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Facilitate and lead cross-functional projects in a biotech manufacturing facility, managing key initiatives across various departments and ensuring regulatory compliance.

Lead the Manufacturing Science and Technology team to oversee processes from development to commercial operations, ensuring product quality and regulatory compliance.

Oversee revenue accounting processes, ensure compliance with ASC 606, lead revenue close activities, and partner with cross-functional teams.

Responsible for securing favorable coverage and reimbursement for Orca Bio products by engaging with payers and hospitals, ensuring patient access and navigating payer policies.

Manage quality systems, including deviations and CAPAs. Ensure quality standards before product release and maintain compliance with regulatory requirements.

As a Quality Control Scientist, you will ensure microbiological safety, conduct testing and assessments, implement control measures, and support regulatory compliance in biopharmaceutical manufacturing.

Lead the onboarding and market enablement for Orca Bio's therapies, ensuring operational readiness and engagement with treatment centers, while developing processes and working cross-functionally with clinical and commercial teams.

The Analyst will manage data reporting infrastructure and analytics tools, delivering insights for sales and operational performance. This includes building data ecosystems and supporting commercial analytics across teams.

The Director leads US market access strategy for cell therapy, developing reimbursement tactics and collaborating with cross-functional teams to optimize patient access and value propositions.

The Manager, Global QMS will oversee Orca Bio's Quality Management System, ensuring compliance and alignment across sites. Responsibilities include leading audits, managing supplier qualifications, and improving quality systems with cross-functional collaboration.