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Careers

Development Engineer/Scientist I (Media Development/Metabolomics/Proteimics)

CCRM

As a Development Scientist (DS), 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 be responsible for metabolic and proteomic data analysis for the development of custom-media formulation as well as lead the data analysis function for other scientific areas. The DS will define a solution space for media composition based on deep understanding of metabolic biochemistry, media component interactions, growth factor requirements and advanced analytical outputs.

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Human Resources Manager, Talent Acquisition and Development

CCRM

As CCRM’s Human Resources (HR) Manager, you will report to HR leadership and will be part of a team supporting a dynamic growing organization focused on developing and commercializing cell and gene therapies and regenerative medicine technologies. You will provide assistance through the Talent Acquisition cycle; working with leaders and business units to recruit, screen, interview candidates, and guide Employee Development for CCRM; ensuring the development, delivery and outcomes of learning strategies and training programs meet organizational objectives and individual employee development interests. 

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Quality Assurance Associate I

CCRM

As a Quality Assurance Associate at CCRM you will be part of a diverse bioengineering team focused on designing and implementing quality management initiatives or programs 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. You will be a quality leader 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 Assurance Associate II

CCRM

As the Quality Assurance Associate II at CCRM, you are a seasoned individual in the field of 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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