Summary:

The QC Project Coordinator I will construct, maintain, and oversee the Quality Control Testing Schedule to include release testing, stability testing, and method qualification activities.

The Quality Control Coordinator, under general direction, will be responsible for implementing a Quality Control Master Schedule to guide QC activities supporting batch release and stability testing.  The position will also require frequent communication with the Analytical Development and Assay Method Transfer groups to coordinate and schedule method qualification activities.  The Coordinator will assist the QC Analyst’s and QC Management to navigate GMP documents through the EQMS system.  Close attention to detail is required to update the Master Schedule on a daily basis to ensure QC deadlines and milestones are met.  Other responsibilities may include but are not limited to: Compiling data for Batch Disposition.  Attending planning meetings as needed.  Communicating gaps and schedule changes to QC Area Managers. 

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 North Kingstown, RI facility for an R&D Chemist!

With state-of-the-art manufacturing facilities in the U.S., Europe, Taiwan, China, Korea and Japan, local sales offices throughout the world and on-site applications support, FUJIFILM Electronic Materials supplies the world's top tier semiconductor manufacturers with a broad array of products and services used throughout the semiconductor manufacturing process. 

The Role

The successful candidate will lead the development and optimization of new platforms for photoimageable dielectric materials. This role involves collaboration with central R&D and product technology teams to drive raw material selection and formulation improvements.

The ideal candidate will have a strong background in polymer synthesis and organic chemistry, with expertise in design, synthesis, and characterization of new materials. Additionally, the R&D Chemist will apply experimental design, problem-solving skills, and root cause analysis to innovate and enhance product performance, while providing support in troubleshooting material-related issues.

A proactive and driven team player is required to passionately support delivery and embedding of the Data Integrity projects at FDBT. The Quality Assurance (QA) Specialist II for Data Integrity will be responsible for the day to day running of the FDBT 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 

The QA Specialist III, QA Validation, will be responsible for the review and approval of commissioning/qualification/validation protocols, reports, computer automation validation protocols and final reports and discrepancies for Quality Assurance. The QA Compliance Specialist III, QA Validation, will handle all associated responsibilities in compliance with Fujifilm quality policies and site SOPs to ensure regulatory compliance.

Reports to                Manager, QA Validation

Work Location         College Station, TX 

We have opportunities for Manufacturing Associates at several levels within our Drug Substance production teams.   

These roles will execute manufacturing processing steps and associated activities when operational. You will also participate in operational readiness projects and commissioning/qualification projects. Our brand-new facility will be 24/7 operational. We will have a day shift and a night shift. We are hiring for night-specific roles; however, all roles may require flexibility with working hours and/or shift.

We operate on a 2-2-3, 12 hour shift schedule (days or nights).

*** Please note that this posting represents multiple openings *** 

Member of the HCUS Solution and Product Planning team managing various aspects of product development and commercialization for the Fujifilm Healthcare Americas Corporation IT portfolio. The Global Product Manager (GPM) is responsible for developing product plans, acting as a Product Owner (PO) and coordinating relevant departments (stakeholders) to execute the plans and meet the plan’s objectives. The GPM reports to the Manager, Product Planning and is able to fill in and provide direction to the team as necessary in the absence of the Manager and or LPO.

The QA Specialist III, QA Compliance, will be responsible for the review and approval of commissioning/qualification/Compliance protocols, reports, computer automation Compliance protocols and final reports and discrepancies for Quality Assurance. The QA Compliance Specialist III, QA Compliance, will handle all associated responsibilities in compliance with Fujifilm quality policies and site SOPs to ensure regulatory compliance.

Reports to                Manager, QA Compliance

Work Location         College Station, TX 

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 Mesa, AZ facility for a Wet Lab Technician!

The Role

The Wet Lab Technician will be responsible for mixing and testing CMP slurries, operating wet lab characterization tools; executing test plans, generating test data, and maintaining CMP equipment.

The Maintenance Technician II, under the supervision of the Facilities Maintenance Supervisor, or designated supervisor will be responsible for performing various aspects of utilities, facilities and process equipment maintenance, utilities operation and support for the Texas Biological Facility (TBF), the Flexible Biological Facility (FBF) and the National Center for Therapeutic Manufacturing (NCTM) on behalf of Fujifilm Diosynth Biotechnology Texas (FDBT).

