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Oversee and implement effective Legal & Compliance Program, support leadership, drive anti-bribery initiatives, and manage compliance projects.

The role involves managing GxP lab systems, ensuring compliance, supporting system lifecycles, and leading projects in the analytical labs.

Design, execute and report scientific experiments in biopharmaceutics, manage lab activities and lead a team in pharmaceutical therapies development.

Lead statistical programming for clinical trials, ensuring quality deliverables, managing teams, and collaborating cross-functionally. Responsibilities include auditing readiness and providing strategic technical guidance.

Lead statistical programming activities, ensure quality and timely deliverables for clinical studies, collaborate with cross-functional teams, and review programming aspects in compliance with industry standards.

The Director/Sr Director of Biostatistics leads statistical strategy in drug development, collaborates across functions, and mentors other statisticians.

The Manager oversees the Data Integrity Program, ensuring compliance in Quality Engineering, and manages the regulatory CMC activities at the site while promoting a Data Integrity culture and resolving compliance issues.

The Quality Assurance Engineer ensures compliance, supports product manufacturing audits, and maintains GMP standards in gene therapy facilities, overseeing validation and operational quality.

The Senior Quality Assurance Engineer ensures compliance and quality of gene therapy manufacturing, supports audits, and oversees validation processes.

The role involves managing engineering activities, including maintenance coordination, project execution, and compliance with safety and quality standards, while supporting audits and facilitating engineering improvement projects.