The Training Coordinator facilitates daily training operations, maintaining training records and compliance with GMP. Responsibilities include managing training curriculum, scheduling sessions, preparing reports, and supporting employee training, ensuring adherence to regulatory standards.

The QMS Administrator will manage the MasterControl QMS platform, oversee document control, ensure compliance with standards, support audits, provide training, and identify improvements in QMS processes. Collaboration with various departments and reporting on QMS performance will be essential responsibilities.

The Full Stack Developer will design, develop, test, and maintain software applications for the medical industry, ensuring compliance with industry standards. Responsibilities include working with technologies such as C#, SQL, Java, AWS, and leading best practices in software development.

The Head of Field U.S. Market Access will lead and build a US Payer Field Team focused on ensuring patient access to cell therapies, driving revenue and market positioning. Responsibilities include strategic leadership for market access strategies, pricing, payer research, and team development to support product launches and lifecycle management.

As the Head of Legal at Orca Bio, you'll provide comprehensive legal counsel on corporate governance, financing transactions, regulatory compliance, and contract operations. You'll manage due diligence, draft agreements, represent the company in legal matters, and oversee outside counsel. This role necessitates significant experience in corporate law, particularly in the life sciences sector.

The Quality Assurance Representative will manage quality systems, handle deviations, implement CAPAs, document management, evaluate batch records, ensure compliance with regulations, prepare for audits, and provide training to staff, while collaborating with cross-functional teams in a biotech setting.