Quality Control Analyst jobs at FUJIFILM Diosynth Biotechnologies - 563 jobs
Associate Research Chemist
Fujifilm Diosynth Biotechnologies 4.0
Quality control analyst job at FUJIFILM Diosynth Biotechnologies
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 an Associate Research 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 Associate Research Chemist will be responsible for design, develop and commercialization of new semiconductor etchants, post etch selective cleaners and strippers for advanced technology.
Company Overview
FUJIFILM Electronic Materials, U.S.A. fuels innovation in the semiconductor industry-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.
We'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've got what it takes to build a more connected world? Then connect with us today and challenge the boundaries of what's possible-for the world and your future.
We have six U.S. manufacturing and Research & Development facilities, located in: Mesa, Arizona; Castroville, California; Hollister, California; Carrollton, Texas; and North Kingstown, Rhode Island-each offering unique local experiences, from vibrant cultural scenes to historic charm.
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 "giving our world more smiles." Visit: ***************************************************
Job Description
Key responsibilities for this role include:
* Responsible for applied research & development and commercialization of new post etch cleaners and selective etchants for advanced IC technologies.
* Responsibilities include designing, lab testing and managing new chemical products under rigorous business and customer timelines.
* Specific activities include:
* Investigate and develop new chemical formulations for cleaning integrated circuit wafers with awareness of the status of the intellectual property field.
* Perform wet bench formulation and testing of new chemicals to meet customer requirements.
* Manage existing product testing and qualification using customer wafers.
* Support thin film surface analysis using tools including Ellipsometer, 4-Point probe, XRR, XPS, TOF-SIMS, SEM.
* Assist with IP searches and initial patent drafts.
* Assist in pilot line builds of successful beaker formulations.
* Generating and communicating product data and technical reports internally and to customers
* Write and present internal presentation updating technical and business groups on project status.
REQUIREMENTS
* 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.
* Experience in developing and applying inorganic or organic solution chemistry to meeting customer requirements. Must be comfortable working safely with hazardous chemicals.
* Understanding Si wafer device processing in wet processing tool operation and process implementation.
* Experience with thin film surface analysis tools such as Ellipsometer, 4-Point probe, XRR, XPS, TOF_SIMS, SEM
* Must have a strong comprehension of surface cleaning methods and chemicals.
* Must be proficient in design of experiments, technical writing, literature search processes and methods and Intellectual property processes and methods.
* 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.
* 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.
ADDITIONAL REQUIREMENTS
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.
* Resilience -Ability to adapt to workplace challenges, maintain professionalism, and manage responsibilities effectively.
* Communication -Capacity to clearly and professionally exchange ideas, interact respectfully with colleagues and customers, and foster positive workplace relationships.
* Reasoning & Decision Making -Ability to analyze information, follow verbal and written instructions, and make logical, sound decisions.
* Comprehension -Capability to understand and complete tasks as assigned and solve problems effectively.
* Organizational Skills - Competence in managing multiple priorities, maintaining accuracy, and staying focused despite potential workplace distractions.
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.
EEO Information
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.
ADA Information
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 (********************************).
$75k-94k yearly est. Auto-Apply 60d+ ago
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Chemist
Pacer Group 4.5
Rahway, NJ jobs
Job Title: Chemist
Duration: 12 Months
Qualifications
Education Minimum Requirement: • BS/BA in chemistry or related scientific fields with 2-5 years of experience. Required Experience and Skills: • Familiar with common analytical instrumentation • Strong teamwork and interpersonal skills • Strong written and oral communication skills Preferred Experience and Skills: • Experience with analytical techniques such chromatography (HPLC) and dissolution and ability in trouble shooting these methodologies • Experience using Empower is a plus • Experiences with analytical work in the pharmaceutical industry, such as method development and validation. • Experience working in a GMP / GLP environment a plus.
Responsibilities
We are looking for an individual who will perform analytical testing to support drug product development. This will involve development and validation of analytical test methods, analytical testing for process development support, data processing, and summarizing/presenting results to the supervisor.
$43k-57k yearly est. 18h ago
Chemist
Pacer Group 4.5
Wilson, NC jobs
Job Title: Chemist
Duration: 06 Months
Pay Rate: $25/hr on W2
Shift: 7:00AM-5:30PM (Mon -Thurs) but there is some flexibility in start time
Performs a variety of chemical analyses and GMP review in accordance with cGMP, GLP, DEA and company policies and procedures.
Perform routine testing (dissolution, assay/degradant, content uniformity and ID) of drug products in a cGMP laboratory.
Complete all assigned testing in a timely and organized manner in accordance with cGMP, GLP, DEA and company policies and procedures.
Enter data into laboratory information system and accurately document all necessary and relevant information in a clear concise manner as per cGMPs.
Operate and maintain all analytical instrumentation and equipment as per established procedures; perform basic troubleshooting.
Communicate openly within the group to provide and gather information, to optimize the use of resources and to optimize efficiency.
Aid other group members as required.
Ensure that equipment and working areas are maintained with good safety and housekeeping practices.
Re-stock chemicals and consumables used in analysis.
Performs other related assignments and duties as required and assigned.
Skills:
Understanding of analytical technology (HPLC, GC, Dissolution, Automation, or Spectroscopy - UV/Vis, NIR, IR, or AA/AE).
Relevant experience may include academic and/or industry experience and is measured based on the quality and quantity of the experience as it relates to the requirements of the position.
Perform job functions in various positions that may require sitting, stooping, balancing, kneeling, crouching, twisting, and/or reaching. While sitting for an extended period of time on a routine basis, incumbent may use the following equipment: Personal computer, telephone/ other voice communication devices, copier, fax, scanners, or other specialized equipment used in an office setting.
Lift and maneuver equipment and materials weighing up to 20 pounds.
Take samples which may require stretching, bending, or twisting to remove product from the equipment and/or drums.
Use small hand and power tools to perform incidental maintenance.
Perform cleaning and assembly/disassembly on laboratory equipment which may require pulling, pushing, or twisting to remove equipment shields, parts and panels. Equipment and parts could weigh up to 20 pounds. Also requires operation of industrial hose (water) and physical exertion (repetitive wiping, rubbing and scrubbing) to clean equipment and laboratory surfaces.
Ability to work a 10 hour per day/4-day work week Monday through Thursday; 40 hours per week with overtime as required.
Education:
The incumbent must have a BA or BS degree in Chemistry or closely related science. Minimum of 1-year relevant experience preferred.
$25 hourly 2d ago
Quality Control Inspector
Delta Electronics Americas 3.9
Plano, TX jobs
Who We Are:
Delta, founded in 1971, is a global provider of power and thermal management solutions. Its mission statement, "To provide innovative, clean and energy-efficient solutions for a better tomorrow," focuses on addressing key environmental issues such as global climate change. As an energy-saving solutions provider with core competencies in power electronics and automation, Delta's business categories include Power Electronics, Mobility, Automation, and Infrastructure. Delta, founded in 1971, is a global provider of power and thermal management solutions. Its mission statement, "To provide innovative, clean and energy-efficient solutions for a better tomorrow," focuses on addressing key environmental issues such as global climate change. As an energy-saving solutions provider with core competencies in power electronics and automation, Delta's business categories include Power Electronics, Mobility, Automation, and Infrastructure. Delta, founded in 1971, is a global provider of power and thermal management solutions. Its mission statement, "To provide innovative, clean and energy-efficient solutions for a better tomorrow," focuses on addressing key environmental issues such as global climate change. As an energy-saving solutions provider with core competencies in power electronics and automation, Delta's business categories include Power Electronics, Mobility, Automation, and Infrastructure.
