Summary
Work History
Education
Skills
Personal Information
Languages
References
Industrialtrainings
Research
Timeline
Generic

Hoor Fatima

Auburn,Australia

Summary

Master of Good Manufacturing Practices from University of Technology Sydney and Registered Industrial Pharmacist from VETASSESS and Successfully completed internship program with Cannim Group Australia, Sydney and Aegros Australia with well-versed Knowledge and experience in Manufacturing of pharmaceutical products, stability studies, packaging & labelling of drug products, Industrial pharmacy process validation, Quality Assurance/Control, testing of pharmaceutical drugs/products, and Goods Manufacturing Practices. And enhancing & accepting a challenging career in the field of Industrial Pharmacy Quality Assurance/Control, where in my theoretical knowledge and practical experience would be employed to the full potential and experience can be utilized in all aspects of business development as well as meeting organization objectives, with personal and professional growth.

Work History

Intern

Cannim Group
Manly, Australia
08.2024 - Current
  • Company Overview: Cannim established in 2017 and head quarter in Manly, NSW. Cannim ensures safety and pharmaceutical-grade quality while collaborating with EU GMP-certified manufacturers and research bodies. Serving markets in the USA, Canada, Europe, the UK, and Australia, Cannim is known for brands like Lumir.
  • My Tasks at Cannim:
  • Ensuring Quality and Consistency: Developing Standard Operating Procedure for Stability Study and Expiry Extension for Pharmaceutical Products as per PIC/S guide to GMP Part-I and PIC/S guide to GMP Part-II
  • Developing Training Metrics
  • Quality Control Laboratory Audit Checklist reviewing and updating the checklist according to ICHQ1A-R2 and ICHQ9 and TGA and FDA guidelines
  • Reviewing Labelling requirements according to latest TGA, TGO, ICHQ8 and FDA guidelines.
  • Website: http://www.cannim.com/

Worked as AMS Intern With Aegros Group Australia

Aegros
Macquarie Park, Australia
  • Ensuring of all pharmaceutical drugs and related supplies meets quality and regulatory standards and safe for their use
  • Conducting research to improve the quality of pharmaceutical products
  • To cater substantial recommendation for suitable changes to the manufacturing process for pharmaceutical products/drugs that fail to meet quality standards
  • Preparation of master formula Record, Batch Manufacturing Record, Master Packing Record & Batch Packing Records of all pharmaceutical drugs
  • To approve or reject raw materials, packing materials and intermediate, bulk and finished drugs/products in relation to their specifications at all phases of pharmaceutical drugs/products, manufacturing processes
  • Review & approve SOPs, Annual Product Quality Reviews & Validation Master Plan, Change Controls, deviations of the pharmaceutical products and their related processes
  • Periodic review of all quality functions such as Validation, Documentation, Training, QA, and QC, and procedure for appropriateness and review of related documents
  • To review & approve the investigation reports, Market Complaints, out of specifications & out of trends for the out-dated pharmaceutical drugs/products
  • Accountability for the development and all testing’s of new medications and the quality assurance and regulatory compliance of those medications

Intern

Aegros Membrane System
Sydney, Australia
  • Project Title: Analysis of Quality Control and Process Validation Data for Aegros Membrane System
  • Aim: To provide support in data analysis, reporting for QC methods and validation
  • Activities: To review and update URS, SOP using company templates
  • To collect data from manufacturing batch records
  • To collect and analyse data from QC results
  • Calculations for tolerance, formulation, engineering, etc
  • To prepare report on data analysis and recommendation

Education

Master of Goods Manufacturing Practices -

University of Technology Sydney
Sydney CBD, NSW, Australia
11.2024

Bachelor of Pharmacy - Pharmacy

Jawaharlal Nehru Technological University

Skills

  • Proficient in Good Manufacturing Practices
  • Drugs Stability Study
  • Enhanced Sustainability
  • Strong decision maker
  • Goods Manufacturing Practices (GMP)
  • Innovative
  • Service-focused
  • Expert in technical report writing and documentation work

Personal Information

  • Date of Birth: 09/07/92
  • Marital Status: Single

Languages

  • English
  • Hindi
  • Urdu

References

  • Reza Koochak, Head of Quality, Cannim Group, +61 470 424 405, reza@cannim.com
  • Dr. Kazi Mehzabeen, Process Engineer, Aegros, 0433311285, kazi.mehzabeen@aegros.com.au

Industrialtrainings

  • Complementary Medicine Group, 5A Jubilee Avenue, Warriewood, NSW, 2102, 2023
  • Linfox, 27-49 Lenore Drive, Erskine Park, NSW, 2759, 2024
  • Virbac, 2152 Castlereagh Road, Penrith, NSW, 2750, 2024
  • AstraZeneca, 47-Talavera Road, North Ryde, NSW, 2113, 2023
  • Richer Pharmaceuticals, Hyderabad, Hyderabad, Telangana, 500001, 2015

Research

Development and Evaluation of Gastro Retentive Floating of Simvastatin, STARTECH LABS, Hyderabad, Telangana, 500001, 2016

Timeline

Intern

Cannim Group
08.2024 - Current

Worked as AMS Intern With Aegros Group Australia

Aegros

Intern

Aegros Membrane System

Master of Goods Manufacturing Practices -

University of Technology Sydney

Bachelor of Pharmacy - Pharmacy

Jawaharlal Nehru Technological University

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Hoor Fatima