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The Senior Workplace Coordinator manages workplace strategy projects, providing support for planning, procurement, and installation of lab equipment and furniture. Responsibilities include coordinating day-to-day activities, maintaining budgets, facilitating communication between departments, and managing vendor relations to ensure efficient project execution with minimal disruption.
As a Senior Automation Engineer, you will design and implement software/hardware improvements, provide technical support for manufacturing and quality control, troubleshoot automation system deviations, and develop necessary documentation for equipment. You will work in a regulated environment to improve biopharmaceutical manufacturing processes.
The Principal Project Manager - Engineering designs and specifies biopharmaceutical process equipment, manages projects related to these systems, prepares engineering documentation, and supports QA/Validation departments. This role includes overseeing installation, supporting investigations, implementing corrective actions, and may require domestic and international travel.
The Innovation Protection Specialist is responsible for managing medical device development portfolios, focusing on innovation protection strategies, due diligence, and legal agreements. They collaborate with internal teams to support medical device R&D, provide metrics on intellectual property matters, and educate colleagues on compliance processes.
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 Staff Accountant provides accounting analysis and reconciliation support for areas such as labor reporting, fixed assets, and intercompany activities at Regeneron. Responsibilities include assessing financial impacts, supporting inventory standard costs, collaborating with other departments, and applying GAAP for accounting tasks and reconciliations. Continuous improvement ideas and audit assistance are also part of the role.
The Associate Manager, Research Program Management will oversee the quality and accessibility of scientific project data, ensure data accuracy, manage discovery portfolios, and provide insights for decision-making. This role will also involve improving data management processes and mentoring others in the use of PPM systems and tools.
The Sr. Manager Development Program Management leads operational direction for development programs in the drug development industry, managing multiple projects through their lifecycle and collaborating with cross-functional teams. Responsibilities include planning, budget oversight, risk mitigation, and facilitating communication across stakeholders to drive program success from preclinical to commercialization.
The Scientist in Auditory Sciences will conduct basic research on deafness and hearing impairment, performing experiments with animal models, analyzing data, and working collaboratively with a team to advance understanding in the field. Responsibilities include maintaining cultures, characterizing hearing models, and executing experiments involving surgical techniques.
The Archives Specialist will manage the transfer and compliance of records, maintain record inventories, support legal research for retention values, and collaborate with IT to enhance recordkeeping systems. The role involves ensuring adherence to GLP requirements and supporting inspection readiness.
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