The Microbiologist I will be responsible for assisting the QC microbiological aspects of cGMP compliance and testing at the FUJIFILM Biotechnologies Texas Quality Control Laboratory. 

Reports to                Supervisor, Microbiology

Work Location         College Station, TX 

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.

Summary:  Under general direction, the Logistics Specialist II is responsible for the accurate receiving, packing, shipping, and external distribution of cGMP (current Good Manufacturing Practices) and non-GMP materials in support of company operations.

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.

Summary:  The Quality Assurance Program Quality Manager (QA PQM) is responsible for the operational oversight and execution of program quality requirements from the point of Quality Agreement signature through program closure. This role acts as the primary Quality liaison for assigned client programs, ensuring that program deliverables align with contractual commitments, quality standards, and regulatory requirements. Working in close collaboration with cross-functional teams, the Program Quality Manager helps ensure successful program outcomes through detailed coordination, compliance monitoring, and proactive issue resolution.

The purpose of this job is to provide comprehensive instrument and electrical (I&E) maintenance support throughout the FUJIFILM New Castle Site, ensuring reliable operation of manufacturing plants, labs, and warehouses. Responsibilities include handling I&E maintenance through daily work orders, carrying out preventative maintenance activities, conducting routine inspections and calibrations and progressing emergency repairs under the direction of the Maintenance and Facilities Manager.

The technician must have demonstrated I&E experience in a manufacturing environment, including the installation, calibration, and maintenance of instrument and control systems.

Incumbent is required to work safely and adhere to the site EHS guidelines while performing tasks and through the management of third-party contractors and work permits.

The Sr. Engineer, Supplier Quality provides supplier oversight to ensure that suppliers of services or materials to Fujifilm Diosynth Biotechnologies are of the highest quality while conforming to pre-established requirements including cGMPs. This role primarily focuses on supplier quality, working with suppliers to maintain supplier approvals. This role plays a key role in establishing the Supplier Quality System including but not limited to SOP and Specification development, Quality Agreements, Risk Assessments, Supplier Auditing and Supplier Change Notifications.

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 at our Pueblo, CO facility for a Production Supervisor - Processing!

The Role

The Production Supervisor - Processing will supervise the Pueblo manufacturing production area, providing reinforcement of key safety and operating protocols, training employees, managing process quality and output, system troubleshooting, managing transactions (where needed), and coordinating support from Pueblo Process Engineering. This individual will serve as the liaison between the Manufacturing Manager, Sr. Production Planners and Production/Processing personnel.

The Production Supervisor - Processing will review procedures, recommend and make improvements in processing/production operations through procedure edits and TWIs. This individual will train personnel, perform all supervisory functions for subordinate personnel and plan Processing/Production material requirements. This individual will participate in the FMEA, 8d investigations, and Control Plan process. Have the ability to generate NCMRs, and revise procedures. Must be 40-hour hazwoper trained.

This position is responsible for providing technical support, testing, repairing and configuring U/S machines The technical support will be primarily via the telephone, to personnel on all the organization’s Ultrasound products. This is the first-level ultrasound national technical support engineer position in the company.

The Regional Sales Associate is responsible for providing regional support to assigned Regional Sales manager.  This support includes Assisting Territory Managers in closing opportunities, ensuring shipment is complete and customer inquiries. This individual will be a highly motivated, self-starter.  Understands the needs of the Regional team and become an advocate for growth in the region.  May provide training and knowledge transfer support, as well as coverage when Territories are open and/or Territory Managers are on vacation. 

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

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.

The Regional Senior HR Business Partner plays a pivotal role in ensuring employee engagement and retention through the collaboration and strategic relationships built among employees and management of the North Carolina Region.  This role is a strategic business partner who “leans in” to ensure the needs of the business are met, balancing FUJIFILM Biotechnologies culture with the consistent implementation of policies and practices. The Regional Senior HR Business Partner is a leader who shows empathy with appropriate firmness while driving HR programs that focus on our people. This is a highly visible role working with all levels of the organization.

The Quality Assurance (QA) Analyst I, under direct supervision, will be responsible for assisting with the review and/or approval of basic and technical documentation; Drafting and reviewing of internal Quality policies and procedures; Assisting with product related activities; Assisting with Quality audit functions; Identifying process and Quality System improvements.

Reports to                Supervisor/Manager, QA

Work Location         College Station, TX