Here are our current job openings that match your search criteria. Please click on the job title for additional information or to apply to the opening.
If you are a current employee, please use this link to apply via our Internal Application Portal.
Use the form below to perform another search.
The Inbound Inspector is responsible for the inbound inspection for all endoscopes returned to the facility for service and/or repair. Performs initial inspection, defines the necessary repairs and lists the parts and components needed to complete the repair process. Works on all models of Loaner/Demo and Customer scopes.
This entry-level position is responsible for technical repair and final quality inspection on assigned Endoscopic units. This position is responsible for consistently meeting monthly repair targets while adhering to all safety policies and procedures.
As an upstream supervisor, you’ll lead and inspire a team of manufacturing associates, supporting the start up of a new large scale cell culture facility. The Upstream area includes: An inoculum lab, two seed reactor trains (each with 4 reactors of increasing size), four 20,000L production reactors, a harvest suite, media preparation, and parts prep area.
You and your team will work a 2-2-3, 12 hour shift schedule to support the ongoing activities in these areas.
You’ll start out leading a team in project phase supporting commissioning and qualification efforts in addition to helping prepare the facility to be operational ready. It’s an exciting opportunity to help build out processes and procedures in preparation of the first GMP run later this year.
*Relocation Assistance Available*
The Production Scheduler, Drug Product Finished Goods is responsible for creating, maintaining, and optimizing daily and long-term production schedules across drug product manufacturing, filling, inspection, and packaging operations. This role ensures timely product delivery and efficient use of resources while adhering to current Good Manufacturing Practices (cGMP). Acting as a central coordination point, the scheduler partners with other departments (e.g., Manufacturing, Planning, Quality, Supply Chain) to align material availability, equipment capacity, and staffing needs with the production plan.
We are hiring a Senior Counsel to be an integral part of the legal team providing support to the Medical Device businesses of FUJIFILM Healthcare Americas Corporation and FUJIFILM SonoSite, Inc., wholly-owned subsidiaries of FUJIFILM Holdings America Corporation (HLUS). The Senior Counsel, reporting to the Division General Counsel, Medical Devices, will be an experienced commercial transactions lawyer, responsible for working independently and collaboratively on legal issues affecting the Medical Device businesses to minimize risks of legal liability and ensure maximum legal rights of the company. The right candidate will be excited to join a growing company with a diverse portfolio of businesses. This attorney will be a senior legal resource and valued business partner for HLUS and its Medical Device businesses.
Please include cover letter and resume indicating your interest and expertise in this position.
Fujifilm Sonosite is seeking a Reliability Engineer to support R&D Systems Engineering developing Point-of-Care ultrasound medical devices in Bothell, Washington. As an individual contributor, you will support the entire lifecycle of ultrasound systems, including transducers and accessories. This position will be a champion and focal point on new product development teams using a Design for Reliability (DfR) approach starting early in the design process to ensure designs are robust to customer use, environmental stress, and service-life duration. The position will also support released products with failure rate analyses, reliability improvement projects, and safety risk assessments of field failure issues. You will work collaboratively within a technical cross-functional team to plan Design for Reliability efforts, including reliability analyses, HALT tests, reliability demonstration test programs, and engineering analyses. This position involves strong partnership with Hardware Engineering, Software Engineering, Program Management, Quality, Supplier Quality, and Manufacturing to lead, champion, and act as focal point for the reliability aspects of assigned projects.
The Project Manager 2 is responsible for collaborating with internal and external stakeholders, including but not limited to Environmental, Health & Safety(EHS), Maintenance, contractors, vendors, and clients. This role is responsible to handle administrative aspects of the project from start to completion, track and monitor the project status and milestones, and ensure projects meets all standards, timelines, and budgets.
POSITION SUMMARY:
Defines, develops and implements MES solutions based on technical requirements. Configures system settings and options; plans and executes unit, integration and acceptance testing of new MES software; creates specifications for MES and supporting systems to meet business requirements. Participates in cross-functional linked teams to design, architect and implement MES based solutions..
Knowledge: Developing professional expertise, applies company policies and procedures to resolve a variety of issues.
Job Complexity: Works on problems of moderate scope where analysis of situations or data requires a review of a variety of factors. Exercises judgment within defined procedures and practices to determine appropriate action. Builds productive internal/external working relationships.