About the role:
The Quality Control Inspector is responsible for inspecting sheet metal parts, welded assemblies, and finished products to ensure compliance with engineering drawings, welding standards, and customer requirements. This role supports the manufacturing team by identifying nonconformities, ensuring corrective actions, and maintaining product quality throughout fabrication and welding processes.
Key responsibilities:
Perform dimensional inspections of sheet metal components using calipers, micrometers, height gauges, and other precision measurement tools.
Conduct visual and dimensional weld inspections per AWS D1.1, ISO, or equivalent welding standards.
Verify weld quality, including size, length, penetration, porosity, cracks, undercut, and overall workmanship.
Review and interpret engineering drawings, specifications, and weld symbols to ensure product conformity.
Perform in-process inspections during sheet metal fabrication (cutting, bending, stamping, drilling, assembly, etc.).
Inspect surface finishes, powder coating/painting, and other secondary processes
Document inspection results, prepare quality reports, and maintain records.
Support root cause analysis and corrective/preventive actions (CAPA)
Collaborate with production and engineering teams to resolve quality issues.
Ensure inspection tools and gauges are calibrated and properly maintained.
Follow all company safety, ISO 9001, and quality system procedures.
Minium Qualifications:
High school diploma or technical certification required, associate degree in a technical field preferred.
2+ years of experience in quality inspection within a sheet metal fabrication or welding environment.
Experience with precision measurement tools (calipers, micrometers, height gauges, CMM experience a plus).
Strong attention to detail and ability to work independently.
Good communication and documentation skills.
Preferred Qualifications:
Strong knowledge of welding processes (MIG, TIG, spot welding) and common weld defects.
Ability to read and interpret engineering drawings, GD&T, and weld symbols.
Familiarity with AWS D1.1 or similar welding standards; welding inspection certification (CWI, WI) preferred.
Understanding of ISO 9001 quality systems; IATF knowledge a plus.
Benefit at Delta Electronics Americas: Life at Delta
EEO Statement:
Delta Electronics Americas is an Equal Opportunity Employer and is committed to compliance with all applicable federal, state, and local laws. Delta Electronics America is committed to fostering a diverse, inclusive, and respectful workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, age, marital status, national origin, disability, veteran status, or any other protected characteristic.
The base salary range for this full-time position is 45k-55k per year. Actual pay will depend on factors such as location, skills, experience, market conditions, and business needs. This role may also be eligible for incentive pay, subject to the terms of the applicable plan. Eligible employees receive company-provided benefits in accordance with plan terms and eligibility requirements. Benefits include health coverage, wellness resources, retirement savings plan, paid time off, and other company‑sponsored programs; parental leave is provided in accordance with applicable law.
About the role:
The Quality Control Inspector is responsible for inspecting sheet metal parts, welded assemblies, and finished products to ensure compliance with engineering drawings, welding standards, and customer requirements. This role supports the manufacturing team by identifying nonconformities, ensuring corrective actions, and maintaining product quality throughout fabrication and welding processes.
Key responsibilities:
Perform dimensional inspections of sheet metal components using calipers, micrometers, height gauges, and other precision measurement tools.
Conduct visual and dimensional weld inspections per AWS D1.1, ISO, or equivalent welding standards.
Verify weld quality, including size, length, penetration, porosity, cracks, undercut, and overall workmanship.
Review and interpret engineering drawings, specifications, and weld symbols to ensure product conformity.
Perform in-process inspections during sheet metal fabrication (cutting, bending, stamping, drilling, assembly, etc.).
Inspect surface finishes, powder coating/painting, and other secondary processes
Document inspection results, prepare quality reports, and maintain records.
Support root cause analysis and corrective/preventive actions (CAPA)
Collaborate with production and engineering teams to resolve quality issues.
Ensure inspection tools and gauges are calibrated and properly maintained.
Follow all company safety, ISO 9001, and quality system procedures.
Minium Qualifications:
High school diploma or technical certification required, associate degree in a technical field preferred.
2+ years of experience in quality inspection within a sheet metal fabrication or welding environment.
Experience with precision measurement tools (calipers, micrometers, height gauges, CMM experience a plus).
Strong attention to detail and ability to work independently.
Good communication and documentation skills.
Preferred Qualifications:
Strong knowledge of welding processes (MIG, TIG, spot welding) and common weld defects.
Ability to read and interpret engineering drawings, GD&T, and weld symbols.
Familiarity with AWS D1.1 or similar welding standards; welding inspection certification (CWI, WI) preferred.
Understanding of ISO 9001 quality systems; IATF knowledge a plus.
Benefit at Delta Electronics Americas: Life at Delta
EEO Statement:
Delta Electronics Americas is an Equal Opportunity Employer and is committed to compliance with all applicable federal, state, and local laws. Delta Electronics America is committed to fostering a diverse, inclusive, and respectful workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, age, marital status, national origin, disability, veteran status, or any other protected characteristic.
The base salary range for this full-time position is 45k-55k per year. Actual pay will depend on factors such as location, skills, experience, market conditions, and business needs. This role may also be eligible for incentive pay, subject to the terms of the applicable plan. Eligible employees receive company-provided benefits in accordance with plan terms and eligibility requirements. Benefits include health coverage, wellness resources, retirement savings plan, paid time off, and other company‑sponsored programs; parental leave is provided in accordance with applicable law.
$33k-43k yearly est. 3d ago
2nd shift Quality Control Operator Level II
Stellar Industries Corp 3.5
Millbury, MA jobs
Job Description
About Us
Stellar Industries is a rapidly growing industry leader in manufacturing metalized ceramics. We are a major supplier of innovative, high-quality parts to the Aerospace, Photonics, Telecommunications, and Commercial industries. The company was acquired by TRUMPF Photonics in 2019 and has significant growth goals.
About the Role
The Quality Control Inspector Level II maintains quality standards by inspecting incoming materials from outside suppliers, in-process production, and finished products in accordance with the quality standards and operating procedures set forth by the Head of Quality Control/Quality Assurance.
What You Get to Do
Works independently with minimal supervision.
Maintain an organized and clean work area.
Uses Hand tools, including but not limited to tweezers, calipers, and micrometers.
Confirms specifications by conducting visual and measurement tests.
Works with a variety of blueprints and technical drawings; must be able to interpret changing requirements as products and builds vary.
Completes a General Inspection Report by documenting inspection findings regarding product dimensions, quantity of parts accepted/rejected, and basis of rejection.
Uses Vision Systems and documents results into the computer.
Follow all safety protocols.
Cross-train as requested in other areas of the company.
About You
Minimum of 3 years of quality control experience.
Must be able to work in a sitting position for up to 10 hours.
Must be able to wear a lab coat, spittle mask, and gloves while working.
The position requires working with measuring devices and microscopes.
Individuals must have previous experience working in a similar environment.
Must be able to work independently and demonstrate extremely high levels of precision and accuracy.
line, High-Temperature BTU Furnaces, as well as various facility-related items, including air handlers, air compressors, air filtration units, etc.
