The Senior Director Global Procurement will lead Strategic Sourcing and Procurement for Regeneron's international markets, driving key decisions to optimize global expansion. Responsibilities include leading cross-organizational projects, developing strategic plans, managing supplier relationships, and fostering effective team culture. The role requires collaboration with senior leaders to meet local market objectives while leveraging global capabilities.

The Director of IT Quality Assurance and Compliance leads a team focused on ensuring regulatory compliance across IT systems in the biopharmaceutical sector. Responsibilities include collaboration with QA teams, oversight of audits, risk analysis, training, policy enforcement, and fostering continuous improvement within the organization.

The Scientist will develop and apply computational methods for analyzing multi-omics datasets and collaborate with clinical teams to support therapeutic advancements. Responsibilities include building computational platforms and models, data processing, and visualization across various stages of therapy development.

The Quality Control Technical Resource Specialist supports QC lifecycle management by providing scientific expertise in assay development, validation, and investigation. Responsibilities include method performance monitoring, coordination with regulatory and external partners, drafting testing procedures, and training QC staff to maintain high quality standards in a fast-paced environment.

The Manager of Process and Procedures Operations ensures quality review of procedural documentation and system metadata. Responsibilities include managing workflows for quality improvements, preparing impact assessments, supporting inspection management, and negotiating complex situations. The role requires critical thinking and the ability to manage multiple priorities effectively.

The QC Analyst will conduct a variety of analytical chemistry tests to ensure compliance within a cGMP environment. Responsibilities include data gathering, reviewing test results, maintaining laboratory supplies, writing SOPs, calibrating instruments, and developing new analytical methods.

As a Lead Site Reliability Engineer, you will manage AWS platforms, implement and oversee cloud solutions, ensure security compliance, and develop automation scripts. You'll work with stakeholders to maintain system health, monitor performance, and provide operational support.

The Associate Manager will oversee payroll operations, assist in system implementations, manage day-to-day payroll processes, ensure compliance with regulations, and collaborate with multiple departments. Responsibilities include preparing documentation, training staff, resolving system issues, and handling payroll-related financial tasks at month-end and quarter-end.

The Specialist, Global Procurement – Supplier Quality Compliance is responsible for ensuring cGMP compliance in procurement operations. Key activities include maintaining compliance documents, managing supplier audits, coordinating with cross-functional teams, and supporting quality initiatives. The role involves proactive issue resolution and engaging stakeholders for effective supplier management.

As a Fill/Finish Operator at Regeneron, you will support the aseptic filling manufacturing processes for biopharmaceuticals. Responsibilities include operating automated equipment, ensuring stock levels, performing cleaning activities, assisting in routine and non-routine sampling, and documenting adherence to cGMP standards. You will work both individually and as part of a team, handling complex processes and continuous training.

Manage a team overseeing the maintenance and development of Regeneron's IOPS IT applications, primarily focusing on Oracle systems. Responsibilities include user support, team management, operational rigor, project completion, and ensuring regulatory compliance while contributing to the strategic vision for applications.

The Employee Listening Program Manager leads the organization's employee listening program, focusing on workforce lifecycle surveys and data analysis to provide actionable insights. Responsibilities include managing surveys, designing methodologies, visualizing data, and collaborating with various departments to enhance the listening program while ensuring compliance with data privacy and security standards.

The Senior Specialist, Global Procurement – R&D supports strategic sourcing initiatives by developing RFIs, RFQs, and RFPs, participating in supplier selection, negotiating contracts, and monitoring supplier performance. This role involves market analysis, compliance monitoring, and managing supplier relationships to ensure efficiency and compliance within procurement activities.

The Associate Director will develop and execute Category Management strategies within HR, handle supplier relationships, analyze proposals, negotiate contracts, and ensure compliance with procurement policies while optimizing cost effectiveness.

The Principal Quantitative Pharmacologist designs and conducts quantitative analyses to support program development strategies. Responsibilities include communicating results, authoring regulatory documentation, and preparing study reports. The role involves applying advanced pharmacokinetics, regulatory experience, and mentoring PMx staff.

The Director of IT Operations ensures reliable IT infrastructure operations in a GxP environment. Responsibilities include supervising IT staff, managing technology solutions, collaborating with corporate IT, ensuring compliance with standards, and overseeing vendor services. This role also involves defining IT policies, providing training, and improving the IT infrastructure.

The Executive Director Quality Control leads the Quality Control activities in pharmaceutical manufacturing, ensuring compliance with regulations and conducting various testing and investigations. They provide strategic guidance, support operational objectives, and collaborate with other departments to uphold quality standards.

The Senior Internal Auditor executes the annual risk-based audit plan, reviews processes and functions, and conducts audits in compliance with internal policies. They identify weaknesses and recommend operational enhancements, while preparing drafts for senior management and contributing to SOX 404 compliance.

The Associate Director, GPS Standards & Training is responsible for establishing and maintaining regulatory procedures and policies in the GPS department, ensuring training compliance, leading quality enhancements, managing quality events, and ensuring inspection readiness for audits. This role involves collaboration with various stakeholders and requires strong organizational skills and experience in pharmacovigilance.

The Director of Global Procurement Compliance leads a team to ensure cGMP compliance in procurement operations. This role involves managing supplier audits, overseeing compliance strategies, and collaborating with stakeholders to enhance procurement processes. The director will also track quality system deliverables and support regulatory inspections.