The MDR Specialist will evaluate product complaints, assess regulatory reporting requirements, and prepare Medical Device Reports (MDRs). They will also conduct investigations and collaborate with cross-functional teams to ensure compliance with quality system standards.
The Project Manager will oversee multiple drug discovery programs by maintaining integrated project plans, timelines, and trackers. They will lead program team meetings, manage cross-functional collaboration, and proactively identify risks to ensure project milestones are met.
Lead client software implementations from planning through configuration, validation, go-live, and transition to ongoing support, serving as the primary client contact. Manage project scope, schedules, budgets, risks, documentation, and cross-functional teams while delivering training and maintaining client satisfaction.
The UI/UX Designer will collaborate with stakeholders and developers to translate requirements into wireframes, prototypes, and visual designs for web and mobile applications. They are responsible for defining product functionality, creating user stories, and ensuring optimal user-system interaction through feedback loops.
Own the roadmap and delivery of one or more product feature areas, from customer discovery and business case development through release and post-launch measurement. Coordinate with engineering, design, QA, leadership, and customer-facing teams to prioritize work, manage delivery trade-offs, support launches, and communicate product direction.
Develop commissioning and qualification protocols for utilities and equipment using KNEAT platforms within the life science industry. Collaborate with cross-functional teams to assess risks and generate comprehensive validation documentation.
