Qureos Mentor

FujiFilm

<div>Position Overview:
<div>
The Sr. Manager - Facilities Maintenance, under the leadership of the Director of Facilities, will be responsible for managing the day-to-day utilities operations, maintenance strategies, repairs and troubleshooting support, outages response and vendor management on behalf of FLBT. Facilities, utilities and process equipment includes but are not limited to bioreactors, incubators, filtration skids, chromatography skids, autoclaves, freezers, refrigerators, walk-in cold rooms, QC/PD lab equipment, MCRs, MBUs, water purification and distillation units, air compressors and dryers, process gases, air handling units, air cooled chillers, steam/condensing boilers, wastewater treatment systems, among others. This position will also provide support during new facilities and equipment installation, working with the corresponding Engineering, Calibration, Operations, Automation, Validation and Quality department personnel, and with the various contractors and consultants working on the projects. This position will work closely with Environment, Health and Safety (EHS) to develop and ensure a safe workplace is developed; with Procurement/Facilities Support for development of repair parts and spare parts strategies; and with Engineering for the technical background, installation, improvement, and reliability of the Facilities and equipment.</div>
Job Description:
<div><b>
Es</b><b>s</b><b>e</b><b>n</b><b>t</b><b>i</b><b>a</b><b>l</b><b> </b><b>F</b><b>u</b><b>n</b><b>c</b><b>ti</b><b>on</b><b>s:</b></div><ul><li>
Responsible for taking a leadership role in the day-to-day operations of the maintenance group, able to handle multiple priorities quickly and efficiently and delegating tasks to appropriate trades and skill levels.</li><li>
Responsible for evaluating, developing, scheduling and/or conducting training to facilities, utilities and/or maintenance personnel about new or existing equipment/systems and ensure such training is reflected in current SOPs and other procedures (PMs, Calibrations, etc.) as required.</li><li>
Support Reliability Centered Maintenance (RCM) activities including condition monitoring and predictive technologies as applicable.</li><li>
Responsible to respond and support outages and plant-wide emergencies.</li><li>
Responsible to support facilities, utilities, and equipment IQ/OQ/PQ or any other validation activity as required.</li><li>
Ensure accurate documentation of maintenance activities such as PM, CM and emergency work orders through adherence of cGDP.</li><li>
Maintain regular communication with production and support area counterparts to ensure planned maintenance activities are executed effectively and any issues are addressed promptly.</li><li>
Communicate effectively with Contractors, Validation, Quality Assurance, Quality Control, Operations, Engineers, OEM providers, as well as internal equipment owners and operators, for successful management of the facilities department in FLBT.</li><li>
Ensure compliance, as set forth in internal quality protocols and SOPs including cGMP and FDA regulatory guidelines, within the areas of responsibility.</li><li>
Able to work with other engineers and validation contractors in directing and providing oversight of specialized contractors to ensure facility and equipment are delivered and/or maintained as prescribed.</li><li>
Develop, implement, maintain, and monitor departmental KPIs to ensure a high level of efficiency.</li><li>
Responsible for all Facilities/Utilities areas SOPs, PMs, JHA&rsquo;s.</li><li>
Ensure departmental cGMP compliance by staying current with assigned SOPs, maintaining up-to-date training files, and meeting all mandatory training requirements, including ADP courses.</li><li>
Ensure a safe work environment is maintained through adherence and compliance with safety guidelines, policies, and site procedures.</li><li>
Demonstrate continuous personal pursuit to increasing job knowledge, proficiency in technical understanding, and problem-solving abilities.</li><li>
Maintain a positive, professional, and customer-oriented attitude.</li><li>
Hire, train, develop and evaluate maintenance operations staff. Take corrective action as necessary on a timely basis and in accordance with Company policy. Ensure compliance with current federal, state, and local regulations in consultation with the Director of Facilities and Human Resources as appropriate.</li><li>
All other duties as needed.</li></ul><div></div><div><b><br>
