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Careers

Development Engineer/Scientist (Media Formulation)

BridGE

CCRM is looking for a Development Engineer/Scientist (DES). You will be part of a diverse bioengineering team focused on defining and executing process optimization and technology development projects within the cell and gene therapy and regenerative medicine fields. You will advance and implement processes for the production of optimized cell culture media. The DES will develop and optimize media and supplementation formulations based on deep understanding of cellular metabolism, component formulation and interactions, signaling requirements, and a mechanistic understanding of the underlying biology

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Operations Manager

Deliver - GMP Contract Manufacturing

As the Operations Manager at CCRM within the Deliver business unit, you are a seasoned individual in the field of Good Manufacturing Practices (GMP) manufacturing of cell and gene therapy products and regenerative medicine technologies, who is driven by the opportunity to enable their clinical translation. You will lead and develop CCRM’s manufacturing services, including fee-for-service work, contract manufacturing, access services, technology transfer, and technical and process development services to cell and gene therapy and regenerative medicine producers. You will provide technical expertise and will be responsible for customer engagement and communicating to customers, senior leadership, personnel and management, and will ensure the high-quality delivery of contract services. You will be a leader in understanding how to overcome cell and gene therapy manufacturing challenges to enable life-saving advances in regenerative medicine.

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Process Development Engineer/Scientist

BridGE

As a Process Development Engineer/Scientist you will be part of a diverse team focused on defining and executing process and technology development projects in cell and gene therapy. You will provide hands-on expertise in the manufacturing of human cells and will be responsible for overseeing the design and prototyping of innovative tools, technologies, and processes to address cell manufacturing workflow challenges.

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Quality Assurance Technician

Deliver - GMP Contract Manufacturing

As the Quality Assurance Technician in CCRM’s Deliver business unit, you are an experienced individual in the field of good manufacturing practices (GMP) manufacturing of biologics, or cell and gene therapy products, who is driven by the opportunity to enable clinical translation of cell therapy and regenerative medicine. You will lead and develop CCRM’s quality assurance and quality control teams to deliver on client demands, including fee for service work, contract manufacturing, access services, technology transfer, training and technical and process development services to cell and gene therapy and regenerative medicine producers. You will provide technical expertise and will be responsible for client audits, communication to customers, leadership, personnel and management and will ensure the high-quality delivery of contract services.  You will be a leader in understanding how to overcome cell manufacturing and testing challenges to enable life-saving advances in cell and gene therapy and regenerative medicine.

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Quality Control Associate I

Advance

As a Quality Control Associate I at CCRM you will be part of a diverse bioengineering team focused on designing and implementing a quality management program within the cell and gene therapy and regenerative medicine fields. You will provide technical expertise and will work within the team to define and execute project tasks, as well as day-to-day operational duties. You will be a quality control (QC) team member in bringing new and innovative products to market to enable life-saving advances in cell and gene therapy and regenerative medicine.

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Quality Manager

Deliver - GMP Contract Manufacturing

As the Quality Manager at CCRM-Deliver, you are a seasoned individual in the field of Good Manufacturing Practices (GMP) manufacturing of cell and gene therapy products, who is driven by the opportunity to enable clinical translation of cell therapy and regenerative medicine. You will lead and develop CCRM’s quality assurance and quality control teams, to deliver on client demands, including fee for service work, contract manufacturing, access services, technology transfer, training and technical and process development services to cell and gene therapy and regenerative medicine producers. You will provide technical expertise and will be responsible for client audits, communication to customers, leadership, personnel and management, and will ensure the high-quality delivery of contract services.  You will be a leader in understanding how to overcome cell manufacturing and testing challenges, to enable life-saving advances in cell and gene therapy and regenerative medicine.

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Vice President, Commercialization

Build

About CCRM: CCRM is a Canadian, federally incorporated, not-for-profit organization dedicated to supporting the development of foundational technologies that accelerate the commercialization of stem cell and biomaterials-based technologies and therapies. For more information about CCRM, please visit our website at http://www.ccrm.ca. Responsibilities: Proprietary Development...Read More