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Manage the day-to-day operations of HCP engagement, contracting processes, and maintain compliance and documentation standards while supporting internal stakeholders.

The Associate Director is responsible for overseeing global labeling processes, ensuring compliance, collaborating with teams, and managing documentation for drug products.

The Director of Global Quality GMP Processes leads the optimization of quality processes, ensuring compliance with GMP and regulatory standards, and promotes continuous improvement in product quality across regions.

Manage end-to-end contracts for Global Medical Affairs, including drafting, negotiating, and ensuring compliance. Liaise with vendors and stakeholders, oversee vendor performance, and implement process improvements.

The Associate Director will oversee quality operations, drive efficiency, manage risks, ensure compliance, and lead process improvement initiatives in a global quality organization.

The Senior Director of Global Quality Solutions drives efficiency in quality processes through automation, leading digital transformation initiatives, managing projects, and fostering innovation in document management.

The Senior Manager oversees quality assurance for biologics manufacturing, ensuring compliance with GMP standards, managing contract manufacturers, and leading quality system records for clinical and commercial products.

Oversee development and optimization of customer engagement platforms; manage team, leverage data insights, and align initiatives with corporate strategies.

The Executive Director oversees US market access strategies and marketing for Otsuka's CNS portfolio, leading a team and collaborating across functions to ensure strategic alignment and effective service delivery to U.S. payers and customers.

Oversee quality of clinical and commercial controlled substances, ensuring compliance with cGMP and regulatory standards, while driving continuous improvement across global Otsuka operations.