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The Sr. Associate Scientist, Process Development, is responsible for supporting the development and optimization of laboratory processes. This role ensures the integration of quality systems like LIMS and document management, manages laboratory inventory, and enhances processes through advanced knowledge of cell-based therapies and aseptic processing. The purpose of this role is to drive efficiency and accuracy in laboratory operations while maintaining compliance with regulatory standards.
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.
This position reports directly to the Senior Director of Marketing and has overall responsibility for instax™ product management and product marketing. Accountable for executing annual strategies and overseeing instax™ product staff (2), supporting both internal teams and external stakeholders (sales/retail partners).
The Director of Product Management for instax™ is responsible for leading the product team in the execution of all product related programs and owns the financial topline performance of the category.
We have an exciting opportunity at our North Kingstown, RI facility for a Warehouse Technician! The Warehouse Technician is responsible for shipping goods to customers and/or external warehouses and for providing materials and supplies to the manufacturing, laboratory, engineering and R&D groups for various activities. This is a 1st shift opportunity which will include shift differential pay in addition to our amazing benefits package!
The Senior Director, Media and External Relations role is part of the global Corporate Affairs team, supporting all of our sites around the globe. The role is essential in managing the company’s external communications and reputation, with a strong emphasis on building relationships with top-tier U.S. media outlets. You will be responsible for crafting and executing media strategies, monitoring media coverage, and creating content for our external channels. A key aspect of this role is collaborating with teams geographies Europe, US and Japan and functions such as finance, commercial, and investor relations, ensuring aligned messaging that resonates with key external audiences.
The Intern on the CQV team integrates into ongoing work, supporting building out the needed processes for execution of testing, reviewing documentation, and partnering with our leads to identify and drive opportunities for improvement.
Start Date: This internship is set to begin in May 2025 for an 11-week duration ending in August 2025.
Relocation: Please note this Internship Opportunity is designed to be 100% Onsite, 40 hours/week and a relocation/housing stipend is not provided.
The Director, Quality Systems and Support oversees and leads the QA Systems and Support function within FDBN. This includes, but is not limited to, managing team, ensuring the accuracy and timeliness of departmental deliverables, and upholding company core values. This role is also responsible for hosting and executing Quality site audits and regulatory inspections. Additionally, it supports QA Digital Technologies teams, Pharmaceutical Quality Systems, Application and Records Management, and Operational GMP Learning. This role ensures adherence to corporate policies and procedures for key quality subsystems (e.g., Business Process Owners for Change Management and Data Integrity) while maintaining quality systems in compliance with CGMP standards and regulatory requirements. All operations are conducted in accordance with executed training curricula and under appropriate quality systems such as ICH Q7, 21 CFR Part 820 and Part 11, EU GMP Volume 4, and enforcement of applicable FUJIFILM Diosynth Biotechnologies policies. This role fosters a strong Quality Culture across teams and contributes to cohesive implementation of quality systems at the Holly Springs site, aligning with organizational goals and regulatory expectations.
The Scientific Applications Specialist provides technical field support for existing and new products of VisualSonics and its ultra high frequency ultrasound and photoacoustic technology. The Applications Specialist role is to be a subject matter expert in preclinical ultrasound and photoacoustic imaging. They will demonstrate the value of VisualSonics products through successful sales demonstrations, customer education and training.
**This is a US based travel position; however, some international travel may be required**
Successful candidates will be currently located in the US near any major airport.
Summary: Under limited supervision of the Sr. Manager, Materials Management, the Warehouse Operations Manager, or the Manager, Warehouse Logistics, the Supervisor Materials Management is responsible for the assurance of accurate receipt, verification, record keeping, distribution, and or shipment of materials and goods. The supervisor position will be one of three focused areas: Receiving, Inventory Control/Picking, or Shipping. However, the Supervisor, Materials Management is expected to cross train and/or provide support to the other functional areas if needed.
The Environmental, Health & Safety (EHS) Specialist supports and implements the company’s Safety, Environmental, and Health Programs to ensure compliance with local, state, and federal regulations, as well as corporate policies. This role fosters a culture of safety and environmental stewardship while driving proactive measures, continuous improvement, and supporting EHS initiatives in laboratory and biosafety settings.
