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The Senior Quality Compliance Specialist manages quality assurance activities related to partner change notifications. Responsibilities include facilitating external partner meetings, developing change control processes, mentoring staff, ensuring compliance with regulations, and maintaining effective relationships across departments. They are also involved in audits and inspections, and advocating for continuous improvement initiatives.
The role focuses on isolating and developing monoclonal antibodies for treating diseases, involving techniques like flow cytometry and ELISA. Responsibilities include laboratory work, data analysis, and collaborating with teams to innovate antibody technologies.
The Technical Lead for Application Development at Regeneron Genetics Center will provide technical leadership, develop solutions across the tech stack, engage with internal clients, manage application timelines, coordinate with DevOps on AWS infrastructure, and ensure alignment with architecture guidelines, all while fostering operational excellence in a fast-paced environment.
The Manager of Statistical Genetics will lead research efforts in Statistical Genetics and Genetic Epidemiology, focusing on large scale genetic variation analyses. Responsibilities include performing GWAS, analyzing exome sequencing data, integrating genetic results with human diseases, and developing statistical methods. The role involves collaboration and communication with a diverse team to drive genetic discovery.
The Associate Workplace Planner supports the workplace planning team by managing furniture for capital projects, overseeing wayfinding and signage, contributing to special projects, attending capital meetings, and collaborating internally. A focus on planning principles and strong communication skills is required.
The Senior GMP Quality Auditor will plan, coordinate, and execute audits, focusing on compliance with GMP and other relevant regulations. Responsibilities include conducting supplier audits, maintaining training requirements, preparing audit reports, and developing corrective and preventive actions, while ensuring compliance with both local and international standards.
The GMP Quality Auditor is responsible for planning and conducting audits in accordance with GxP regulations, maintaining audit documentation, collaborating with stakeholders, and ensuring compliance with quality standards. They will supervise trends in regulatory agency findings and prepare comprehensive audit reports while providing mentorship for corrective actions.
The Sr. Bioinformatics Data Analyst will lead and contribute to the software lifecycle of Scientific Data Applications, collaborating with scientists to enhance data models and accessibility. Responsibilities include designing scalable data solutions, analyzing data issues, unifying master data for quality improvement, and mentoring team members on best practices in data solutions and architecture.
The Principal Statistical Programmer will lead and support programming activities for clinical studies, ensuring high-quality programming deliverables. Responsibilities include programming support, documentation development, and assisting regulatory submissions. The role requires analytical proficiency and collaboration with internal teams.
The Sr. Application Developer will develop and maintain applications for analyzing genetic data, modernize existing applications, implement user-requested features, and provide support to users. The role requires collaboration with a diverse team and a strong interest in computational genomics.
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