Re</b><b>q</b><b>ui</b><b>r</b><b>ed</b><b> </b><b>S</b><b>k</b><b>ill</b><b>s</b><b> </b><b>&amp;</b><b> </b><b>A</b><b>b</b><b>i</b><b>l</b><b>i</b><b>t</b><b>i</b><b>e</b><b>s</b><b>:</b></div><ul><li>
Strong leadership qualities and skills.</li><li>
Strong understanding of plant and clean utilities system operation and applicable cGMP requirements with the ability to instruct and guide others on those requirements.</li><li>
Strong understanding of cGMP requirements and design for clean rooms including HVAC pressure cascades, pressurization, room air changes and environmental controls.</li><li>
Strong technical troubleshooting / problem solving skills. Possess or could gain knowledge with respect to the operation and maintenance of various utilities / process systems and be able to transmit all this knowledge to direct reports and peers.</li><li>
Knowledge of a wide variety of typical maintenance tasks including corrective maintenance, troubleshooting systemic problems and the tools and equipment required to perform these maintenance tasks.</li><li>
knowledge using blueprints, equipment manuals, specifications, standard operating procedures, and be able to use proper judgement when taking corrective actions during equipment malfunction.</li><li>
Must be able to generate and manage Change Controls and perform Deviation investigations.</li><li>
Must be able to develop clear procedures for equipment, utilities and maintenance operations.</li><li>
Knowledge of NFPA 70E requirements for safe work practices and be able to guide direct reports and contractors in such requirements.</li><li>
Knowledge of FDA, OSHA, EH&amp;S, EPA, and state of Texas requirements and be able to guide direct reports and contractors in such requirements.</li><li>
Knowledge and understanding of OSHA regulations, and safe work practices.</li><li>
Strong written, verbal and interpersonal communications skills.</li><li>
Desire to work in a fast paced, state of the art, alternately research and customized manufacturing facility.</li><li>
Ability to work quickly and effectively without constant supervision. Ability to lead a combination of 10+ maintenance supervisors / skilled technicians in support of facility maintenance.</li><li>
Working knowledge of MS Office products (Word, Excel, Outlook, and PowerPoint).</li><li>
This role will require a high level of personal organizational skills, experience, and drive. The successful candidate must have a vision of a final state, fully organized Facilities Maintenance department in a highly regulated GMP environment.</li><li>
Knowledge of preventative maintenance development using a GMP Computerized Maintenance management System (CMMS) required.</li></ul><div></div><div><b><br>
W</b><b>o</b><b>r</b><b>ki</b><b>n</b><b>g</b><b> </b><b>Co</b><b>n</b><b>di</b><b>ti</b><b>on</b><b>s</b><b> </b><b>&amp;</b><b> </b><b>P</b><b>h</b><b>y</b><b>sic</b><b>a</b><b>l</b><b> R</b><b>e</b><b>q</b><b>ui</b><b>r</b><b>em</b><b>e</b><b>n</b><b>ts:</b></div><div>
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to:</div><ul><li>
Engage in prolonged periods of sitting, standing, walking, bending, stooping, and stretching.</li><li>
Utilize hand-eye coordination and manual dexterity to operate portable tools, test instruments, computer keyboard, telephone, calculator, and other office equipment.</li><li>
Regularly lift and move objects weighing up to 50 pounds.</li><li>
Climb ladders and stairs of varying heights.</li><li>
Work under conditions that may be wet or humid.</li><li>
Provide support during off shifts, weekends, and holidays as needed.</li><li>
Work in outdoor weather conditions and noisy environments.</li><li>
Offer 24/7 support for company activities.</li><li>
Maintain mandatory attendance.</li></ul><div></div><div><b><br>
Minimum </b><b>Q</b><b>u</b><b>a</b><b>li</b><b>f</b><b>ications</b><b>:</b></div><ul><li>
Bachelor&rsquo;s degree in a maintenance/facilities or related discipline with a minimum of eight (8) years of qualified experience in a maintenance/facilities or related role within a pharma/biotech manufacturing facility or equivalent, preferably regulated by FDA or any other regulatory agency, OR</li><li>
Associate&rsquo;s degree in a maintenance/facilities or related discipline with a minimum of ten (10) years of qualified experience in a maintenance/facilities or related role within a pharma/biotech manufacturing facility or equivalent, preferably regulated by FDA or any other regulatory agency, OR</li><li>
