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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 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 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.
The Scientist will support the development of cell and gene therapies, focusing on mammalian cell culture, T cell preparation, retroviral vector design, and various assays and molecular biology techniques. You will work independently and collaboratively in a fast-paced environment, utilizing skills in flow cytometry and cell manipulation, among others, to drive innovation in bispecifics.
The Staff CMC Regulatory Sciences Specialist oversees CMC aspects of global submissions, focusing on regulatory strategies and the preparation of submissions for non-US/EU markets. The role involves developing processes, managing cross-functional teams, providing regulatory guidance, and monitoring trends in non-US/EU markets.
The Process Development Associate II in Purification Development is responsible for developing purification processes, documenting experiments, maintaining laboratory instruments, and supporting technology transfers. You will also engage with team members to improve efficiency and safety, present findings in meetings, and assist in training peers and interns.
As a Process Development Associate II in Analytics, you will perform analytical experiments to support biopharmaceutical manufacturing process development. Your role involves high throughput analysis, statistical evaluations of assay performance, communication with project teams, and developing new analytical assays within a collaborative environment.
As a Process Development Associate II at Regeneron, you will focus on developing bioreactor processes for cGMP manufacturing, cultivating mammalian cells, and analyzing data for process understanding. You'll also participate in technology transfer and produce reagents for R&D.
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.
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