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The Specialist in Global Procurement - Supplier Quality Compliance supports cGMP compliance by maintaining procurement procedures, coordinating supplier audits, managing compliance documents, and assisting with Supplier Corrective Action Reports while fostering stakeholder relationships.

As a Project Manager at Regeneron, you will coordinate and manage various projects, congresses, and events. Responsibilities include administering promotional activities, maintaining internal control processes, and supporting the sales organization. You will also manage sales meetings, onboarding of new team members, and provide direct support to the Country Manager.

The Commercial Operations Manager will support decision-making through analysis, maintain sales tools like Veeva CRM and Tableau Dashboard, lead analytics projects, track performance metrics, and communicate findings across departments while enforcing company policies.

The QA Investigation Specialist is responsible for conducting investigations into non-conformance issues and implementing corrective actions for manufacturing operations. This role includes preparing reports, analyzing data, ensuring compliance with cGMP standards, and collaborating with cross-functional teams to enhance quality processes.

The Senior Administrative Coordinator provides high-level administrative support to the Senior Vice President of Global Immunology. Responsibilities include managing calendars, coordinating meetings and travel logistics, expense reconciliation, and maintaining confidentiality. The role requires strong organizational skills, critical thinking, and effective communication to interact across all levels of the organization.

The Associate Manager, Quality Assurance (MES) supervises a QA team, ensuring compliance and quality in manufacturing processes, managing documentation approvals, and participating in regulatory audits. They focus on meeting goals for MES implementation and provide leadership in improving QA performance.

As a Quality Control Technical Resources Specialist, you will manage validation and qualification projects, collaborate with teams, write protocols, control test procedures, and communicate with management and partners on progress and discrepancies. You will thrive in a fast-paced environment, handling multiple tasks and driving scientific improvements.