomeprazole oral suspension for peptic ulcer treatment. I assessed pharmaceutical parameters including pH, drug-content uniformity, viscosity, redispersibility, stability, and acceptability.

I bring scientific writing, communication, problem-solving, teamwork, and basic data and document-handling skills. I am eager to contribute to a quality-focused pharmaceutical organization while continuing to develop my professional capabilities.