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Lead development and deployment of data science, machine learning, and AI solutions across commercial teams. Manage projects, build predictive models and prototypes in Python, query data with SQL, collaborate cross-functionally, present results, ensure regulatory compliance, and support vial-filling manufacturing operations.

The Product Engineer supports production engineering in testing methods, device issues, equipment design, and ensures compliance with quality standards in manufacturing operations.

Manage DeltaV automation upgrade projects in regulated environments, coordinating engineering, IT, and vendors while ensuring compliance and risk mitigation.

The job involves overseeing capital projects, ensuring compliance with regulations, developing project documentation, scheduling, and managing resources while promoting a productive work environment.

Coordinate capital projects in a regulated (pharmaceutical/medical device) environment: support planning and scheduling, contractor coordination, risk assessments, document tracking, status reporting, and GMP/GDP compliance, working with project managers and cross-functional teams to deliver projects on time and on budget.

The Sr. Project Manager will oversee project development and implementation in Capital Projects, managing budgets and cross-functional teams for successful outcomes.

Lead technical strategy and delivery for robotics and ASRS across sites: define architectures, establish standards, integrate PLC/HMI/safety/robotics with WMS/WES/WCS/EMS, oversee OT/IT decisions, manage FAT/SAT/commissioning, drive root-cause resolution, ensure functional safety, and supervise OEMs/integrators through handover and sustainment.

The Senior Supplier Quality Engineer will oversee supplier quality assurance, manage approvals, audits, and ensure compliance with manufacturing and quality standards in the medical devices industry.

The C&Q Lead will manage overall commissioning and qualification planning, coordinate multidisciplinary meetings, ensure compliance, handle change control, and oversee documentation related to CQV activities in the pharmaceutical industry.

This role involves supporting quality assurance in manufacturing, including compliance, systems validation, and IT systems integration, requiring communication and teamwork.