Engage in GMP regulatory compliance as a Quality Senior Specialist, supporting raw material disposition for late-stage biologics. Collaborate cross-functionally to ensure quality and efficiency in manufacturing operations, driving process improvements.

Optimize the quality assurance process for raw material disposition in GMP manufacturing. Collaborate with cross-functional teams to ensure compliance, enhance operational efficiency, and support the production of biotherapeutics while maintaining the highest standards.

Optimize your career as a Principal Process Engineer, leading complex projects, collaborating with experts, and driving innovative solutions in biotherapeutics manufacturing to enhance global access and improve processes seamlessly.

The Quality Risk Manager at Just Evotec Biologics is responsible for overseeing the quality risk program at the Redmond and Seattle sites, ensuring compliance with the Just Pharmaceutical Quality System and regulations. This role involves facilitating risk assessments, managing the site risk register, and collaborating with cross-functional teams to identify and mitigate risks.

The Quality Risk Manager at Just Evotec Biologics is responsible for overseeing the quality risk program at the Redmond and Seattle sites, ensuring compliance with the Just Pharmaceutical Quality System and regulations. This role involves facilitating risk assessments, managing the site risk register, and collaborating with cross-functional teams to identify and mitigate risks.