High school diploma or general education degree (GED) in a maintenance/facilities or related discipline with a minimum of twelve (12) years of qualified experience in a maintenance/facilities or related role within a pharma/biotech manufacturing facility or equivalent, preferably regulated by FDA or any other regulatory agency</li><li>
A minimum of five (5) or more years of previous leadership experience.</li></ul><div></div><div><b><br>
Preferred Qualifications:</b></div><ul><li>
Knowledge of Blue Mountain Regulatory Asset Manager CCMS/CMMS.</li><li>
Knowledge of Trackwise quality management software.</li><li>
Knowledge of bio-processing equipment, and single use technology.</li><li>
Experience with development of technician training / qualification program.</li><li>
A wide range of maintenance and trade experience is a plus, including mechanical/electrical systems, variable frequency drives, pumps, electric motors, and PLC operations.</li></ul><div></div><div><i><br>
To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.</i></div></div><div></div>

Sr Manager, Facilities Maintenance

<div>Position Overview:
<p>
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.</p><p><br>
</p>Company Overview:
<p>
The work we do at FUJIFILM Biotechnologies Texas has never been more important&mdash;and we are looking for passionate, mission-driven people like you who want to make a real difference in people&rsquo;s lives.</p><br>
<p><br>
From developing the next vaccine to advancing cell and gene therapies, we collaborate with industry leaders to tackle complex challenges and deliver meaningful solutions.</p><br>
<p><br>
If you&rsquo;re ready to help transform the future of medicine, join FUJIFILM Biotechnologies. We offer a flexible work environment and we&rsquo;re proud to cultivate a culture that will fuel your passion, energy, and drive&mdash;what we call Genki.</p><br>
<p><br>
Our state-of-the-art biomanufacturing facility is located in in College Station, Texas, which combines a small-town feel with vibrant culture, top-notch schools, and close proximity to big city life. Nestled between major hubs, it&rsquo;s a dynamic location that blends convenience with innovation.</p><br>
<p><br>
Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of &ldquo;giving our world more smiles.&rdquo; Visit: https://www.fujifilm.com/us/en/about/region/careers</p>
Job Description:
<p><b>
Primary Responsibilities:</b></p><ul><li>
Collect environmental monitoring (Total Air, Viable Air and Viable Surface) in a cleanroom/controlled environment.</li><li>
Collect Utility Monitoring Samples (RODI/WFI) routinely and for qualification of systems.</li><li>
Sample Compressed Gas/Process Gas system.</li><li>
Autoclave materials and components for use in the QC laboratory.</li><li>
Routine QC laboratory cleaning</li><li>
Management of inventory items for the laboratory</li><li>
Ensure the lab is maintained (organized, clean, &amp; properly supplied).</li><li>
Perform other duties as assigned.</li></ul><div><b>
Qualifications:
</b></div><ul><li>Associate&rsquo;s degree preferably in Biochemistry, Chemistry, Biology, or related field; OR,</li><li>
High School Diploma or GED and 1+ year of relevant experience.</li><li>
Ability to analyze raw data, assess assay and system suitability criteria.
</li><li>Ability to follow safety procedures outlined in the Chemical Hygiene Plan.</li><li>
Utilize SDS sheets to properly assess chemical hazards, spill response procedures, and PPE requirements if indicated.</li><li>
Good attention to detail and ability to utilize problem solving/trouble shooting skills.</li><li>
Good computer skills.</li><li>
Demonstrated written and oral communication skills.</li><li>
Strong organization and analytical skills.</li><li>
Role model for company core values of trust, delighting our customers, Gemba, and Genki.</li></ul><div><b>
Physical Requirements:</b></div><p>
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to:</p><ul><li>
Experience prolonged standing, some bending, stooping, and stretching.</li><li>
Use hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment is required.</li><li>
Ability to sit for long periods to work on a computer.</li><li>
Potential for exposure to hazardous chemicals, gases, fumes, odors, mists, and dusts, and other hazardous materials.</li><li>
Ability to lift/pull/push 50 lbs on occasion and 15 lbs regularly.</li><li>
Ability to wear personal protective equipment including safety glasses, lab coat, and gloves.
