Naghma Saeed Email & Phone Number

Markham, Ontario, Canada

Finished product GMP quarantine and releaseStrong QA documentation and reporting skillsReviewing and approving cGMP SOPsChange Control ManagementAnalyzing internal and external deviationsRoot Cause Analysis TechniquesPropose and manage Corrective and Preventive Actions (CAPA) Experience in GMP and GVP auditsSelf-InspectionRisk Management and Risk MitigationGMP Training

Toronto, Canada Area

Prepared food and beverages according to the quality standards set forth by the companyMaintained electronic log books to monitor the temperature and expiry of all food productsKept track of produce expiry and discarding process in order to meet quality standards throughout Organise and replenish various shelves neatly

Toronto, Canada Area

Prepared mobile phase and conduct assay test using HPLC coupled with UV-Vis and PDA detectorsPerformed dissolution testing on R&D batch of drugs including buffer preparation, sampling and testing Performed raw material and finished product tests following SOPsAssisted in preparing analytical test reportsAssisted QA/QC Associate in performing tests for ongoing stability studies which successfully led to achieve targeted accuracyParticipated in internal investigations of OOS results Increased work efficiency by organizing chemical reagents alphabetically in lab cabinets and kept track of material inventoryAdhere to SOPs and practiced cGMP and GDP on daily basisMaintain real-time entries in the lab books and log books

Pakistan

Designed medical report templates for radiologists in the US Reviewed and edited transcribed reports for spelling, grammar, clarity, consistency, and proper medical terminologySuccessfully maintained quality benchmark through continuous supervision of medical transcriptionistsReceived appreciation by USA-radiologists on transcribing error-free medical reports

Pakistan

Prepared mobile phase, standard and sample solutionsMonitored testing of various raw materials, active pharmaceutical ingredients and finished products performed according to SOPsAssisted in analytical testing and maintained daily logs and results of the tested raw materials and active pharmaceutical ingredientsLabeled and tagged the secondary reagent containers, specifically mentioning the reagent’s name, hazard and expiry date

Post Graduate Diploma, Pharmaceutical Quality Assurance & Quality Control

PHARMACEUTICAL HANDS-ON TRAINING Quality Control • Proficient in processing and integrating chromatographic data using Empower software •.

Master'S Degree, Analytical Chemistry, 1St Division

Bachelor'S Degree, Chemistry, Cgpa: 3.4