Industrial Pharmaceutical & Bio-Pharmaceutical Quality Control and Quality Assurance

Industrial-Pharmaceutical-Bio-Pharmaceutical-Quality-Control-and-Quality-Assurance2

This comprehensive diploma program has been developed to meet the skills requirement for effectively performing duties in quality control, quality assurance, method development and method validation fields in Pharmaceutical/Bio- Pharmaceutical industries for those who want to upgrade existing skills or obtain new skills. Each area of the study will be covered in an in-depth manner for both Pharmaceutical and Bio-Pharmaceutical sectors.

Program Starts: Fall, Spring, Summer & Winter

Admission Requirments: Minimum of Grade 12 Diploma,  Minimum of Grade 12 Diploma with required science and math courses/Equivalent.

The program includes the following applications:

This course will introduce the concepts and requirements necessary for compliance with Good Manufacturing Practice (GMP) and Good Clinical Practice (GCP) for pharmaceuticals and biopharmaceuticals. It will prepare students to establish and document a system of GMP controls required to manufacture drug products in Canada, the United States and in many parts of the world. It focuses on real work industrial scenarios.

This course will introduce the concepts and requirements necessary for compliance with Good Laboratory Practice (GLP) for pharmaceuticals and biopharmaceuticals. It will address the most important laboratory techniques. Students will also get exposure and experience with all major pharmaceutical instruments. It focuses on real work industrial scenarios.

This course will introduce dissolution current testing practices, testing requirements, critical components, sample preparation techniques, media preparation, sample testing, data analysis, report preparation, limitations, IQ/OQ/PQ, calibration, trouble shooting, maintenance, and out of specification investigation.

This course will introduce HPLC theory, components, testing practices, testing requirements, sample preparation techniques, mobile phase preparation, sample testing, data analysis, report preparation, limitations, IQ/OQ/PQ, calibration, trouble shooting, maintenance, and out of specification investigation.

This course will introduce gas chromatography history, concepts, carrier gas, testing requirements, critical components, sample preparation techniques, sample testing, data analysis, report preparation, limitations, IQ/OQ/PQ, calibration, trouble shooting, maintenance, and out of specification investigation.

This course will introduce how to initiate and perform method development and method validation using the HPLC /UV Spectrometer and the Dissolution Apparatus. It will cover major industrial regulations in terms of developing and validating testing methods.

This course will introduce how to initiate and perform method development and method validation using the GC /UV Spectrometer. It will cover major industrial regulations, in terms of developing and validating testing methods.

This course will introduce different types of writing and compiling scientific documents in QC and QA areas: SOPs, communication methods and issues, method validation reports writing, method validation protocols writing, dealing with batch records, auditing reports, investigations, and real work industrial scenarios.

 

Course Highlights:

  • 26 weeks Program
  • Hands-on Training
  • Optional Job Assistance for co-op, internship and full-time opportunities within pharmaceutical and bio-pharmaceutical and related sectors

Job Opportunities in Multiple Areas:

Technologists, Raw Material Chemists, Finish Product Chemists, Stability Chemists, R&D Chemists, Scientists, Calibration Chemists, Document Reviewers, Laboratory Coordinators, Trainers, SOP Writers, Auditors, Supervisors, and Managers.