</li><li>Attendance is mandatory.</li></ul><div><b>
Join us! FDB is advancing tomorrow&rsquo;s medicine, impassioning employees to chase the impossible and continually expand their potential. We are a company of emboldened goal seekers &ndash; driven by an innate desire to better ourselves, our families, our workplace, our company, our community and the world at large.</b></div><p></p><div><i><br>
To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.</i></div><br>
<div></div>
EEO Information:
<div>
Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.</div>
ADA Information:
<div>
If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBTHR@fujifilm.com or (979) 431-3500).</div></div>

QC Analyst I, Microbiology

<div>Position Overview:
<p>
The Quality Assurance (QA) Analyst III, under minimal direction, will be responsible for review and/or approval of basic and technical documentation, drafting and reviewing of internal Quality policies and procedures, performing product related activities, performing Quality audit functions, performing product release activities, identifying process and Quality System improvements, and acting as a QA liaison internally and externally.</p>
Company Overview:
<p>
The work we do at FUJIFILM Biotechnologies Texas has never been more important&mdash;and we are looking for passionate, mission-driven people like you who want to make a real difference in people&rsquo;s lives.</p><br>
<p><br>
From developing the next vaccine to advancing cell and gene therapies, we collaborate with industry leaders to tackle complex challenges and deliver meaningful solutions.</p><br>
<p><br>
If you&rsquo;re ready to help transform the future of medicine, join FUJIFILM Biotechnologies. We offer a flexible work environment and we&rsquo;re proud to cultivate a culture that will fuel your passion, energy, and drive&mdash;what we call Genki.</p><br>
<p><br>
Our state-of-the-art biomanufacturing facility is located in in College Station, Texas, which combines a small-town feel with vibrant culture, top-notch schools, and close proximity to big city life. Nestled between major hubs, it&rsquo;s a dynamic location that blends convenience with innovation.</p><br>
<p><br>
Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of &ldquo;giving our world more smiles.&rdquo; Visit: https://www.fujifilm.com/us/en/about/region/careers</p>
Job Description:
<p><b>
Reports to </b>Director, Quality Assurance/Senior Manager, Quality Assurance</p><p><b>
Work Location </b>College Station, TX (On-site at NCTM building)</p><p></p><p><b><br>
Primary Responsibilities:</b></p><ul><li>
Review and/or approve basic and technical documentation with minimal supervisory oversight to include, but not limited to:<ul><li>
Standard Operating Procedures</li><li>
Batch Production Records (completed and approval)</li><li>
Commissioning, qualification and validation protocols and reports</li><li>
Deviation Reports</li><li>
Corrective Action/Preventive Action Plans</li><li>
Technical data review and approval</li><li>
QC data review and approval</li><li>
Drug Substance/Product Reports</li><li>
Trending QA data</li></ul></li><li>
Draft and review internal Quality policies, procedures, and reports.</li><li>
Perform inspection of final product containers and review and/or approval of executed process records and data.</li><li>
Perform Quality audit functions to include, but not limited to:
<ul><li>Audit of lab notebooks</li><li>
Audit of equipment logbooks</li><li>
Review of vendor, supplier, contract laboratory audit questionnaires</li><li>
Lead vendor, supplier, contract laboratory and client audits</li><li>
Identify process and Quality System improvement opportunities.</li></ul></li><li>
Provide daily guidance for the compliance of the QA department to national and international standards and regulations.</li><li>
Support Regulatory, client, and internal audits.</li><li>
Act as QA liaison to internal Departments and external Client Quality Groups and Vendor/Contract Laboratory Quality Groups.</li><li>
Promptly notify Senior Management of potential quality or regulatory issues that may affect product quality or regulatory compliance.</li><li>
Assist with technical oversight/training for the QA team.</li><li>
Assist with compliance related functions.</li><li>
All other duties as assigned.</li></ul><div><b>
Qualifications:
</b></div><ul><li>Master&rsquo;s Degree and 1+ years&rsquo; experience in Pharmaceutical or other regulated industry.