What We Offer
Competitive pay
A generous benefits package that includes medical, dental, 401K plan, and PTO
Employer-paid vision plan, Employer paid Basic Life and AD&D Insurance, and Employer Paid Disability Insurance
Tuition Reimbursement
4-Day workweek, Monday-Thursday 12 pm-10:30 pm
Monday-Thursday 12:00 pm - 10:30 pm
$34k-41k yearly est. 16d ago
Development Chemist - Liquid R&D: 1st Shift
Hentzen Coatings, Inc. 4.1
Batavia, IL jobs
Hentzen is a unique company in today's world. Since our founding in 1923, we've remained an independent, privately held organization committed to being a leader in the development and manufacturing of high-performance coatings. Our success is built on a foundation of innovation, dedication, and service-to both our customers and our employees. With over 100 years of experience, Hentzen has earned recognition as a technology leader and trusted partner in the aerospace, defense, and industrial markets. Our ability to custom-engineer advanced coatings tailored to meet the specific and challenging requirements of our customers sets us apart. This innovation comes to life in our state-of-the-art facilities, where our talented employees are empowered to solve complex problems through creativity and collaboration. If you're looking to join a company known for its technical excellence, employee commitment, and customer focus, Hentzen offers a rewarding and challenging opportunity to learn, grow, and make a meaningful impact.
DEVELOPMENT CHEMIST - LIQUID R&D
1st Shift M-F
Batavia, IL Plant
The Development Chemist - Liquid R&D is responsible for the formulation, research, and development of new products and colors as well as improvement of existing products.
The successful candidates will have an acceptable score on the color matching and math tests.
DESCRIPTION OF ESSENTIAL DUTIES:
Develop new products for customers per their requirements.
Develop products and solve technical issues with a relatively minor amount of direction.
Exercise wide discretion when solving challenges.
Provide technical assistance for existing accounts.
Build knowledge of analytical methods for solving problems.
Train production and quality control personnel.
Work with production personnel to solve problems.
Exhibit demonstrated decision-making abilities.
Plan activities for support personnel.
Reduce or rework distressed products on hand to reduce inventory.
Ability to travel up to 10% of time.
As part of the housekeeping procedures, the employee may be involved with the disposal of hazardous waste. The initial training of how to properly dispose of hazardous waste will be performed by the Environmental and Safety department or the department supervisor. Annual training of the same will be performed by the EHS department.
Perform other miscellaneous duties as assigned.
QUALIFICATION REQUIREMENTS:
Education level strongly preferred: Bachelor's degree in chemistry or related field.
Experience level preferred: One to three years in a manufacturing or industrial setting, preferably in coatings or chemical environment.
Ability to receive and provide instructions in a positive manner.
Ability to read, understand and apply complex mathematical calculations.
Exemplify core values, i.e., Integrity, Loyalty, Passion, Commitment, and Respect.
Must be a high energy, results driven individual with excellent communication, computer, and decision-making skills.
Ability to work independently, in a fast-paced team environment, with the proactive problem-solving skills and work ethic necessary for timely completion of projects.
Excellent computer skills (Microsoft Office - Word, Excel, Outlook), ERP system and other office machinery.
WORK ENVIRONMENT:
While performing the duties of this job, the employee is frequently required to talk and/or hear, stand, and/or walk, use hands to finger, handle or touch objects or controls, and move from place to place. The employee is regularly required to sit, balance, stoop, and occasionally reach above shoulders. The employee occasionally must use foot/feet to operate machinery, climb, or balance and reach above the shoulders. The employee may regularly lift and/or move up to 65 lbs.
Personal Protection Equipment is required during various processes in the production facility. Safety shoes, glasses, respirators, fire retardant uniform, and earplugs may be required when performing certain functions.
Please send your resume to:
Hentzen Coatings, Inc.
Attn: Human Resources
6937 W. Mill Road
Milwaukee, WI 53218
or
APPLY ONLINE AT:
Hentzen Career Center
Hentzen Coatings, Inc. is an Equal Opportunity Employer, including Veterans and Individuals with Disabilities.
***************
All candidates are subject to post-offer testing: including a job-related pre-employment physical, drug screen, and background check.
$51k-70k yearly est. Auto-Apply 45d ago
Development Chemist (at Gelest Inc.)
Mitsubishi Chemical Group 3.9
Morrisville, PA jobs
Gelest, Inc., part of the Mitsubishi Chemical Group, is hiring a Development Chemist to join our team in Morrisville, PA. This role offers the opportunity to contribute to our mission of delivering innovative specialty chemical solutions to customers worldwide.
The Development Chemist will play a key role in designing, developing, and optimizing chemical processes for specialty chemical products. This hands-on role involves synthetic organic chemistry, process development from lab to pilot scale, and data acquisition and analysis to ensure safe, reliable, and cost-effective manufacturing. The Development Chemist will collaborate closely with Product Development, Engineering, Production, and Quality teams to translate laboratory discoveries into scalable processes that meet business and regulatory requirements.
**PRINCIPAL ACCOUNTABILITIES:**
+ Design and perform laboratory experiments involving synthetic organic reactions, route evaluation, optimization, and troubleshooting.
+ Generate and analyze process data to identify improvement opportunities.
+ Scale laboratory processes to pilot and full production, ensuring robust transfer of technology and clear documentation.
+ Utilize analytical techniques (GC, NMR, FTIR, MS) to characterize materials, monitor reactions, and assess process performance.
+ Document experiments, observations, and recommended improvements in lab notebooks and technical reports.
+ Support process hazard assessments, safety reviews, and compliance with environmental, health, and safety regulations.
+ Maintain awareness of industry developments, new technologies, and specialty chemical manufacturing best practices.
+ Perform other duties as assigned.
**KNOWLEDGE/ EXPERIENCE/SKILLS:**
To perform the job successfully, an individual should demonstrate the following competencies:
+ Bachelor's degree in Chemistry, Chemical Engineering, or a related field. Master's degree preferred.
+ 1-3+ years of experience in specialty chemical synthesis, chemical process development, or scale-up preferred.
+ Hands-on experience with laboratory techniques and equipment preferred.
+ Background in synthetic organic chemistry, including multi-step synthesis and reaction mechanism understanding is preferred.
+ Experience with process development, including reaction kinetics, heat, and mass transfer, mixing, and scale-up considerations is preferred.
+ Hands-on experience with analytical instrumentation (GC, NMR, FTIR, MS) is preferred.
+ Excellent written and verbal communication, including technical reporting.
+ Commitment to maintaining a safe and compliant work environment.
+ Must be able to wear required PPE (safety shoes, glasses, gloves, hard hat; respirators as needed).
+ Must be able to climb ladders and stairs to collect samples and observe processes.
+ Must be able to lift up to 50 pounds and operate a forklift.
+ **Must be able to work 2nd shift:** Four (4) 10-hour shifts, Monday-Thursday, 12:30 PM - 11:00 PM
**Supplemental Company Information:**
Gelest, located in Morrisville, PA-conveniently accessible from Interstate 95, Route 1, and the PA/NJ Turnpikes-offers a rewarding career with competitive pay and a comprehensive benefits package, including:
+ Generous paid time off
+ Medical, Dental, Vision, and optional supplemental plans for employees and their families
+ 401(k) with a competitive company match
+ Company-paid Life Insurance, AD&D, Short-Term Disability, and Long-Term Disability
+ Eligibility for an annual performance bonus
+ Company-provided uniforms, work boots, and PPE
The salary range for this position is $27.00 (entry level) - $35.00 per hour. Factors such as scope and responsibilities of the position, candidate's work experience, education/training, job-related skills, internal peer equity, as well as market and business considerations may influence base pay offered. This salary will be subject to a geographic adjustment (according to a specific city and state), if an authorization is granted to work outside of the location listed in this posting.
