Naghma Saeed

QA Specialist at Probus Logistics
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Contact Information
us****@****om
(386) 825-5501
Location
North York, Ontario, Canada, CA

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Experience

    • Canada
    • Transportation, Logistics, Supply Chain and Storage
    • 1 - 100 Employee
    • QA Specialist
      • Nov 2022 - Present

    • Canada
    • Transportation, Logistics, Supply Chain and Storage
    • 100 - 200 Employee
    • QA Associate/QPIC
      • Apr 2020 - Oct 2022

    • Canada
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Quality Assurance Associate
      • Jun 2018 - Apr 2020

      Finished product GMP quarantine and release Strong QA documentation and reporting skills Reviewing and approving cGMP SOPs Change Control Management Analyzing internal and external deviations Root Cause Analysis Techniques Propose and manage Corrective and Preventive Actions (CAPA) Experience in GMP and GVP audits Self-Inspection Risk Management and Risk Mitigation GMP Training Finished product GMP quarantine and release Strong QA documentation and reporting skills Reviewing and approving cGMP SOPs Change Control Management Analyzing internal and external deviations Root Cause Analysis Techniques Propose and manage Corrective and Preventive Actions (CAPA) Experience in GMP and GVP audits Self-Inspection Risk Management and Risk Mitigation GMP Training

    • Canada
    • Food and Beverage Services
    • 700 & Above Employee
    • Team Member
      • Jun 2016 - Nov 2018

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

    • Canada
    • Higher Education
    • 1 - 100 Employee
    • QA/QC Lab Volunteer
      • Jul 2017 - Feb 2018

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

  • Careline
    • Pakistan
    • Document Reviewer
      • Jul 2011 - Mar 2016

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

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Intern
      • Jun 2012 - Jul 2012

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

Education

  • TIPT
    Post Graduate Diploma, Pharmaceutical Quality Assurance & Quality Control
    2017 - 2017
  • Karachi University
    Master's degree, Analytical Chemistry
    2011 - 2012
  • Jinnah University for Women
    Bachelor's degree, Chemistry
    2008 - 2009

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