</li><li>Bachelor&rsquo;s degree and 3+ years&rsquo; experience in Pharmaceutical or other regulated industry.
</li><li>Associates Degree and 5+ years&rsquo; experience in Pharmaceutical or other regulated industry.
</li><li>High school or equivalent and 8+ years&rsquo; experience in Pharmaceutical or other regulated industry.</li><li>
Certified Quality Auditor preferred.</li><li>
Degree in Biology or Chemistry preferred.</li><li>
Excellent written and oral communication skills.</li><li>
Excellent organizational, analytical, data review and report writing skills.</li><li>
Ability to set personal performance goals and provide input to departmental objectives.</li><li>
Ability to multitask and easily prioritize your work.</li><li>
Ability to work independently with little supervision.</li><li>
Proficient in Microsoft Excel, Word and PowerPoint.</li><li>
All candidates must have a working knowledge of cGMP regulations for the production of drug, biologics or vaccine products.</li><li>
Role model for company core values of trust, delighting our customers, and Gemba.</li></ul><div><b>
Physical Requirements:</b></div><p>
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to:</p><ul><li>
Experience prolonged standing, some bending, stooping, and stretching.</li><li>
Lifting up to 25 pounds on occasion.
</li><li>Use hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment is required.</li><li>
Attendance is mandatory.</li></ul><div><i>
To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.</i></div>
EEO Information:
<div>
Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.</div>
ADA Information:
<div>
If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBTHR@fujifilm.com or (979) 431-3500).</div></div>

QA Analyst III

<div><h2 class="jobSectionHeader"><b>Position Overview
</b></h2><div><div><div><p><b>Position Description</b></p><div><br>
</div><div>We are hiring a Equipment Maintenance Technician. The Equipment Maintenance Technician will perform general production, packaging, quality and research and development (R&amp;D) equipment repairs and maintenance to ensure the site meets cGMP and OSHA compliance. This employee is the on-site contact person for contractors and provides works including, but not limited to second shift, third shift on weekdays, weekends and holidays as assigned. They also respond to emergency production and packaging equipment troubleshooting needs.</div><div></div><div><b><br>
2nd Shift:</b> 1:00pm - 9:30pm
</div></div></div></div><h2 class="jobSectionHeader"><b>Company Overview
</b></h2><div><div><div><p>At FUJIFILM Irvine Scientific (dba FUJIFILM Biosciences), we turn curiosity into breakthroughs that advance the field of life sciences. By offering a comprehensive portfolio of products and services in cell culture media, discovery research reagents, recombinant growth factors and proteins, fine chemicals, and critical assay materials, we partner with the brightest minds in biotech and pharma to tackle the world&rsquo;s biggest health challenges.</p><br>
<p><br>
Imagine being part of a team that enables life-changing discoveries like new vaccines, therapies, and advancements in regenerative medicine. Our culture fosters curiosity, collaboration, and innovation, and we pride ourselves on delivering unparalleled quality and service to our partners. If you&rsquo;re ready to make an impact, your future belongs with us at FUJIFILM Irvine Scientific (dba FUJIFILM Biosciences).</p><br>
<p><br>
Our headquarters in Santa Ana, California, is surrounded by world-class schools, lush parks, and scenic beaches like Laguna and Huntington, making it an ideal place to live, work, and explore. With additional campuses across the US, Europe, China, and Japan, we offer opportunities to make a difference worldwide.</p><br>
<p><br>
Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of &ldquo;giving our world more smiles.&rdquo; Visit: https://www.fujifilm.com/us/en/about/region/careers</p>
</div></div></div><h2 class="jobSectionHeader"><b>Job Description
</b></h2><div><div><div><p><b>Responsibilities:</b></p><ul><li>
Documenting production equipment maintenance and repairs records in Computerized Maintenance System (CMS).</li><li>
Installing/maintaining/repairing/tuning/troubleshooting production and packaging equipment per planned schedule and work request.
