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Seeking a motivated Scientist to join Human Antibody Isolation Team, contributing to the identification of antibodies for treating various diseases. Responsibilities include isolating monoclonal antibodies, developing new isolation technologies, conducting experiments, and maintaining records. Requires a PhD with 0-3 years postdoc experience or BS/MS with 4-8 years in Immunology, Cell Biology, or Molecular Biology. Hands-on experience in cell culture, PBMC isolation, flow cytometry, and molecular biology techniques is necessary. Comfort with handling mice is expected.

Responsible for providing technical support on the manufacturing process, implementation of large scale commercial manufacturing production program, and technical transfer of processes. Key duties include liaising with process science/technology transfer teams, providing technical input into manufacturing records, resolving process problems, supporting manufacturing personnel, and implementing process improvements. Requires BS/BA/BEng in Life Sciences or related field and 2+ years of relevant cGMP Manufacturing/Engineering/Scientific experience in a Drug Substance Biotech facility.

Seeking a Senior Manager Product Management at Regeneron Pharmaceuticals in Sleepy Hollow, NY. Responsibilities include providing technical design and execution support for global sales technology, managing CRM strategy, leading advancements, and collaborating with cross-functional teams. Requires a Bachelor's degree in Computer Science or related field and 8 years of IT technology platform experience. Must have expertise in Veeva, Salesforce.com, data architecture, integration architecture, and product development lifecycle.

The Senior Manager, Global Development Quality Management (GVP) at Regeneron is responsible for leading quality and compliance activities within the global pharmacovigilance system. This role involves building strategic partnerships, managing inspection readiness, and identifying systemic quality issues for remediation. The ideal candidate should be proactive, self-motivated, and experienced in GVP with a background in post-marketing and clinical trial safety.

The Manager of Supply Logistics manages the third-party warehousing operation to ensure compliance and support business objectives. Responsibilities include overseeing 3PL performance, developing operational solutions, and collaborating with cross-functional teams. The role requires strong leadership, problem-solving, and communication skills. Ideal for candidates with extensive experience in Supply Chain and Logistics.

The Senior Manager, Global Development Quality Management (GCP) is responsible for providing guidance and leadership for all aspects of quality and compliance within Global Development Quality systems. This role involves engaging with stakeholders, leading risk-based quality management activities, and ensuring GCP compliance on clinical trials.

Regeneron is seeking a Data Review Associate to ensure data integrity in documentation related to quality events and manufacturing of pharmaceutical products. Responsibilities include data integrity reviews, data gathering, verification, and statistical analysis. Candidates should have a bachelor's degree in life sciences, mathematics/statistics, or related field. Positions available for candidates with 0-2 years of related experience.