$27-35 hourly 28d ago
Development Chemist III
Quaker Chemical Corporation 4.6
Conshohocken, PA jobs
At Quaker Houghton, we are experts in the development, production and application of chemical specialties, process fluids, lubricants and coatings for the manufacturing industry. We have been an integral part in the growth of the world's largest industrial companies and to this day our experience and expertise show in the actions and dedication of our Associates worldwide. Today, we have a global presence, with our corporate headquarters located in Conshohocken, PA. Quaker Houghton is a global publicly traded company with a unique collaborative culture that supports career growth for its associates and offers competitive compensation and benefit programs.
Summary:
Quaker Houghton is seeking a Development Chemist III to work in our Metalworking Fluid Development Laboratory in Conshohocken, PA. The laboratory supports multiple metalworking fluid product lines including soluble oils, semi-synthetics, and full synthetics. An individual in this role will be responsible for conducting product development, research projects, and product support for Quaker Houghton metalworking fluids. This will require working closely with commercial associates, other RD&E teams, customers, and external partners to design new products and execute tests both in the laboratory and in the field. We are seeking experienced candidates who are highly motivated, have strong collaboration skills, are creative problem solvers, and communicate effectively.
What will you do?
* Use knowledge of colloid chemistry, tribology, and testing techniques to formulate metalworking fluids that will meet customer needs and provide solutions to application problems.
* Work independently with minimal guidance from the laboratory manager.
* Act as a mentor to junior development chemists.
* Maintain a clear and orderly record all observations and data.
* Write detailed reports summarizing product development efforts, laboratory testing, and troubleshooting.
* Perform customer requested product analysis and testing to answer questions and address problems at commercial accounts.
* Provide legal and archival documentation for patent applications.
* Comply with safety regulations and lab procedures.
* Provide technical service and knowledge to customers and sales associates based upon the chemist's current level of expertise. Visit customers when required.
* Provide assistance to Manufacturing to improve the quality and efficiency of the manufacturing process. Assist Manufacturing and the Quality Assurance lab in solving quality and production problems.
* Comply with safety regulations and make recommendations towards the improvement of safety and environmental concerns.
* Follow all ISO quality and environmental standards as provided in the various procedural manuals. Ensure that all laboratory equipment is calibrated and functioning properly.
Education, Experience, Skills & Competencies:
* This position requires a Bachelor Degree in Chemistry or equivalent with at least 7 years of experience, a Master's Degree in Chemistry or equivalent with at least 5 years of experience, or a Doctor of Philosophy in Chemistry or equivalent with at least 3 years of experience.
* Knowledge of colloid chemistry, surfactants, and tribology is required.
* Experience with the formulation of metalworking fluids and field support of machining and grinding operations is highly desired.
* Understanding of applied statistics and experimental design is not required, but highly desired.
* Must have the ability to operate in a fast-paced environment, to work on different projects at the same time, and to think analytically.
* Must have good prioritization and communication skills (oral and writing).
* Ability to write detailed reports and presentations which may be used to inform high-ranking members of the Technical Community.
What's in it for you:
* Competitive pay programs with excellent career growth trajectory
* Opportunities to see your efforts contribute toward the success of the business
* Work for a global leader in the industrial process fluids industry
Quaker Houghton is an equal opportunity employer committed to creating a diverse workforce. Quaker Houghton provides equal employment opportunity for all qualified candidates. Quaker Houghton does not discriminate against any candidate for employment based on race, color, religion, sex, gender, gender identity or expression, affectional or sexual orientation, pregnancy, age, creed, ancestry, national origin, citizenship, marital or domestic partnership or civil union status, veteran's status, physical/mental disability, genetic information, or any other category protected by U.S federal, state, and/or local employment law. Furthermore, Quaker Houghton is committed to providing reasonable accommodations to qualified candidates with physical and/or mental disabilities. Applicants with a disability who need assistance applying for a position may email ************************.
$66k-85k yearly est. 60d+ ago
Lab Technician III, Microbiology
Leprino Foods Company 4.7
Denver, CO jobs
Within our Corporate Analytical Services team located in Denver - Leprino is seeking a Lab Technician III, Microbiology to move our organization to an even larger level of dairy ingredient and nutrition growth! We take pride in our vision to be "world's best", it is why we work harder, invest more, and continually innovate.
At Leprino, starting compensation for this role is typically $28.33. This position has an annual target bonus of 3.5%.
What You'll Do:
* Assist with the setup and cleanup of microbiological testing by labeling, pipetting, organizing, and preparing dairy and environmental samples.
* Keep lab equipment clean and ready for use-maintaining sterile tools is second nature to you!
* Operate the autoclave to sterilize glassware, waste, and media safely and efficiently.
* Dispose of test tubes and refill distilled water jugs to support day-to-day lab operations.
* Track inventory and supplies, ensuring everything is labeled, weighed, and organized by plant.
* Perform basic housekeeping duties to keep the lab in good working order.
* Coordinate with team members to maintain clear documentation and accurate records of sample prep and lab activities.
* Follow written procedures carefully and with accuracy to maintain integrity in the lab.
* Support a collaborative team focused on food safety and quality-your role helps feed families across the globe!
* Offer ideas for improving lab workflows, safety, or sample management-we want to hear them!
You Have At Least (Required Qualifications):
* A high school diploma or GED.
* Some exposure to microbiology or chemistry through school or work-enough to understand basic concepts and handle pipettes, balances, and related tools.
* Comfort following detailed instructions and keeping work areas orderly and accurate.
* A team-focused approach with clear communication and a willingness to learn.
* Work Schedule is Sunday-Wednesday, 10 hour shifts
We Hope You Also Have (Preferred Qualifications):
* An associate or bachelor's degree in microbiology, biology, or a related field.
* Hands-on experience working in a laboratory setting, especially in food or dairy.
* Familiarity with sterile technique, aseptic sample prep, or operating an autoclave.
* A track record of keeping things organized while juggling multiple tasks in a lab.
At Leprino, we believe in equal employment opportunity and make employment decisions based on each individual's unique talents, experience, skills, and knowledge; we do not discriminate on the basis of any personal characteristics. We know we are better together and are committed to creating an inclusive and supportive culture in which all employees can thrive.
Offering You In Return:
A chance to be part of a global team of individuals passionate about producing and delivering high-quality products that help feed and nourish families around the world. Leprino could not be where it is today without our incredible employees. That is why we share in our success together by rewarding you for your hard work. Hiring great people who are in it for the long run is our goal. Through competitive salaries and bonuses, life, medical/dental/vision coverage, voluntary benefits, employee assistance programs, wellness incentives, tuition assistance, vacation, ten paid holidays, sick time, paid parental leave, annual merit increases, as well as the LFC Profit-Sharing & 401(k) plan. Your impact will be noticed and rewarded, as you seek to further our company, our customers, and one another.