</li><li>Evaluating equipment to identify and correct reasons for malfunctions.</li><li>
Repair production and packaging equipment. Technician with equipment PLC experiences is a plus.</li><li>
Requisitioning new supplies and equipment, as needed.</li><li>
May construct or fabricate parts from drawings or written instructions.</li><li>
Coordinating vendors and contractors as required.</li><li>
Moving equipment to meet operational needs.</li><li>
Responding to production, packaging, quality and research &amp; development (R&amp;D) equipment emergency needs.</li><li>
Must be willing to work in Second and Third shifts per assignment.</li><li>
May need to drive company vehicle if necessary.</li><li>
Manage Spare Parts.</li></ul><p><b>
Required Skills/Education:
</b></p><ul><li>HS. Diploma or equivalent, with trade school and/or formal training on equipment mechanics.</li><li>
5+ years&rsquo; work experiences in general facility production and packaging equipment maintenance and repair.</li><li>
Experience with Computerized Maintenance System (CMS). Proficiency of Windows including Outlook, Excel and Word.</li><li>
Ability to read, interpret, and work from electrical, mechanical diagrams and equipment manuals.</li><li>
Ability to work independently with no supervision.</li><li>
Equipment PLC experiences is a plus.</li><li>
Experience of working in GMP environment. Previous experiences in Pharmaceutical, Medical Devices and Biotechnology industries are pluses.</li><li>
Valid CA Driver License and good driving record
</li><li>Understand mechanical and electrical
</li><li>Working knowledge of cGMP and ISO 9001/EN46001.</li><li>
Knowledge of Equipment PLC operation is a plus.</li><li>
Ability to speak, read, write, and communicate clearly in English.</li></ul><div><b>
Salary and Benefits:</b></div><ul><li>
For California, the base salary range for this position is $28.16 - $36.66 per hour. Compensation for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience, location, etc.).</li><li>
Medical, Dental, Vision</li><li>
Life Insurance</li><li>
401k</li><li>
Paid Time Off</li></ul><ul><li>#LI-onsite<b>
</b></li></ul></div></div></div><h2 class="jobSectionHeader"><b>EEO Information
</b></h2><div><div><div><div>Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.</div>
</div></div></div><h2 class="jobSectionHeader"><b>ADA Information
</b></h2><div><div><div><div>If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (fisihr@fujifilm.com).</div></div></div></div></div>

Equipment Maintenance Tech

<div>Position Overview:
<div><b>
FUJIFILM Electronic Materials, U.S.A., Inc.,</b> 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 an <b>Associate Research Chemist!</b></div><div></div><div><br>
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.</div><div></div><div><b><br>
The Role</b></div><div></div><div><br>
The Associate Research Chemist will be responsible for design, develop and commercialization of new semiconductor etchants, post etch selective cleaners and strippers for advanced technology.</div>
Company Overview:
<p>
FUJIFILM Electronic Materials, U.S.A. fuels innovation in the semiconductor industry&mdash;where chemistry meets technology. Our advanced materials and formulations enable manufacturers to build the microchips that power Artificial Intelligence, computers, electric vehicles, smartphones, and more.</p><br>
<p><br>
We&rsquo;re a global business-to-business supplier of chemical formulations and advanced materials used for manufacturing and packaging semiconductors. Our chemical formulations allow top manufacturers to produce microchips that both power and connect our digital world. Think you&rsquo;ve got what it takes to build a more connected world? Then connect with us today and challenge the boundaries of what&rsquo;s possible&mdash;for the world and your future.</p><br>
<p><br>
We have six U.S. manufacturing and Research &amp; Development facilities, located in: Mesa, Arizona; Castroville, California; Hollister, California; Carrollton, Texas; and North Kingstown, Rhode Island&mdash;each offering unique local experiences, from vibrant cultural scenes to historic charm.</p><br>
<p><br>
Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of &ldquo;giving our world more smiles.&rdquo; Visit: https://www.fujifilm.com/us/en/about/region/careers</p>
Job Description:
<div><b>
Key responsibilities for this role include:</b></div><ul><li>
Responsible for applied research &amp; development and commercialization of new post etch cleaners and selective etchants for advanced IC technologies.</li><li>
Responsibilities include designing, lab testing and managing new chemical products under rigorous business and customer timelines.</li><li>
Specific activities include:<ul><li>
Investigate and develop new chemical formulations for cleaning integrated circuit wafers with awareness of the status of the intellectual property field.</li><li>
Perform wet bench formulation and testing of new chemicals to meet customer requirements.
