The Success Manager is a newly created position in the Fujifilm Business Innovation Division (BID) that will oversee the experience for customers and sales staff at the Graphic Innovation Hub (GIH). Located in our North America headquarters, the GIH is a 24,000 sq/ft innovation and technology center filled with Fujifilm’s industry leading solutions for inkjet, toner, wide format and packaging print. Every day we host customers from across North America so they see, learn, and experience how Fujifilm innovations can transform their business.

As the Success Manager, you will work together with the GIH Technical Manager, the product demonstration team, marketing team, and the sales team, to plan and execute a truly exceptional experience for customers. Product demonstrations are a key part of the buying journey and sales experience for customers. Our demo center hosts more than 150 demos per year ranging from 1:1 in person tours to large scale VIP events.

The purpose of this role is to provide customer support of Fujifilm ES equipment in the Endoscopy department and/or specified departments by managing all relevant equipment, providing basic trouble shooting, and training for proper care and handling of our equipment. This role provides onsite, hands-on client support for Fujifilm Endoscopy’s entire product catalog. This role provides education and training to Company personnel and customers. This position reports directly to the Regional Sales Manager or Zone Sales Director and is the primary sales support resource for the Company and its sales team.

The purpose of this role is to provide customer support of Fujifilm ES equipment in the Endoscopy department and/or specified departments by managing all relevant equipment, providing basic trouble shooting, and training for proper care and handling of our equipment. This role provides onsite, hands-on client support for Fujifilm Endoscopy’s entire product catalog. This role provides education and training to Company personnel and customers. This position reports directly to the Regional Sales Manager or Zone Sales Director and is the primary sales support resource for the Company and its sales team.

The Warehouse Assistant will be responsible for all Warehouse daily activities related to Receiving, Put away, Returns, Picking, Shipping, Housekeeping and all SAP transactions to close and directly reporting to the Warehouse Manager. The Warehouse Assistant will report all issues related to the daily activities to the Warehouse Floor Supervisor.

The Manager, CSV will be responsible for management, scheduling, and oversight of all GxP-Regulated Computerized Systems at all applicable points of the computerized system lifecycle, ensuring compliance with regulatory requirements, Computer Systems Validation (CSV) and Lifecycle procedures with Data Integrity requirements at each of our 4 Manufacturing Buildings (NCTM, TBF-100, FBF-200, FBF-300). The Validation Manager will be responsible for updating the corresponding manufacturing building’s Systems Master List, Requalification Schedule, and management of Validation Engineers/Specialists for day-to-day validation activities. They will provide oversight of validation activities, lead the development and approval of validation documentation, risk assessments, work with project teams to determine which elements should be validated, and conduct impact assessments of proposed changes to computerized systems.

Manufacturing Associate (1st Shift, Transducers) - Bothell, WA

This position is responsible for performing a variety of tasks associated with manufacturing diagnostic ultrasound transducers.  Specific tasks may include some of the following:

The Clinical Specialist (ARDMS Certification Required) - Boston, MA position is responsible for understanding and addressing the clinical needs of customers within an assigned territory.  The Clinical Specialists partner with Territory Managers to demo FUJIFILM Sonosite products, close deals, and ensure ongoing positive customer experience.  After the sale, this role owns client relationships and works to encourage customer adoption and use of FUJIFILM Sonosite products.

Note: This position is open to candidates who currently reside in the Boston area as this would be a central location relative to the territory's business.

The Manager of Environment, Health & Safety (EHS) will lead EHS and sustainability programs at the New Castle facility, driving improved performance through implementing EHS programs, ensuring KPIs are met and investigating all incidents /near miss. The position will also be responsible to ensure all environmental and compliance requirements for the facility are met. The position is also responsible to lead the safety committee and delivering all relevant training for the employees. This site is ISO 14000 certified.

The Quality Control Chemist III, with limited supervision, will be responsible for participating in the Technology Transfer of established methods into the FUJIFILM Biotechnologies Quality Control Laboratory.  Following Tech-Transfer Activities, the candidate will be responsible for performing in-process, release and stability testing using the established analytical methods.

FUJIFILM Electronic Materials, U.S.A., Inc., is a global leader in chemical solutions which enable the semiconductor industry and the digital universe. We have an exciting opportunity for a Maintenance Technician I at our Hollister, CA facility!

