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Courses/Engineering/Chemical Engineering

Advanced Engineering: Quality Assurance & Quality Control

Mastering Excellence in Pharma Engineering: Navigating Quality, Compliance, and Regulatory Challenges

Created byTina Dolatzadeh
4.8
(4 reviews)
AdvancedUpdated Nov 20, 2023
Advanced Engineering: Quality Assurance & Quality Control

What You'll Learn

check_circleUnderstand Quality Assurance and Control: Grasp the significance and methodologies of quality assurance and control in pharmaceutical manufacturing.
check_circleNavigate Regulatory Landscapes: Effectively understand and apply the regulatory requirements of Health Canada and the FDA in pharmaceutical practices.
check_circleComprehend Quality Management Systems: Acquire detailed knowledge about the implementation and significance of QMS in the pharmaceutical industry.
check_circleManage Pharmaceutical Ingredients: Understand the challenges and regulations surrounding APIs and other ingredients in pharmaceuticals.
check_circleEnsure Instrument and Process Quality: Apply knowledge of process qualification and instrument quality in manufacturing.
check_circleHandle Data with Integrity: Manage and maintain the integrity of data in pharmaceutical processes.
check_circleApply Risk Management Principles: Utilize risk management methodologies effectively in quality assurance.
check_circlePrepare for Regulatory Audits: Develop skills and strategies for successful preparation and handling of regulatory audits and inspections.

About This Course

This intensive course is designed for engineers in the pharmaceutical industry, focusing on the critical aspects of quality assurance, quality control, and regulatory compliance. It covers the intricate details of pharmaceutical manufacturing standards in Canada and the United States, highlighting the importance of quality management systems, active and non-active ingredients, filler ingredients, and the nuances of Canadian and American pharmaceutical standards. Participants will gain in-depth knowledge about Health Canada and FDA regulations, process validation, data management, risk management, and the complexities of pharmaceutical documentation and audit readiness. 

Key Topics Discussed: 

- Quality Assurance and Control in Pharmaceutical Manufacturing: Understanding the fundamental concepts and importance of quality assurance and control in the pharmaceutical sector. 
- Regulatory Compliance: Navigating and complying with Health Canada and FDA standards, focusing on differences and similarities between Canadian and American pharmaceutical regulations. 
- Quality Management Systems (QMS): Detailed study of QMS and their role in ensuring quality in pharmaceutical practices. 
- Active Pharmaceutical Ingredients (APIs) and Fillers: Challenges and regulations associated with APIs, fillers, and other pharmaceutical ingredients. 
- Instrument Quality and Process Qualification: Ensuring quality and reliability in manufacturing processes and equipment. 
- Data Management and Integrity: Strategies for managing pharmaceutical process data, ensuring its accuracy and integrity. 
- Risk Management Methodologies: Applying methodologies like FMEA and HAZOP in quality assurance. 
- Preparation for Regulatory Audits and Inspections: Best practices and strategies for handling audits and inspections by regulatory bodies.

Your Instructors

Tina Dolatzadeh
Tina Dolatzadeh

Professional Engineer in Pharma and STEM Industries

menu_book1 courses
star4 reviews

As a licensed Professional Engineer with 20 years of experience in chemical engineering, I bring a unique blend of expertise across science, Operational Excellence, project management, and entrepreneurship. My career has spanned a range of industries, from pharmaceuticals and polymers to engineering design, leadership, and academia. I am certified as an ASQ Six Sigma Green Belt and hold a designation as a Project Management and Operational Excellence Leader. I’m passionate about driving innovation, enhancing processes, and delivering measurable results that add value across diverse fields.

Darryl Johnson II
Darryl Johnson II

Host

Darryl Johnson II is a creative thinker based in sunny Southern California. A prolific content creator, he has published several dozen works for wind band, jazz band, and orchestra and is the author of dozens more print and multimedia publications in both the fiction and non-fiction categories. Along the way, he has delivered academic presentations to hundreds of schools in over 40 states and 3 countries and has received regular laudits for a supportive and relatable approach to education. A composer of music and a composer of words, Darryl Johnson II has developed an insatiable interest in a broad range of concepts and ideas that have been refined by fires of art and strategy and he is passionate about inviting others on new and interesting journeys of thought, experience, and design.

Credit Information

Do these courses count toward my professional development requirements?

This portal is provided as a training and development resource for City of Markham employees. Every course is delivered by a qualified subject matter expert or learning organization, is quantifiable in hours, and is verifiable — you receive a documented certificate of completion for every course you finish, stored on LearnFormula indefinitely.

If you hold a professional designation (for example in engineering, accounting, human resources, or law), courses may be counted as professionally relevant, verifiable learning activities toward your continuing professional development. Individual practitioners are responsible for confirming that an activity meets the requirements of their professional body. For questions about the City of Markham's training and development policies, please speak with your people leader or Human Resources.

What Students Are Saying

4.8
Student's Choice
4 reviews

Frequently Asked Questions

We are a registered provider with 327+ associations and regulatory bodies worldwide. We operate across 29 global markets including Canada, the US, Australia, and the UK. Every course page clearly displays its specific accreditations. Upon completion, you receive a professional certificate that can be validated online. Our certificates include all necessary accreditation details, credit hours, and completion dates, and are formatted specifically to meet the submission requirements of most global regulatory bodies.