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The Field Application Scientist will engage scientifically with customers in pre/post-sales by providing consultations, product demonstrations, and training. They will develop expertise in instrumentation, maintain knowledge of assays and workflows, and relay customer feedback to product management. A strong background in cell-based assays and data analysis software is required, and the role involves significant travel.

Serve as a concierge for enterprise services, primarily assisting pharmaceutical companies with operational requests, including equipment inspection and repair services. Coordinate schedules for engineer visits and manage related tasks in a timely and honest manner.

This role involves comprehensive field service for GC and GC/MS chemical analysis equipment, including installation, operational guidance, validation, diagnostics, repairs, and promoting sales of related products. Candidates will work primarily in western Japan, focusing on customer interactions and technical support.

As a Field Service Engineer, you will support customers by installing, maintaining, and troubleshooting Pathology systems solutions, ensuring high levels of customer service. You will work with a diverse array of products, providing insights and technical support to prevent equipment issues and optimize product performance.

As a Product Specialist, you will leverage technical knowledge to sell Agilent Mass Spectrometry systems and workflows, build customer relationships, drive opportunities through the sales cycle, and provide market feedback to R&D. You will participate in conferences, negotiate complex sales, and communicate with internal teams to enhance customer satisfaction and achieve sales goals.

The Engineering Manager will lead a team in capital expansion projects, supporting design, construction, and qualification activities in an API-Biopharma manufacturing environment. Responsibilities include managing project schedules and budgets, supporting technical transfers, environmental health and safety activities, validation processes, and quality assurance functions, enabling the growth of oligonucleotide manufacturing capabilities.

The Global Quality and Regulatory Affairs Field Action Specialist is responsible for managing field action activities, recalls, and correction processes for medical and non-medical products. This includes coordination of notifications, health hazard evaluations, and regulatory interactions. The role involves monitoring product quality issues, executing field actions, and ensuring regulatory compliance. The position also involves maintaining and developing quality management system processes for field actions and communicating with various stakeholders and global health authorities.