We have an exciting opportunity at our Mesa, Arizona facility for a QC Chemist! The QC Chemist serves as a Quality Control Specialist responsible for analyzing semiconductor materials in support of product qualification and to support all Quality Control laboratory processes.
We have an exciting opportunity at our Mesa, Arizona facility for a Manufacturing Technician in our CMP slurries group! The Manufacturing Technician - CMP supports receiving and cleaning containers, monitoring distillations, and packaging containers.
The Manufacturing Manager is a critical leadership position responsible for leading teams to execute clinical and commercial GMP cell therapy manufacturing activities such as media preparation, master cell banks, viral vectors, cell separation, autologous and allogeneic cell therapy. The Manufacturing Manager is accountable in ensuring manufacturing execution is performed in compliance with all required procedures and expectations are always meet, ensuring successful and complaint delivery of cell therapy technologies. This is a full time on site position.
The Engineer / Scientist 3 of Process Analytics provides support and leads technology transfer and technical oversight activities during manufacturing operations. This relates to process analytics data management systems, trending processes, and advanced analytic tools. This role leads junior team members through activities such as technology transfer, process impact assessments, and provides guidance as needed.
The QC Analytical Development (AD) Chemistry Scientist 2 is responsible for coordinating the transfer of analytical methods for Technology Transfer (TT) of drug substance (DS) and drug product (DP) into the Quality Control laboratories of FUJIFILM Biotechnologies Diosynth Holly Springs (FDBN). The QC AD Chemistry Scientist 2 ensures GMP compliant laboratory operations in accordance with regulatory guidelines. This role coordinates analytical method transfers from clients, including the following analytical methods: chromatography (GC, HPLC, UPLC, SEC), spectroscopy (MS, GC/MS, LC-MS/MS, UV, UV-Vis, FTIR), electrophoresis (GE, non-reducing and reducing CE-SDS, imaged capillary isoelectric focusing (icIEF)), wet chemistry, glycan analysis, sub-visible particle analysis, peptide mapping, and physical appearance, etc.
The QC AD Chemistry Sr. Analyst I works with limited direction to support the execution of analytical method transfers and validations for drug substance (DS) and drug product (DP) manufacturing into the Quality Control laboratories of FUJIFILM Biotechnologies Diosynth Holly Springs (FDBN). The analytical chemistry methods used in biological product manufacturing include chromatography, spectroscopy, electrophoresis, wet chemistry, glycan analysis, sub-visible particle analysis, peptide mapping, and physical appearance, etc. The QC AD Chemistry Sr. Analyst I adheres to GMP compliant laboratory operations in accordance with regulatory guidelines. This role executes analytical method transfers from clients and authors and reviews procedures, SOPs, and technical reports. The ability to effectively communicate and function in a fast-paced, highly technical environment is essential to success.
The Analytical Development (AD) Tech Transfer (TT) Scientist 2 manages and coordinates the transfer of drug substance and drug product QC analytical methods from customers into the large-scale manufacturing facility, from first campaign through commercialization (clinical through process performance qualification/commercial). This role interfaces with customers and cross-functional teams to scope analytical testing plans and achieve project milestones. This role authors/reviews transfer plans, method transfer documents, transfer summary reports and specification justification reports, as needed. This role effectively communicates and operates between different teams, ensuring compliance with regulations, and optimizing processes for efficient transfer of knowledge and technology.
The Technician 1, Maintenance is responsible for assisting 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 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.
QVS Engineering is a growing team whose mission is to improve the quality of FFSS products through their life-cycle, proactively handling component and module obsolescence while strategically reducing COGS (Cost of Goods Sold). The Senior Electrical Engineer (QVS) works with a cross-functional team to resolve complex ultrasound systems’ quality issues, defining and implementing innovative modifications to existing electrical designs to reduce cost while still maintaining high quality, and handling obsolescence of electrical/electronic components. Specific requirements include electronic troubleshooting experience using advanced lab equipment on circuit boards with large BGAs, expertise in power supplies/power converters, low power design, electronic component selection, and grounding schemes. Experiences in analyzing high speed signals, knowledge of standard buses including PCI express, USB and I2C, knowledge of memory technology, ASIC and FPGA are also required. Experiences with circuits that meet stringent EMI and RFI requirements are highly desired. Previous experience working with FDA-regulated products is highly desired.
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