Christine is a Project Engineer based out of Cheme’s West Office where she has been involved in the project management, design, execution, and C&Q of improvements and upgrades on existing pharmaceutical manufacturing systems and utilities. She has experience in vaccine manufacturing, with projects focused on upstream and downstream manufacturing equipment. She has also worked on projects for CIP and SIP of those systems. With over 10 years experience in the pharmaceutical industry, Christine is well versed in GMP operations and has been involved in FDA audits. Additionally, she manages stakeholders and ensures projects are completed within the specified timeline to GMP standards.
Christine has a B.A.Sc from the University of Waterloo and a M.A.Sc from Ecole Polytechnique where she completed her thesis work at Canada’s National Research Council Human Health Therapeutics in Montreal.
“Cheme has a team with a wide range of experience that provides high quality work and pays close attention to all the details to ensure your project is successful. ”
Recent Success
Vaccine Manufacturing Process Upgrades Project
We partnered with our client in the biotechnology industry to design, optimize, implement, and validate their existing biologic manufacturing process.
Cheme was engaged to design and commission equipment to support a Major Component Replacement (MCR) project at one of the largest electricity suppliers in Ontario.
Our client needed to relocate a high throughput beverage quality assurance laboratory to a high-rise building location without disrupting business continuity. Learn how Cheme helped.
In Line Oil Winterization and Evaporation Production Suite Project
A pharmaceutical-grade botanicals oil producer approached Cheme to scale-up, design and optimize an existing multi-step extraction and winterization process.
A Canadian pharmaceutical client needed to expand manufacturing capabilities for oral solid dose production. Here’s how Cheme support our client’s execution of the manufacturing expansion.