Jobs at Regeneron Pharmaceuticals, Inc in Troy, NY

Project Specialist-Technology Transfer role at Regeneron, providing project management support for the internal/external technology transfer of biopharmaceutical drug substance manufacturing processes...

The External Manufacturing Specialist coordinates all aspects of contract manufacturing operations, ensuring timely completion of operations/documentation and monitoring cGMP compliance...

The Change Control Specialist (Manufacturing) is responsible for developing strategic plans related to change control and implementing corrective actions to support manufacturing operations. They will...

The QC Technical Resources Specialist - Bioassay position at Regeneron is responsible for managing cell-based and binding assays used in Quality Control testing. This role offers the opportunity for s...

The Senior Inventory Management Analyst - Metrics & Reporting is responsible for executing data analytics, designing reports, and forecasting to improve overall supply chain processes. They also ensur...

Senior Project Specialist - Manufacturing Planning

The Sr QA Documentation Specialist (Archives) position provides support to the site(s) related to documentation system and ancillary support systems, coordinates with other sites to ensure global harm...

The Associate Director, Information & Records Management is responsible for leading all aspects of the records management program, ensuring compliance with regulatory and legal requirements. They will...

Manager responsible for overseeing quality review, approval, and management of investigations and corrective actions in the pharmaceutical industry.

The Quality Compliance Specialist ensures quality and compliance to cGMPs, internal, external, and international requirements with respect to change control activities. This role works within the QA C...

Reviewing design and development paperwork and records for compliance to internal procedures and regulations.

Manager, Information and Records Management position responsible for overseeing operations of the Information & Records Management group and providing global support...

The Associate Manager- Process Sciences (Cell Banking) role at Regeneron involves leading and coordinating daily operations of the Process Sciences Department, conducting laboratory experiments, analy...

The Director of CMC Industry and Regulatory Intelligence is responsible for monitoring and influencing global regulatory and industry trends, ensuring compliance and driving excellence in chemistry ma...

Associate Director- QC Microbiology (Fill Finish) responsible for managing QC laboratories/sampling for assigned functional areas, including Raw Materials, Microbiology, Chemistry, Biochemistry, Biolo...

The Sr Director of GMP Compliance & Inspections will ensure continuous GMP compliance and build inspection readiness capability across the organization. They will lead evaluations of GMP compliance, m...

The Associate Director of Regulatory Affairs, CMC will provide strategic management and leadership to support the Regeneron portfolio of products assigned, with a focus on gene therapy products. They...

Associate Manager QC (Quality Control) responsible for overseeing a personnel team supporting a 24/7 operation, driving improvements in KPIs, metrics, and team performance, and ensuring compliance wit...