Our Story:
Leprino's history dates back to the 1950s, when Jim Leprino first started making small batches of mozzarella for local markets and eateries in the Little Italy neighborhood of Denver. We've grown a bit since then. Today, Leprino is the world's largest manufacturer of mozzarella and lactose, and a leading producer of whey protein. Still owned by the Leprino family, our sights are set to be the "World's Best Dairy Food and Ingredient Company." From a small corner grocery store we have grown to over 5,500 employees throughout the globe. Will you join us on our journey?
Leprino uses Psychemedics for a 90-day hair follicle drug test as a pre-employment screening tool and also participates in E-Verify. Some positions at the Denver corporate office may require Personal Protective Equipment (PPE) based on role and location.
$28.3 hourly 5d ago
Lab Technician III, Microbiology
Leprino Foods Company 4.7
Denver, CO jobs
Within our Corporate Analytical Services team located in Denver - Leprino is seeking a Lab Technician III, Microbiology to move our organization to an even larger level of dairy ingredient and nutrition growth! We take pride in our vision to be "world's best", it is why we work harder, invest more, and continually innovate.
At Leprino, starting compensation for this role typically is $28.33. This position has an annual target bonus of 3.5%.
What You'll Do:
* Assist with the setup and cleanup of microbiological testing by labeling, pipetting, organizing, and preparing dairy and environmental samples.
* Keep lab equipment clean and ready for use-maintaining sterile tools is second nature to you!
* Operate the autoclave to sterilize glassware, waste, and media safely and efficiently.
* Dispose of test tubes and refill distilled water jugs to support day-to-day lab operations.
* Track inventory and supplies, ensuring everything is labeled, weighed, and organized by plant.
* Perform basic housekeeping duties to keep the lab in good working order.
* Coordinate with team members to maintain clear documentation and accurate records of sample prep and lab activities.
* Follow written procedures carefully and with accuracy to maintain integrity in the lab.
* Support a collaborative team focused on food safety and quality-your role helps feed families across the globe!
* Offer ideas for improving lab workflows, safety, or sample management-we want to hear them!
You Have At Least (Required Qualifications):
* A high school diploma or GED.
* Some exposure to microbiology or chemistry through school or work-enough to understand basic concepts and handle pipettes, balances, and related tools.
* Comfort following detailed instructions and keeping work areas orderly and accurate.
* A team-focused approach with clear communication and a willingness to learn.
* Work Schedule is Wednesday-Saturday 7:30 AM-6 PM, 10 hour shifts
We Hope You Also Have (Preferred Qualifications):
* An associate or bachelor's degree in microbiology, biology, or a related field.
* Hands-on experience working in a laboratory setting, especially in food or dairy.
* Familiarity with sterile technique, aseptic sample prep, or operating an autoclave.
* A track record of keeping things organized while juggling multiple tasks in a lab.
At Leprino, we believe in equal employment opportunity and make employment decisions based on each individual's unique talents, experience, skills, and knowledge; we do not discriminate on the basis of any personal characteristics. We know we are better together and are committed to creating an inclusive and supportive culture in which all employees can thrive.
Offering You In Return:
A chance to be part of a global team of individuals passionate about producing and delivering high-quality products that help feed and nourish families around the world. Leprino could not be where it is today without our incredible employees. That is why we share in our success together by rewarding you for your hard work. Hiring great people who are in it for the long run is our goal. Through competitive salaries and bonuses, life, medical/dental/vision coverage, voluntary benefits, employee assistance programs, wellness incentives, tuition assistance, vacation, ten paid holidays, sick time, paid parental leave, annual merit increases, as well as the LFC Profit-Sharing & 401(k) plan. Your impact will be noticed and rewarded, as you seek to further our company, our customers, and one another.
Our Story:
Leprino's history dates back to the 1950s, when Jim Leprino first started making small batches of mozzarella for local markets and eateries in the Little Italy neighborhood of Denver. We've grown a bit since then. Today, Leprino is the world's largest manufacturer of mozzarella and lactose, and a leading producer of whey protein. Still owned by the Leprino family, our sights are set to be the "World's Best Dairy Food and Ingredient Company." From a small corner grocery store we have grown to over 5,500 employees throughout the globe. Will you join us on our journey?
Leprino uses Psychemedics for a 90-day hair follicle drug test as a pre-employment screening tool and also participates in E-Verify. Some positions at the Denver corporate office may require Personal Protective Equipment (PPE) based on role and location.
$28.3 hourly 25d ago
Chemist (Temporary) - R&D Formulation Support
Dermalogica 4.0
Carson, CA jobs
Do you want to build a stronger, more sustainable future and cultivate your career? Become a part of the Dermalogica Research and Development team. We are looking for a talented Chemist to be based at the Corporate Headquarters in Carson working on-site with the R&D department in a temporary capacity.
Role Overview
Seeking a temporary R&D Chemist to support bench scale formulation, batching, and stability placement for skincare products. This is a hands-on, execution focused role supporting active development programs in the lab.
Key Responsibilities
Prepare bench scale batches following established formulas and SOPs
Support stability setup including labeling, documentation, and sample placement
Accurately record batch data, observations, and deviations
Maintain lab organization, raw material handling, and equipment cleanliness
Partner with formulation and stability teams to support active projects
Required Skills & Experience
BS in Chemistry, Cosmetic Science, Chemical Engineering, or related field
1 3 years hands on formulation or lab experience (cosmetics or personal care preferred)
Strong bench skills including weighing, mixing, heating/cooling, and pH adjustment
Familiarity with stability programs and sample tracking
Detail-oriented with strong documentation and organizational skills
Able to work independently with clear direction
Proficient in Microsoft Office (Excel, Word, Outlook) for documentation and data entry
The position is based at the corporate headquarters in Carson, CA, and will be fully on-site, 5 days per week (no remote or hybrid). The pay rate for this role is $35 per hour.
Ready to make a meaningful impact and advance your career with a global brand revolutionizing the skincare industry? Apply now and complete your online application. All applications will be reviewed, and our HR team will contact you if your skills align with the position.
Dermalogica is an equal opportunity employer committed to fostering an inclusive culture where all employees are valued, supported, and empowered to succeed.
$35 hourly 28d ago
Chemist (Temporary) - R&D Formulation Support
Dermalogica LLC 4.0
Carson, CA jobs
Job Description
Do you want to build a stronger, more sustainable future and cultivate your career? Become a part of the Dermalogica Research and Development team. We are looking for a talented Chemist to be based at the Corporate Headquarters in Carson working on-site with the R&D department in a temporary capacity.
Role Overview
Seeking a temporary R&D Chemist to support bench scale formulation, batching, and stability placement for skincare products. This is a hands-on, execution focused role supporting active development programs in the lab.
Key Responsibilities
Prepare bench scale batches following established formulas and SOPs
Support stability setup including labeling, documentation, and sample placement
Accurately record batch data, observations, and deviations
Maintain lab organization, raw material handling, and equipment cleanliness
Partner with formulation and stability teams to support active projects
Required Skills & Experience
BS in Chemistry, Cosmetic Science, Chemical Engineering, or related field
1-3 years hands on formulation or lab experience (cosmetics or personal care preferred)
Strong bench skills including weighing, mixing, heating/cooling, and pH adjustment
Familiarity with stability programs and sample tracking
Detail-oriented with strong documentation and organizational skills
Able to work independently with clear direction
Proficient in Microsoft Office (Excel, Word, Outlook) for documentation and data entry
The position is based at the corporate headquarters in Carson, CA, and will be fully on-site, 5 days per week (no remote or hybrid). The pay rate for this role is $35 per hour.