Supervision: Normally receives general instructions on routine work, detailed instructions on new projects and assignments.
Experience: Typically requires a Bachelor’s degree and a minimum of 2 years of related experience; or an advanced degree without experience; or equivalent work experience.
POSITION SUMMARY:
Collaborates with content experts to analyze complex business problems to be solved with automated systems. Provides technical expertise in identifying, evaluating and developing systems and procedures that are cost effective and meet user requirements. Configures system settings and options; plans and executes unit, integration and acceptance testing; and creates specifications for systems to meet business requirements. Participates in cross-functional linked teams to address business or systems issues. May work with in conjunction with Professional Services to provide requirements and solutions to integrate or improve manufacturing systems
KNOWLEDGE : Learns to use professional concepts. Applies company policies and procedures to resolve routine issues.
JOB COMPLEXITY: Works on problems of limited scope. Follows standard practices and procedures in analyzing situations or data from which answers can be readily obtained. Builds stable working relationships internally.
SUPERVISION: Normally receives detailed instructions on all work.
EXPERIENCE :Typically requires no previous professional experience.
This position has the authority and responsibility for:
The Manufacturing Supervisor may be assigned to work directly with Upstream, Downstream or Buffer Preparation Unit Operations. This individual will supervise a team of employees directly or indirectly in these production process units.
Position Summary: The Equipment Maintenance Technician IV on our 2nd Shift is an opportunity at Fujifilm Dimatix, Inc. in Lebanon, N.H. The Equipment Maintenance Technician IV is responsible for the maintenance of manufacturing equipment for production lines. Also responsible for troubleshooting and repairing downed equipment and may assist engineering staff in establishing and implementing periodic equipment maintenance. Technician may participate in safety forums, Emergency Response Teams and station improvement teams.
Position Summary: The Equipment Maintenance Technician 3rd Shift opportunity is at Fujifilm Dimatix, Inc. in Lebanon, N.H. The Equipment Maintenance Technician III is responsible for the maintenance of manufacturing equipment for production lines. Also responsible for troubleshooting and repairing downed equipment and may assist engineering staff in establishing and implementing periodic equipment maintenance. Technician may participate in safety forums, Emergency Response Teams and station improvement teams.
A proactive and driven team player is required to passionately support delivery and embedding of the Data Integrity projects at FUJIFILM Biotechnologies, Texas. The Quality Assurance (QA) Specialist II for Data Integrity will be responsible for the day to day running of the FUJIFILM Biotechnologies, Texas Data Integrity Program, performing data integrity assessments, gap confirmation and risk assessments, generate remediation plans and categorize gaps based on business priority and risks.
Reports to Senior Director, QA Compliance
Work Location College Station, TX
A proactive and driven team player is required to passionately support delivery and embedding of the Data Integrity projects at FUJIFILM Biotechnologies, Texas. The Quality Assurance (QA) Specialist III for Data Integrity will be responsible for the day to day running of the FUJIFILM Biotechnologies, Texas Data Integrity Program, performing data integrity assessments, gap confirmation and risk assessments, generate remediation plans and categorize gaps based on business priority and risks.
Reports to Senior Director, QA Compliance
Work Location College Station, TX
Position Description
We are hiring a Powder Milling & Cleaning Tech. The Powder Milling & Cleaning Tech will be responsible for the milling of powdered media and cleaning of powder media equipment.
This position is intended to perform administrative functions, sales functions, and activities to ensure the endoscopy sales region performs optimally. Develops, directs, and manages a strategic plan for the business model to ensure the region accomplishes the business plan and achieves corporate goals. Partner with the management team to ensure the best possible service and effective communications to employees and customers.
This role will cover the western US market. The ideal candidate will reside within one of these locations:
Denver
Phoenix
Las Vegas
Salt Lake City
Seattle
Portland
Bay Area
Los Angeles Area
San Diego
*MUST HAVE ENDOSCOPY EXPERIENCE
Act as the local Compliance Officer for both of FUJIFILM Biotechnologies sites in North Carolina region. In addition, they will be the main Compliance contact / support for any questions / requirements for FUJIFILM Biotechnologies.
Software Powered by iCIMS
www.icims.com