Responsibilities: Provide leadership, strategic planning, direction and implementation of clinical systems for data collection which may include vendor selection, budgeting, resource planning, vendor oversight, EDC build and study timelin...
Responsibilities: The Combination and Medical Device Products team is developing a replacement infusion system for Parkinson's Disease therapy. We are in the design transfer and launch preparation phase of the project and are looking for ...
Responsibilities: Design, build, document, and maintain custom state of the art RNAseq and other OMICs data-analysis pipelines and front-end tools for a large user base. Detect and resolve software bugs and performance issues. Provide on...
Job Description: We are seeking a skilled and proactive Business Analyst to support the implementation of Veeva Vault RIM Submissions, with a specific focus on authoring capabilities for Life Sciences regulatory submission content managem...
Responsibilities: The Regulatory Affairs Level III (Senior Specialist) position is responsible for global product registrations and ensuring regulatory compliance in the design, manufacturing, and sales of medical devices (including Class...
Job Description: This role provides hands-on support for Syncade MES and DeltaV automation systems within a GMP-regulated manufacturing environment. The specialist will troubleshoot systems, support production floor activities, perform tes...
Job Description: Provides quality oversight to the clinical trial delivery quality systems, promoting operational and compliance excellence, quality risk management and knowledge management. Maintains a state of control by implementing e...
Job Description: The Quality Engineer I plays a key role in maintaining product quality, compliance, and process control for medical device manufacturing. This position ensures adherence to regulatory standards, drives continuous improveme...
Job Description: The Manufacturing Associate is responsible for executing manufacturing operations for therapeutic protein (API) production under cGMP conditions. This includes operating equipment, following SOPs, performing basic lab task...
Job Description: Role is responsible for designing, planning, and executing large scale data analysis, and algorithm development to identify gaps in the care continuum and to measure impact using RWD. This work highlights the value of ut...