</li><li>Manage existing product testing and qualification using customer wafers.</li><li>
Support thin film surface analysis using tools including Ellipsometer, 4-Point probe, XRR, XPS, TOF-SIMS, SEM.</li><li>
Assist with IP searches and initial patent drafts.</li><li>
Assist in pilot line builds of successful beaker formulations.</li><li>
Generating and communicating product data and technical reports internally and to customers</li><li>
Write and present internal presentation updating technical and business groups on project status.</li></ul></li></ul><div></div><div><b><br>
REQUIREMENTS</b></div><ul><li>
PhD in Chemistry with 1 to 5 years of experience in formulation. Prior industrial research experience in product development in semiconductor technology is highly prefered.</li><li>
Experience in developing and applying inorganic or organic solution chemistry to meeting customer requirements. Must be comfortable working safely with hazardous chemicals.</li><li>
Understanding Si wafer device processing in wet processing tool operation and process implementation.</li><li>
Experience with thin film surface analysis tools such as Ellipsometer, 4-Point probe, XRR, XPS, TOF_SIMS, SEM</li><li>
Must have a strong comprehension of surface cleaning methods and chemicals.</li><li>
Must be proficient in design of experiments, technical writing, literature search processes and methods and Intellectual property processes and methods.</li><li>
Must be a team player and collaborator. Must be able to communicate and work effectively with peers and customers. Organizational skills and prior project management experience desired.</li><li>
This is a safety-sensitive position that requires candidates to successfully pass a post-offer drug screening prior to employment. One of the essential job functions is the ability to work in a constant state of alertness and in a safe manner.</li></ul><div><br>
</div><div><b>ADDITIONAL REQUIREMENTS</b></div><div></div><div><br>
We value a professional, adaptable, and collaborative work environment. The following competencies are essential for success in any role and reflect our commitment to effective teamwork, problem solving, and workplace communication.</div><div></div><ul><li><b><br>
Resilience -</b>Ability to adapt to workplace challenges, maintain professionalism, and manage responsibilities effectively.</li><li><b>
Communication -</b>Capacity to clearly and professionally exchange ideas, interact respectfully with colleagues and customers, and foster positive workplace relationships.</li><li><b>
Reasoning &amp; Decision Making -</b>Ability to analyze information, follow verbal and written instructions, and make logical, sound decisions.</li><li><b>
Comprehension -</b>Capability to understand and complete tasks as assigned and solve problems effectively.</li><li><b>
Organizational Skills -</b> Competence in managing multiple priorities, maintaining accuracy, and staying focused despite potential workplace distractions.</li></ul><div></div><div><b><br>
To all agencies: Please, no phone calls or emails to any employee of Fujifilm about this requisition. All resumes submitted by search firms/employment agencies to any employee at Fujifilm via-email, the internet or in any form and/or method will be deemed the sole property of Fujifilm, unless such search firms/employment agencies were engaged by Fujifilm for this requisition and a valid agreement with Fujifilm is in place. In the event a candidate who was submitted outside of the Fujifilm agency engagement process is hired, no fee or payment of any kind will be paid.</b></div>
EEO Information:
<div>
Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.</div>
ADA Information:
<div>
If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (feus.humanresources@fujifilm.com).</div></div>

Associate Research Chemist