The Manager Statistical Programmer will lead and support programming activities, ensuring timely and high-quality results across multiple studies. Responsibilities include coordinating programming documentation, acting as a resource for programming standards, supporting regulatory submissions, and mentoring junior programmers.

The Sr. Manager of Supply Operations will lead and improve the supply chain and manufacturing operations while ensuring effective communication with internal and external partners. Responsibilities include overseeing supply orders, mitigating risks, and fostering partnerships to enhance operations.

The Senior QC Scientist will conduct assay validation and provide technical guidance for QC testing and assay development. Responsibilities include reviewing test procedures, participating in regulatory inspections, and contributing to cross-functional improvement initiatives. A strong background in microbiology, chemistry, or biology, along with experience in the pharmaceutical or biotechnology industries, is required.

The General Marketing Supervisor will oversee compliance with Japanese laws, manage local licenses, liaise with authorities, guide quality systems, and maintain stakeholder relationships to ensure business success in Japan.

The Associate Director, Global Procurement will lead procurement activities for the Clinical Drug Supply & Logistics category, manage supplier relationships, drive cost savings, and implement category strategies aligned with business needs. This role requires building influential relationships, running cross-functional teams, and having expertise in the biopharmaceutical market dynamics.

The Principal IT Business Analyst serves as a liaison between IT management and business partners to document and analyze business processes, identify requirements for new technologies, and support project implementations while ensuring alignment with organizational standards.

The Sr. Manager in Downstream Sciences leads a team assessing raw material changes impacting manufacturing. Responsibilities include risk assessments, managing projects, setting goals, ensuring compliance, and overseeing technical operations. The role also involves collaborating with other departments and participating in audits.

The Sr. Manager Development Program Management leads operational direction for drug development programs, overseeing program planning, budgeting, and timelines. They manage cross-functional teams, assess needs from preclinical to commercialization, and drive strategic goals while fostering collaboration and effective communication across teams. They also implement risk mitigation strategies and champion process improvements in development.

The Associate Director, IT Operational Technology oversees the operational activities of the IT/OT infrastructure, ensuring reliable operations, managing teams, and coordinating IT projects. Responsibilities include compliance with regulations, security management, and developing IT strategies that align with organizational goals.

The Senior Manager, Executive Technology Support oversees the IT and A/V infrastructure for senior leaders, ensuring reliable operation and support for executive events. Responsibilities include managing A/V service providers, troubleshooting technical problems, providing project management for new equipment, and maintaining support metrics. The role involves extensive interaction with senior management and oversight of A/V resources for meetings and events.

The IT Business Management Analyst supports core business services, manages communications, assists in resource management, and contributes to continuous improvement initiatives. Daily tasks include maintaining IT communication policies, managing SharePoint content, generating reports, and coordinating procurement activities.

As a Principal Project Engineer, you will design and commission biopharmaceutical process equipment while providing engineering support for existing processes. Responsibilities include managing projects, preparing diagrams, supporting QA Validation, supervising contractors, and maintaining compliance with regulations.

The Associate Director of Project Engineering will lead the engineering team in designing and installing biopharmaceutical process equipment, ensuring project compliance, providing engineering support, and mentoring staff. The role involves managing projects and improving processes, while maintaining regulatory compliance and driving team performance.

The Reimbursement Business Manager will develop and execute account plans to enhance reimbursement confidence, educate physician offices on coding and coverage of Regeneron products, and resolve reimbursement issues. This role involves establishing relationships with healthcare professionals, managing product concerns, and ensuring patient access to care through proactive communication and planning.

The First Line Sales Manager at Regeneron will lead and coach a team of Sales Specialists, ensuring performance goals are met while managing resources and budgets. They will facilitate onboarding, provide feedback, and oversee advocacy development to achieve commercial objectives in the pharmaceutical industry.

The Principal Compliance Specialist ensures adherence to cGMP standards within the Engineering & Automation Department, guiding documentation processes, conducting evaluations, and coordinating audits and inspections to maintain regulatory compliance.

As a Product Specialist in Immunology sales for Regeneron, you will achieve brand sales objectives, develop territory business plans, manage budgets, utilize data sources for strategic planning, perform administrative duties, and collaborate with alliance partners, all while upholding regulatory compliance and delivering value to customers.

The Manager of Contract Operations and Customer Pricing oversees chargeback processes, manages a team, ensures accurate rebate processing, resolves data discrepancies, and communicates pricing changes to stakeholders. The role requires innovation and collaboration across departments to drive operational efficiency and support GPO programs.

The Associate Director, GPS Standards & Training, is responsible for developing, implementing, and maintaining SOPs and policies for pharmacovigilance within the GPS department. They will ensure compliance with global regulatory requirements while leading process improvements and managing quality events.

The Scientist in Protein Purification will support the purification and biochemical characterization of protein reagents, conduct protein purification and characterization, and perform laboratory testing and analysis of protein results. This role requires expertise in handling protein biochemistry, including various chromatography techniques and data documentation.