Rased

Senior Deputy Manager – Quality Assurance

Renata Limited • Full-time

Mar 2018 - Present • 8 yrs 7 mos

Pharmaceutical Quality Assurance professional with 10+ years of experience in the pharmaceutical industry, specializing in GMP, Quality Management Systems (QMS), validation, qualification, regulatory compliance, audits, and pharmaceutical documentation. My professional experience includes SOP development, review, revision, and implementation; CAPA management; deviation investigation; OOS/OOT investigation; change control; risk assessment and FMEA; APQR/PQR; data integrity and ALCOA+; equipment and process qualification; validation protocols and reports; batch documentation review; GMP audit preparation; and quality system improvement. I have practical knowledge of major international pharmaceutical regulations and guidelines, including WHO GMP, US FDA, EU GMP, UK MHRA, PIC/S, and ICH. I am experienced in preparing clear, compliant, and well-structured pharmaceutical documents suitable for quality systems and regulatory requirements. In addition to pharmaceutical QA services, I provide professional data entry and documentation support, including Microsoft Excel, Google Sheets, data cleaning, data formatting, PDF-to-Excel/Word conversion, web research, document review, and document formatting. My strengths include attention to detail, accuracy, confidentiality, analytical thinking, regulatory awareness, and timely delivery. I focus on understanding each client's requirements and providing practical, reliable, and high-quality work. I am available to support pharmaceutical companies, QA/QC professionals, consultants, researchers, small businesses, and individual clients who need dependable pharmaceutical quality, documentation, data management, and virtual assistance services.