Search the 116 jobs at Regeneron

Sales Specialists engage key professionals and customers, managing and growing key accounts in the mid-South territory. Responsibilities include developing account plans, collaborating with partners, and ensuring compliance with regulations. The role involves demonstrating strong sales performance and connecting work to brand strategy while prioritizing patient access.

The Sr QA Project Specialist leads cross-functional projects and develops project timelines within the Change Control Business Process Management team in the pharmaceutical industry. Key responsibilities include managing project priorities, collaborating with subject matter experts, engaging in timely execution, and maintaining project alignment through effective communication.

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 Manager, Quality Compliance will manage a team of Compliance Specialists overseeing Supplier Corrective Action Requests and quality assurance processes. Responsibilities include mentoring, ensuring compliance with QMS systems, supporting audits, driving process improvements, and managing quality assurance initiatives.

The Global Procurement Specialist supports Category Management by anticipating supply needs and specifications for Raw Materials. Responsibilities include assisting the Category Manager, managing vendor relationships, ensuring accountability, driving cost savings, and supporting compliance with regulations. The role involves project management, contract management, and utilizing data for informed decision-making.

The Associate Manager/Manager QA will lead the QA team, ensuring compliance with quality policies in drug substance manufacturing, reviewing critical documentation, coordinating resources, monitoring compliance, participating in audits, and driving improvements in QA processes. The role also involves managing projects focused on digital transformation and collaborating with cross-functional teams.

The Process & Procedures Coordinator supports operational activities by managing project files, assisting with project plans, maintaining stakeholder communications, and organizing onboarding processes. The role requires effective project management in a regulated global environment and proficiency in Microsoft Office.

The Manager, Market Analytics & Reporting will lead analytics projects, manage customer data analysis, support sales & marketing efforts, and generate reports for senior management to enhance business intelligence and operational effectiveness.

The Archives Specialist will manage the transfer and compliance of records, maintain record inventories, support legal research for retention values, and collaborate with IT to enhance recordkeeping systems. The role involves ensuring adherence to GLP requirements and supporting inspection readiness.

The Automation Engineer will design, develop, and implement improvements for automated equipment, troubleshoot manufacturing deviations, create engineering documents, and support process control systems in a biopharmaceutical manufacturing setting.

The Manager is responsible for maintaining the Global Development Quality Management System, overseeing quality events, and implementing process improvements. They engage with stakeholders to ensure regulatory compliance and manage quality-related metrics, governance activities, and training on quality standards.

The Manager, Statistical Programming leads programming support for clinical studies, ensuring data is processed according to specifications and standards. Responsibilities include coding, documentation, maintaining quality control, and collaborating in multidisciplinary teams for analysis and reporting up to product launch.

The Senior Manager Market Access oversees HTA submissions, pricing implementation, negotiation, and tender strategy in the Benelux and Nordic Markets. They coordinate cross-functional strategies with global and affiliate teams, develop pricing strategies with the Affiliate Commercial team, support market access plans, and assess new product launches.

The Associate Manager MES Operations oversees the implementation and daily functioning of the Manufacturing Execution System at Regeneron. Responsibilities include ensuring system alignment with business needs, collaborating with various functional groups, developing strong business relationships, ensuring compliance, and providing support for user testing and training.

The Associate Director for QC Technical Resources will oversee method validation and transfer processes for incoming components and drug products. Responsibilities include ensuring compliance with regulations, providing analytical support across departments, managing QC Analysts, and overseeing investigations of atypical results while reporting progress to management.

The Lead Site Reliability Engineer will manage the AWS platform and implement scalable cloud solutions. Responsibilities include serverless and containerized applications management, infrastructure as code development, system performance monitoring, and operational support. Close collaboration with various stakeholders to enhance cloud services and address any technical incidents is essential.

The Associate Manager, Payroll Operations and Analytics will oversee payroll processes and system implementations using Oracle Payroll and OTL. Responsibilities include analyzing payroll data, ensuring compliance, documenting procedures, managing payroll related projects, collaborating with various departments, and training staff. The role also involves tax processing and reconciliation tasks.

The Quality Assurance Specialist will support product and raw material disposition by ensuring compliance with quality policies and procedures, participating in investigations, advising on QA practices, and reviewing batch records. This role requires collaboration with various departments to maintain quality standards and promote continuous improvement.

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.