Primary responsibilities include various aspects of maintenance, utilities operation and support for facilities, utility equipment and biotech processing equipment.

This position will be required to use technical manuals, on-line resources and OEM representatives to maintain the equipment operational with a minimum of downtime. Strict adherence to Standard Operating Procedures (SOPs), cGMPs and Quality Standards in a Pharmaceutical Manufacturing facility are mandatory.

The Senior Automation Engineer 1, MES provides support to the Drug Product Finished Goods Manufacturing (DPFG) facility. This includes implementation of changes to the Automation systems, updating design documents, executing testing, troubleshooting events, and being a part of Automation on-call support. This role leads projects and handle complex changes while coordinating with other internal and external groups.

As a Senior Mechanical Engineer (Transducers), you will play a key role in designing innovative ultrasound transducers in a fast-paced environment. This position demands a focus on high-performance products that flawlessly meet the needs of our users. You'll need a strong foundation in mechanical engineering principles, including Design for Excellence (DFX) methodologies, expertise in low to mid-volume manufacturing of intricate electro-acoustic devices, a deep knowledge of materials and their appropriate finishes, thermal management techniques, and the ability to design and implement specialized tooling and fixtures for precise manufacturing. You'll also be responsible for developing and implementing rigorous testing procedures to ensure product quality. You'll leverage your industry experience to provide technical project leadership and guidance. This includes performing physical and statistical analyses, reviewing design specifications to ensure that product requirements are clearly defined and met, analyzing acoustic performance and feedback data to inform design improvements for both mechanical and tooling components, and collaborating with the manufacturing team to translate design improvements into tangible benefits.

The Account Executive, ES (Territory - New Hamphire, Vermont, Maine) is responsible for the generation of sales revenue for the organization through personal interaction with prospective customers within a given territory. This position is expected to promote the use of core products within prospective customer accounts, maintain current customer accounts to ensure a solid reference base and educate the general market on the benefits of the product. This position must establish a solid network of reference with “partner” representatives who supply the same customers with non-competitive products and maintain a thorough understanding of competitive products and competitive positioning to ensure success and become a true “Endoscopic Consultant” for the customer. Has overall responsibility in achieving a 10% annual increase of market share.

We are hiring a Liquid Packaging Technician. The Liquid Packaging Technician will be responsible for product inspection, labeling, case packaging, accountability and quarantine of sterile filled product.

Shift: 2nd shift- 1pm-9:00pm

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 North Kingstown, RI facility for a Senior Raw Materials Engineer!

The Role

The Senior Raw Materials Engineer ensures that the chemical manufacturing process operates efficiently and safely by managing the sourcing, testing, and quality assurance of raw materials.

This position involves strategic supplier selection, rigorous quality control, and close collaboration with cross-functional teams to optimize material performance, reduce costs, and ensure regulatory compliance.

The QA Engineer, DSM Operations (Night) is responsible to help drive the Quality oversight for the direction of all Drug Substance Manufacturing processes during the night shift. This role collaborates within the DSM Quality team as well as with other cross-functional teams. Ensures that all DSM systems and processes are operated/maintained as intended, with a focus on consistent policy administration, QA oversight of activities occurring during your shift and resolution or mitigation of issues occurring during operation. 

The Associate Director of Technical Marketing is a strategic role with global span requiring significant technical and scientific expertise, excellent communication skills, experience in a biopharma CDMO services and ideally either experience in marketing strategy, scientific communications strategy, or a technical sales environment. 

The individual will support a wide range of global marketing activities and thought leadership scientific/technical communications aligned with the Company business and marketing strategy to promote and expand FUJIFILM Diosynth Biotechnologies’ (FDB) presence in the global marketplace. 

The Quality Assurance (QA) Analyst II, under general direction, will be responsible for review and/or approval of basic and technical documentation; Drafting and reviewing of internal Quality policies and procedures; Assisting in and performing product related activities; Assisting in and performing Quality audit functions; Identifying process and Quality System improvements; Acting as a QA liaison internally.

Reports to                Supervisor/Manager, QA

Work Location         College Station, TX