India
I am an aspiring Regulatory Affairs professional with an academic background in MSc Biotechnology and ongoing training through an Advanced Diploma in Clinical Research. I am deeply interested in drug compliance, patient safety, and global regulatory frameworks that ensure the quality, safety, and efficacy of medicinal products. My learning and exposure cover regulatory documentation, ICH-GCP principles, clinical research processes, and pharmacovigilance fundamentals, giving me a holistic understanding of regulatory expectations across the product lifecycle. I bring a detail-oriented, compliance-driven mindset with a strong focus on accuracy, timelines, and regulatory standards. I am actively seeking an entry-level Regulatory Affairs opportunity where I can apply my knowledge, gain hands-on regulatory experience, and contribute to compliant regulatory operations while growing under experienced regulatory professionals.
Maintained accurate records and documentation while adhering to predefined guidelines and instructions. Performed quality checks to ensure consistency, completeness, and compliance with internal standards. Worked closely with supervisors and team members within structured workflows. Demonstrated strong attention to detail, time management, and communication skills.