Jobs at Katalyst CRO

Designs and codes SAS programs for clinical projects, ensures regulatory compliance, and conducts quality control checks for clinical trial data.

Lead and execute packaging projects in pharmaceutical R&D, manage project complexities, develop protocols, and collaborate with teams to improve packaging processes.

The Supplier Quality Engineer selects, evaluates suppliers, conducts audits, performs process qualifications, leads problem resolution, and monitors supplier performance to ensure quality and compliance in medical device production.

Lead NPI activities for embedded software testing in medical devices, ensuring compliance with regulations, while managing teams and communicating with stakeholders.

The Scientist III will initiate a lentiviral delivery platform for gene therapy, collaborating with teams, designing vectors, and managing CRO production while ensuring compliance and productivity.