Ready to make a meaningful impact and advance your career with a global brand revolutionizing the skincare industry? Apply now and complete your online application. All applications will be reviewed, and our HR team will contact you if your skills align with the position.
Dermalogica is an equal opportunity employer committed to fostering an inclusive culture where all employees are valued, supported, and empowered to succeed.
$35 hourly 22d ago
Development Chemist I
Quaker Houghton 4.6
Batavia, NY jobs
About Us
At Quaker Houghton, we are experts in the development, production and application of industrial process fluids, lubricants and coatings for the manufacturing industry. We have been an integral part in the growth of the world s largest industrial and manufacturing companies from aerospace and automotive to primary metal and energy. Today, we have a global presence, with our corporate headquarters located in Conshohocken, PA. Quaker Houghton is a global publicly traded company with a unique collaborative culture that supports career growth for its colleagues and offers competitive compensation and benefit programs.
Summary
As a Development Chemist, you will be responsible for executing development assignments, determinations and tests under the supervision of the manager/supervisor or in assistance to a senior level Chemist, in order to contribute to the:
Development or improvement of products in support of the strategic plan.
Investigation and utilization of raw materials in newly developed and existing products.
Resolving of customer related issues.
Project work is performed in cooperation with a variety of internal and external contacts.
The ideal candidate will have a strong foundation of Chemistry knowledge, perform well in a collaborative team environment, strong critical thinking skills, is comfortable presenting technical information to a group and has strong technical writing skills.
Essential Duties and Responsibilities
Develop and improve chemical products used in a variety of manufacturing and mechanical systems in order to enhance processes, safety and quality in order to meet customer needs and provide solutions to application problems.
Investigate applicability of new and replacement raw materials in order to enhance performance and minimize cost.
Evaluate and incorporate alternate raw materials in existing products.
Carry out clearly specified tests and determinations, in order to answer questions and address problems of customers. Develops and performs customer requested product analysis and testing.
Determine performance characteristics of competitive products using physical, instrumental and wet analysis techniques.
Clearly and orderly record all observations and data. Report results in a clear and concise manner to enhance technical exchange Provide legal and archival documentation for patent applications.
Develop or improve test methods to enhance R&R, efficiency and field performance predictability.
Additional Responsibilities
Provide technical service and knowledge to customers and sales associates based upon the chemist s current level of expertise. Visits customers when required.
Provide assistance to manufacturing in order to improve the quality and efficiency of the manufacturing process.
Assist manufacturing and the quality assurance lab in solving quality and production problems.
Comply with safety regulations and make recommendations towards the improvement of safety and environmental concerns.
Maintain equipment, glassware and workspace in order to keep them clean and well-functioning. Properly dispose of all laboratory waste. Participate in ensuring good management of laboratory equipment and storage spaces for chemicals and raw materials.
Follow all ISO quality and environmental standards as provided in the various procedural manuals. Ensure that all laboratory equipment is calibrated and functioning properly.
Education/Experience
This position requires at least a Bachelor Degree in Chemistry or equivalent. Must have the ability to work in a fast pace environment, to work at different projects at the same time, and to think analytically. In addition, must have good prioritization and communication skills (oral and writing). Must be involved, careful, precise, team player, flexible, result/customer oriented and takes initiative.
Language Ability
A good command of the English language is mandatory. Ability to read, analyze and interpret common scientific and technical journals, financial reports, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community.
Computer Skills
To perform this job successfully, an individual should have knowledge of Word Processing software; Spreadsheet software; Internet software and Database software.
Work Environment
While performing the duties of this job the employee may be exposed to fumes or airborne particles and toxic or caustic chemicals. The employee is occasionally exposed to work near moving mechanical parts. The associate must be able to safely work in a variety of potentially hazardous situations. The noise level in the work environment is usually moderate.
Physical Demands
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 carefully, and precisely manipulate samples, apparatus, and sensitive instruments. The employee is frequently required to stand and reach with hands and arms. The employee is occasionally required to walk sit and talk or hear. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision and ability to adjust focus.
In accordance with applicable pay transparency requirements, the expected pay rate for this position is $54,000 - $59,000. Actual pay will be adjusted based on experience, geographic location, and other job-related factors as permitted by law.
This position also qualifies for full benefits. Quaker Houghton offers a robust suite of benefits for our employees including a 401(k) plan (with matching), paid time off, health and life insurance, including dental and vision coverage, flexible spending accounts to help offset the cost of dependent care and/or health care expenses, employee assistance programs, and short-term and long-term disability.
Quaker Houghton is an equal opportunity employer committed to creating a diverse workforce.
Quaker Houghton provides equal employment opportunity for all qualified candidates. Quaker Houghton does not discriminate against any candidate for employment based on race, color, religion, sex, gender, gender identity or expression, affectional or sexual orientation, pregnancy, age, creed, ancestry, national origin, citizenship, marital or domestic partnership or civil union status, veteran s status, physical/mental disability, genetic information, or any other category protected by U.S federal, state, and/or local employment law. Furthermore, Quaker Houghton is committed to providing reasonable
accommodations to qualified candidates with physical and/or mental disabilities.
Applicants with a disability who need assistance applying for a position may email
************************
.
$54k-59k yearly 33d ago
Development Chemist I
Quaker Houghton 4.6
Batavia, NY jobs
Job Description
About Us
At Quaker Houghton, we are experts in the development, production and application of industrial process fluids, lubricants and coatings for the manufacturing industry. We have been an integral part in the growth of the world's largest industrial and manufacturing companies from aerospace and automotive to primary metal and energy. Today, we have a global presence, with our corporate headquarters located in Conshohocken, PA. Quaker Houghton is a global publicly traded company with a unique collaborative culture that supports career growth for its colleagues and offers competitive compensation and benefit programs.
Summary
As a Development Chemist, you will be responsible for executing development assignments, determinations and tests under the supervision of the manager/supervisor or in assistance to a senior level Chemist, in order to contribute to the:
Development or improvement of products in support of the strategic plan.
Investigation and utilization of raw materials in newly developed and existing products.
Resolving of customer related issues.
Project work is performed in cooperation with a variety of internal and external contacts.
The ideal candidate will have a strong foundation of Chemistry knowledge, perform well in a collaborative team environment, strong critical thinking skills, is comfortable presenting technical information to a group and has strong technical writing skills.
Essential Duties and Responsibilities
Develop and improve chemical products used in a variety of manufacturing and mechanical systems in order to enhance processes, safety and quality in order to meet customer needs and provide solutions to application problems.
Investigate applicability of new and replacement raw materials in order to enhance performance and minimize cost.
Evaluate and incorporate alternate raw materials in existing products.
Carry out clearly specified tests and determinations, in order to answer questions and address problems of customers. Develops and performs customer requested product analysis and testing.
Determine performance characteristics of competitive products using physical, instrumental and wet analysis techniques.
Clearly and orderly record all observations and data. Report results in a clear and concise manner to enhance technical exchange Provide legal and archival documentation for patent applications.
