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The Process Engineer I leads bioprinting manufacturing processes and validates drug products while adhering to regulatory guidelines and industry standards.

Develop and optimize cryogenic preservation processes for Bioprinted Tissue Therapeutics, collaborating across teams to ensure product viability and compliance with regulations.

Lead experimental strategy in immunoengineering, developing bioprinted tissue therapeutics and collaborating across disciplines. Oversee in vitro and in vivo studies, integrating immunology insights into product design.

Lead a histology team and contribute to bioprinted therapeutic programs by planning experiments, analyzing data, and collaborating with scientists and engineers.

The Senior Associate, QC Analytics will perform analytical testing, ensure compliance with regulations, and support product development for biotherapeutics.