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Design, develop, and optimize sophisticated biopharmaceutical manufacturing processes by implementing software/hardware improvements and providing technical support for automation systems. Troubleshoot and investigate manufacturing deviations and anomalies while adhering to cGMP guidelines. Support manufacturing and engineering projects and ensure compliance with system specifications and testing protocols.
Responsible for maintaining site compliance of operations including manufacturing, quality systems, quality control, and facilities maintenance. Participates in continuous improvement initiatives, interprets compliance requirements, and supports investigations of deviations related to quality. Requires a Bachelor's degree and 2+ years of relevant experience.
Collaborate with cross-functional teams to provide scientific expertise in study design, new products, and change management. Manage analytical projects, interpret data, evaluate new materials for GMP production, lead meetings, and review technical documents. Stay updated on industry guidelines for extractables and leachables. Requires BA/BS in chemistry, biology, or related field.
Design, develop, and implement software/hardware improvements to automated equipment, troubleshoot manufacturing deviations, support small projects, and author system specifications. BS in Engineering or related field required with 2+ years of experience for Automation Engineer role.
The Senior IT Applications Analyst is responsible for the configuration, validation, implementation, maintenance, and ongoing support of various IT applications and systems. They will lead efforts as the Subject Matter Expert on system configuration, technical change controls, and audit activities. Responsibilities include translating business and technical requirements, providing architecture designs, collaborating with architectural leadership, and supporting solution development and integrations.
Responsible for delivering complex and strategic IT projects across Applications and Infrastructure for IOPS. Manage project delivery within budget, scope, quality, and time requirements. Communicate with team members and stakeholders to ensure project success. In-depth knowledge of Project Management, SDLC, PM Tools and Processes, Enterprise systems, and Life Sciences environment required.
The Principal Quality Compliance Specialist at Regeneron is responsible for ensuring quality and compliance to cGMPs, internal, external, and international requirements with respect to change control activities. This role involves partnering with the Quality Assurance team, facilitating process improvements, developing tools for consistent communication, interpreting compliance requirements, and more.
Senior IT Applications Analyst specializing in Kinaxis RapidResponse for supply chain planning solutions delivery. Responsibilities include requirements analysis, customization, testing, training, documentation, and communication. Experience in implementing Kinaxis Advanced Planning tools and managing full lifecycle supply chain planning projects.
The Senior Manager IT Operations supports Executive Technology, ensuring reliable operation of the IT and AV infrastructure for senior leadership. Responsibilities include daily support for senior leadership events, oversight of A/V equipment and conferencing services, project management, troubleshooting technical issues, planning and provisioning for large events, and maintaining knowledge objects and work instructions.
Join Regeneron's new immunology sales team in Italy as a Sales Specialist. Achieve brand sales objectives, develop and implement territory business plans, work within regulatory guidelines, and collaborate with alliance partners. Requires superior customer engagement skills, technical competence, and written and verbal communication abilities. Bachelor's degree and 5 years of sales experience in the pharmaceutical industry required, with previous experience in the biologic market highly desirable.
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