Develop or improve test methods to enhance R&R, efficiency and field performance predictability.
Additional Responsibilities
Provide technical service and knowledge to customers and sales associates based upon the chemist's current level of expertise. Visits customers when required.
Provide assistance to manufacturing in order to improve the quality and efficiency of the manufacturing process.
Assist manufacturing and the quality assurance lab in solving quality and production problems.
Comply with safety regulations and make recommendations towards the improvement of safety and environmental concerns.
Maintain equipment, glassware and workspace in order to keep them clean and well-functioning. Properly dispose of all laboratory waste. Participate in ensuring good management of laboratory equipment and storage spaces for chemicals and raw materials.
Follow all ISO quality and environmental standards as provided in the various procedural manuals. Ensure that all laboratory equipment is calibrated and functioning properly.
Education/Experience
This position requires at least a Bachelor Degree in Chemistry or equivalent. Must have the ability to work in a fast pace environment, to work at different projects at the same time, and to think analytically. In addition, must have good prioritization and communication skills (oral and writing). Must be involved, careful, precise, team player, flexible, result/customer oriented and takes initiative.
Language Ability
A good command of the English language is mandatory. Ability to read, analyze and interpret common scientific and technical journals, financial reports, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community.
Computer Skills
To perform this job successfully, an individual should have knowledge of Word Processing software; Spreadsheet software; Internet software and Database software.
Work Environment
While performing the duties of this job the employee may be exposed to fumes or airborne particles and toxic or caustic chemicals. The employee is occasionally exposed to work near moving mechanical parts. The associate must be able to safely work in a variety of potentially hazardous situations. The noise level in the work environment is usually moderate.
Physical Demands
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 carefully, and precisely manipulate samples, apparatus, and sensitive instruments. The employee is frequently required to stand and reach with hands and arms. The employee is occasionally required to walk sit and talk or hear. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision and ability to adjust focus.
In accordance with applicable pay transparency requirements, the expected pay rate for this position is $54,000 - $59,000. Actual pay will be adjusted based on experience, geographic location, and other job-related factors as permitted by law.
This position also qualifies for full benefits. Quaker Houghton offers a robust suite of benefits for our employees including a 401(k) plan (with matching), paid time off, health and life insurance, including dental and vision coverage, flexible spending accounts to help offset the cost of dependent care and/or health care expenses, employee assistance programs, and short-term and long-term disability.
Quaker Houghton is an equal opportunity employer committed to creating a diverse workforce.
Quaker Houghton provides equal employment opportunity for all qualified candidates. Quaker Houghton does not discriminate against any candidate for employment based on race, color, religion, sex, gender, gender identity or expression, affectional or sexual orientation, pregnancy, age, creed, ancestry, national origin, citizenship, marital or domestic partnership or civil union status, veteran's status, physical/mental disability, genetic information, or any other category protected by U.S federal, state, and/or local employment law. Furthermore, Quaker Houghton is committed to providing reasonable
accommodations to qualified candidates with physical and/or mental disabilities.
Applicants with a disability who need assistance applying for a position may email
************************
.
$54k-59k yearly 2d ago
Development Chemist I
Quaker Chemical Corporation 4.6
Batavia, NY jobs
About Us At Quaker Houghton, we are experts in the development, production and application of industrial process fluids, lubricants and coatings for the manufacturing industry. We have been an integral part in the growth of the world's largest industrial and manufacturing companies from aerospace and automotive to primary metal and energy. Today, we have a global presence, with our corporate headquarters located in Conshohocken, PA. Quaker Houghton is a global publicly traded company with a unique collaborative culture that supports career growth for its colleagues and offers competitive compensation and benefit programs.
Summary
As a Development Chemist, you will be responsible for executing development assignments, determinations and tests under the supervision of the manager/supervisor or in assistance to a senior level Chemist, in order to contribute to the:
* Development or improvement of products in support of the strategic plan.
* Investigation and utilization of raw materials in newly developed and existing products.
* Resolving of customer related issues.
Project work is performed in cooperation with a variety of internal and external contacts.
The ideal candidate will have a strong foundation of Chemistry knowledge, perform well in a collaborative team environment, strong critical thinking skills, is comfortable presenting technical information to a group and has strong technical writing skills.
Essential Duties and Responsibilities
* Develop and improve chemical products used in a variety of manufacturing and mechanical systems in order to enhance processes, safety and quality in order to meet customer needs and provide solutions to application problems.
* Investigate applicability of new and replacement raw materials in order to enhance performance and minimize cost.
* Evaluate and incorporate alternate raw materials in existing products.
* Carry out clearly specified tests and determinations, in order to answer questions and address problems of customers. Develops and performs customer requested product analysis and testing.
* Determine performance characteristics of competitive products using physical, instrumental and wet analysis techniques.
* Clearly and orderly record all observations and data. Report results in a clear and concise manner to enhance technical exchange Provide legal and archival documentation for patent applications.
* Develop or improve test methods to enhance R&R, efficiency and field performance predictability.
Additional Responsibilities
* Provide technical service and knowledge to customers and sales associates based upon the chemist's current level of expertise. Visits customers when required.
* Provide assistance to manufacturing in order to improve the quality and efficiency of the manufacturing process.
* Assist manufacturing and the quality assurance lab in solving quality and production problems.
* Comply with safety regulations and make recommendations towards the improvement of safety and environmental concerns.
* Maintain equipment, glassware and workspace in order to keep them clean and well-functioning. Properly dispose of all laboratory waste. Participate in ensuring good management of laboratory equipment and storage spaces for chemicals and raw materials.
* Follow all ISO quality and environmental standards as provided in the various procedural manuals. Ensure that all laboratory equipment is calibrated and functioning properly.
Education/Experience
This position requires at least a Bachelor Degree in Chemistry or equivalent. Must have the ability to work in a fast pace environment, to work at different projects at the same time, and to think analytically. In addition, must have good prioritization and communication skills (oral and writing). Must be involved, careful, precise, team player, flexible, result/customer oriented and takes initiative.
Language Ability
A good command of the English language is mandatory. Ability to read, analyze and interpret common scientific and technical journals, financial reports, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community.
Computer Skills
To perform this job successfully, an individual should have knowledge of Word Processing software; Spreadsheet software; Internet software and Database software.
Work Environment
While performing the duties of this job the employee may be exposed to fumes or airborne particles and toxic or caustic chemicals. The employee is occasionally exposed to work near moving mechanical parts. The associate must be able to safely work in a variety of potentially hazardous situations. The noise level in the work environment is usually moderate.
Physical Demands
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 carefully, and precisely manipulate samples, apparatus, and sensitive instruments. The employee is frequently required to stand and reach with hands and arms. The employee is occasionally required to walk sit and talk or hear. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision and ability to adjust focus.
In accordance with applicable pay transparency requirements, the expected pay rate for this position is $54,000 - $59,000. Actual pay will be adjusted based on experience, geographic location, and other job-related factors as permitted by law.
This position also qualifies for full benefits. Quaker Houghton offers a robust suite of benefits for our employees including a 401(k) plan (with matching), paid time off, health and life insurance, including dental and vision coverage, flexible spending accounts to help offset the cost of dependent care and/or health care expenses, employee assistance programs, and short-term and long-term disability.
