SONAM GYALPO

Precise Quality Assurance Inspector with a distinguished understanding of detail-oriented inspections and commitment to high standards. Successful at staying focused after long hours of inspections and detailed recordkeeping. Analytical Quality Assurance Inspector with over 5 years of experience. Fantastic eye for detail with high-standards of final products. Committed to detailed recordkeeping and coworker collaboration. Talented Quality Control Inspector driven to improve product quality in manufacturing environments. Provider of relevant and effective product and component tests. Eager to help manufacturers eliminate production errors and increase successful manufacturing figures. Hardworking Quality Control Inspector offering over years of manufacturing and production experience. Detail-oriented and systematic professional knowledgeable about compliance standards. Adheres strictly to documentation guidelines and reporting requirements. Highly-motivated employee with desire to take on new challenges. Strong worth ethic, adaptability and exceptional interpersonal skills. Adept at working effectively unsupervised and quickly mastering new skills.

• Safety Education Activities Performing several manual and automated quality assurance checks on raw materials, in-process products, and finished products. Reviewing documents to ensure that they completed in accordance with current GMP and site SOPs. Initiate events and investigation reports for any problems or deviations found during inspection. Collect samples and inspect components, drug product containers, packaging and labeling according to approved written material specifications. Inspect product operations for each new control per product line and initial line inspections to assure the identity, quality, and traceability of incoming product materials according to current SOPs. Generate Logbooks, investigation reports, Notice of incident Reports, and CAPA reports. Perform AQL sampling inspections of finished products and tighten quality inspections, as necessary. Review quality procedures, batch records, in process test results, and AQL attribute inspections. Revise and review (SOP) and samples test protocols Follow GMP documentation practices in manufacturing and packaging batch records. Departments that I have worked in are – Raw material, Labeling control, Pharmacy, Granulation, Mixing, Compression, Encapsulation, Soft-gel and hard Gelatin, Packaging Line, etc.
• Languages English Nepali Tibetan Hindi Urdu