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.

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.

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

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

Develop and maintain software quality assurance processes for medical devices, ensuring compliance with regulatory standards and conducting system validations.

Develop and maintain software quality assurance processes for non-product software in medical device development, ensuring regulatory compliance and continuous improvement.