The Role

As a Maintenance Technician I, you will be responsible for performing mechanical maintenance and installations for manufacturing, cleanroom, lab, and facilities. These activities include items such as: repair and installation of plant piping systems, repair and installation of packaging/conveyor systems, general utility repairs.

This person will also be involved in day-to-day maintenance activities to include completion of work orders, electrical motor change outs, and preventative maintenance tasks. Hours worked may vary based on business need (i.e. to maintain production schedule, emergencies, etc.).

The Senior Technical Clinical Consultant, Cardiology shall be responsible for all aspects of the reporting design and build, configuration, workflow, measurement/data mapping for project and or post go-live support cases in compliance with the company’s quality procedures.

The Manufacturing Technician II works directly with a range of technologies. Dependent upon assignment, the range of technologies may include any of the following:

Position Description - Manufacturing Quality Engineer II for FUJIFILM Dimatix, Inc, Lebanon, NH.

Design, implement, and maintain quality assurance protocols and methods for processing materials into partially finished or finished products. Plan, implement, and manage compliance of manufacturing and production processes with internal and external safety, quality and regulatory standards requirements for worldwide distribution. Design methods and procedures for inspecting, testing and evaluating the precision and accuracy of production processes, production equipment and finished products. Performs analysis of reports and production data to identify trends and recommend updates or changes to quality standards and procedures. Review nonconformities and works with Supplier Quality Engineering to coordinate supplier corrective actions. Lead Internal Corrective Action Request (ICAR). Minimize product quality risk. Drive continuous improvement in product designs and manufacturing processes. Partner with key individuals to identify opportunities for continuous improvement through testing and analysis of manufacturing process data. Work with cross-functional teams to analyze and resolve any issues arising from Manufacturing Process, Engineering Review Board (ERB), or Material Review Board (MRB). Perform process statistical analysis. Manage multiple continuous improvement projects simultaneously. Implement statistical modeling using Minitab. Perform manufacturing-related data analysis and related distributions. Employ MRB and ERB reviews. Utilize manufacturing quality tools including FMEA, DFMEA, PFMEA, control plans, process verification/validation plans, Cpk, Cp, SPC, DOE, process data analysis, and DMAIC. Apply international quality system standards including ISO 9001.

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Good data is the key to the future success of the company, and this role is essential to ensuring our data is the best in the industry!  The Data Analyst is responsible for matching and cleaning customer data between disparate applications ensuring complete alignment to support automation projects.

The Data Operations Specialist (Temporary - 3 months) is responsible for maintaining and managing customer and item catalog data for FUJIFILM Sonosite and VisualSonics.

The I&C Engineer provides engineering support to field personnel in the performance of maintenance and operational tasks associated with instrumentation and automation systems and controls across the campus. The I&C Engineer provides support for the metrology department through evaluations of instrument deficiencies, test equipment issues and calibration strategies and methods. This role works directly with other Utility Engineers ensuring applicable safety and regulatory standards are maintained, identifies process improvements, and assists with troubleshooting equipment issues to maintain overall plant reliability. Additional responsibilities includes supporting deviation investigations and documentation for associated system deficiencies.

Utility Maintenance 2 will perform corrective maintenance, routine maintenance, and preventive maintenance on plant utilities equipment following Standard Operating Procedures (SOPs). Complete work orders, daily logs and forms following Good Manufacturing Practices (cGMP) documentation practices and quality standards in a Pharmaceutical Manufacturing plant. Utilities to include high-pressure steam boilers, process wastewater treatment, chillers, water purification systems (water softening and carbon bed filtration, reverse osmosis, deionization equipment, sanitary pumps, and associated equipment), compressed air and dryers, and chilled water

The Technician 2, Maintenance is responsible for the installation, maintenance, and repair of process related systems/equipment. Ensure these systems meet the stringent requirements of pharmaceutical manufacturing. Also responsible for conducting regular inspections and preventive maintenance on process related equipment to ensure equipment is operating efficiently with minimal downtime.

The Technician 3, Maintenance is responsible for the installation, maintenance, and repair of process related systems/equipment. Ensure these systems meet the stringent requirements of pharmaceutical manufacturing. Also responsible for conducting regular inspections and preventive maintenance on process related equipment to ensure equipment is operating efficiently with minimal downtime.