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This role manages pharmacovigilance agreements with business partners, ensuring compliance and maintaining effective business relationships, while supporting QMS in audit processes.

This role involves negotiating and managing IT service contracts, ensuring compliance and fostering vendor relationships, while driving organizational alignment.

Provide administrative support to National Sales Lead and Market Access team, including managing contracts, budgets, meetings, and communications. Coordinate projects and promote effective records management.

The Specialist, Quality Engineer ensures compliance with quality systems, oversees documentation, and collaborates with cross-functional teams to maintain GMP operations, focusing on quality oversight and regulatory adherence.

The Validation Manager will oversee validation programs for a cGMP Cell Therapy Manufacturing facility, manage a team, and ensure compliance with regulations and standards.

The Identity Management Engineer will manage IAM operations, enhance access governance, support integrations, and ensure secure identity lifecycle management across multiple platforms.

The Translational Bioinformatics Lead will spearhead bioinformatics strategy for drug discovery and development, conducting analyses to guide patient selection and biomarker identification, while managing data from clinical trials.

The Specialist, R&D System Support handles access management, data model support, and process optimization for R&D systems, collaborating with teams and stakeholders.

The Process Engineer supports deployment and troubleshooting of equipment and processes in drug manufacturing, collaborating across functions to enhance efficiency and compliance.

The role is for a Senior BI Architect specializing in Qlik, but specific responsibilities were not provided.