Remote Pharmaceuticals Jobs · GMP

• Lead the development, validation, and commercialization of radiolabeled monoclonal antibodies and conjugates.
• Manage global bioprocess and bioconjugation teams, ensuring readiness for clinical production scale-up and commercial launch.
• Collaborate with internal and external partners, drive compliance with GMP standards, and contribute to regulatory filings and strategic decision-making.

The CMC Quality Manager, Analytical, provides quality oversight and technical leadership for analytical development and testing activities supporting veterinary pharmaceutical products under FDA Center for Veterinary Medicine (CVM) guidance. This role ensures that analytical methods, stability programs, and product testing are scientifically sound, validated, and compliant with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and applicable regulatory expectations.

Seeking a VP, Global Head of Quality to provide strategic leadership and executive oversight of all Quality functions across Kyverna’s global operations. Individual will be responsible for developing, implementing, and maintaining the GxP Quality framework supporting all Kyverna programs and ensuring the highest standards of quality, compliance, and patient safety throughout the organization.The VP will partner cross-functionally to define and embed a strong quality culture.