Fatima John Email & Phone Number

Windsor, Ontario, Canada

In my role, I support all Quality Systems to ensure our products are manufactured according to current Good Manufacturing Practices (cGMP). I assist other departments with quality and GMP issues, ensuring compliance with all relevant regulatory requirements. I am accountable for the timely release of materials and products to cGMP standards, meeting the company's Quality standards. Aside from these, internal audits, product complaint investigations, deviations & trending, out of specification investigations, vendor/raw material qualifications, environmental trending, are some of the other QA/Compliance/Regulatory - related tasks that I perform in my job.

Whitby, Ontario, Canada

My work in the Pharma Development Services Group involved optimizing and validating protocols to ensure accuracy, precision, and reliability, contributing to the successful development and manufacturing of pharmaceutical products.

Toronto, Canada Area

Extensive experience in testing raw materials, finished products, and conducting stability testing.

Mumbai, India

Study of non-specific metal-protein interactions for applications in Nanotechnology

Mysore

Isolated immunomodulatory proteins and lectins using Chromatography techniques.Developed an ELISA-based assay similar to ELISA for protein detection using lectins.Conducted both in vitro and in vivo proliferation studies.

Bengaluru Area, India

Chromatography for purification of Rotavirus recombinant protein, NSP4

Research Doctorate, Physicochemical And Functional Characterization Of The Immunomodulatory Proteins From Allium Sativum

Activities and Societies: Indian Immunology SocietyIsolated proteins from plant sources, characterized, and studied their.

Post-Graduate Diploma In Pharmaceutical Quality Assurance And Quality Control

Master Of Science, Biotechnology

Pharmaceutical Quality Assurance And Quality Control