Quaker Houghton is an equal opportunity employer committed to creating a diverse workforce. Quaker Houghton provides equal employment opportunity for all qualified candidates. Quaker Houghton does not discriminate against any candidate for employment based on race, color, religion, sex, gender, gender identity or expression, affectional or sexual orientation, pregnancy, age, creed, ancestry, national origin, citizenship, marital or domestic partnership or civil union status, veteran's status, physical/mental disability, genetic information, or any other category protected by U.S federal, state, and/or local employment law. Furthermore, Quaker Houghton is committed to providing reasonable accommodations to qualified candidates with physical and/or mental disabilities. Applicants with a disability who need assistance applying for a position may email ************************.
$54k-59k yearly 33d ago
Development Chemist I
Quaker Chemical Corporation 4.6
Batavia, NY jobs
About Us At Quaker Houghton, we are experts in the development, production and application of industrial process fluids, lubricants and coatings for the manufacturing industry. We have been an integral part in the growth of the worlds largest industrial and manufacturing companies from aerospace and automotive to primary metal and energy. Today, we have a global presence, with our corporate headquarters located in Conshohocken, PA. Quaker Houghton is a global publicly traded company with a unique collaborative culture that supports career growth for its colleagues and offers competitive compensation and benefit programs.
Summary
As a Development Chemist, you will be responsible for executing development assignments, determinations and tests under the supervision of the manager/supervisor or in assistance to a senior level Chemist, in order to contribute to the:
* Development or improvement of products in support of the strategic plan.
* Investigation and utilization of raw materials in newly developed and existing products.
* Resolving of customer related issues.
Project work is performed in cooperation with a variety of internal and external contacts.
The ideal candidate will have a strong foundation of Chemistry knowledge, perform well in a collaborative team environment, strong critical thinking skills, is comfortable presenting technical information to a group and has strong technical writing skills.
Essential Duties and Responsibilities
* Develop and improve chemical products used in a variety of manufacturing and mechanical systems in order to enhance processes, safety and quality in order to meet customer needs and provide solutions to application problems.
* Investigate applicability of new and replacement raw materials in order to enhance performance and minimize cost.
* Evaluate and incorporate alternate raw materials in existing products.
* Carry out clearly specified tests and determinations, in order to answer questions and address problems of customers. Develops and performs customer requested product analysis and testing.
* Determine performance characteristics of competitive products using physical, instrumental and wet analysis techniques.
* Clearly and orderly record all observations and data. Report results in a clear and concise manner to enhance technical exchange Provide legal and archival documentation for patent applications.
* Develop or improve test methods to enhance R&R, efficiency and field performance predictability.
Additional Responsibilities
* Provide technical service and knowledge to customers and sales associates based upon the chemists current level of expertise. Visits customers when required.
* Provide assistance to manufacturing in order to improve the quality and efficiency of the manufacturing process.
* Assist manufacturing and the quality assurance lab in solving quality and production problems.
* Comply with safety regulations and make recommendations towards the improvement of safety and environmental concerns.
* Maintain equipment, glassware and workspace in order to keep them clean and well-functioning. Properly dispose of all laboratory waste. Participate in ensuring good management of laboratory equipment and storage spaces for chemicals and raw materials.
* Follow all ISO quality and environmental standards as provided in the various procedural manuals. Ensure that all laboratory equipment is calibrated and functioning properly.
Education/Experience
This position requires at least a Bachelor Degree in Chemistry or equivalent. Must have the ability to work in a fast pace environment, to work at different projects at the same time, and to think analytically. In addition, must have good prioritization and communication skills (oral and writing). Must be involved, careful, precise, team player, flexible, result/customer oriented and takes initiative.
Language Ability
A good command of the English language is mandatory. Ability to read, analyze and interpret common scientific and technical journals, financial reports, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community.
Computer Skills
To perform this job successfully, an individual should have knowledge of Word Processing software; Spreadsheet software; Internet software and Database software.
Work Environment
While performing the duties of this job the employee may be exposed to fumes or airborne particles and toxic or caustic chemicals. The employee is occasionally exposed to work near moving mechanical parts. The associate must be able to safely work in a variety of potentially hazardous situations. The noise level in the work environment is usually moderate.
Physical Demands
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 carefully, and precisely manipulate samples, apparatus, and sensitive instruments. The employee is frequently required to stand and reach with hands and arms. The employee is occasionally required to walk sit and talk or hear. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision and ability to adjust focus.
In accordance with applicable pay transparency requirements, the expected pay rate for this position is $54,000 - $59,000. Actual pay will be adjusted based on experience, geographic location, and other job-related factors as permitted by law.
This position also qualifies for full benefits. Quaker Houghton offers a robust suite of benefits for our employees including a 401(k) plan (with matching), paid time off, health and life insurance, including dental and vision coverage, flexible spending accounts to help offset the cost of dependent care and/or health care expenses, employee assistance programs, and short-term and long-term disability.
Quaker Houghton is an equal opportunity employer committed to creating a diverse workforce. Quaker Houghton provides equal employment opportunity for all qualified candidates. Quaker Houghton does not discriminate against any candidate for employment based on race, color, religion, sex, gender, gender identity or expression, affectional or sexual orientation, pregnancy, age, creed, ancestry, national origin, citizenship, marital or domestic partnership or civil union status, veterans status, physical/mental disability, genetic information, or any other category protected by U.S federal, state, and/or local employment law. Furthermore, Quaker Houghton is committed to providing reasonable accommodations to qualified candidates with physical and/or mental disabilities. Applicants with a disability who need assistance applying for a position may email
$54k-59k yearly 34d ago
Development Chemist (at Gelest Inc.)
Gelest 4.1
Morrisville, NC jobs
Gelest, Inc., part of the Mitsubishi Chemical Group, is hiring a Development Chemist to join our team in Morrisville, PA. This role offers the opportunity to contribute to our mission of delivering innovative specialty chemical solutions to customers worldwide.
The Development Chemist will play a key role in designing, developing, and optimizing chemical processes for specialty chemical products. This hands-on role involves synthetic organic chemistry, process development from lab to pilot scale, and data acquisition and analysis to ensure safe, reliable, and cost-effective manufacturing. The Development Chemist will collaborate closely with Product Development, Engineering, Production, and Quality teams to translate laboratory discoveries into scalable processes that meet business and regulatory requirements.
PRINCIPAL ACCOUNTABILITIES:
Design and perform laboratory experiments involving synthetic organic reactions, route evaluation, optimization, and troubleshooting.
Generate and analyze process data to identify improvement opportunities.
Scale laboratory processes to pilot and full production, ensuring robust transfer of technology and clear documentation.
Utilize analytical techniques (GC, NMR, FTIR, MS) to characterize materials, monitor reactions, and assess process performance.
Document experiments, observations, and recommended improvements in lab notebooks and technical reports.
Support process hazard assessments, safety reviews, and compliance with environmental, health, and safety regulations.
Maintain awareness of industry developments, new technologies, and specialty chemical manufacturing best practices.
Perform other duties as assigned.
KNOWLEDGE/ EXPERIENCE/SKILLS:
To perform the job successfully, an individual should demonstrate the following competencies:
Bachelor's degree in Chemistry, Chemical Engineering, or a related field. Master's degree preferred.
1-3+ years of experience in specialty chemical synthesis, chemical process development, or scale-up preferred.
Hands-on experience with laboratory techniques and equipment preferred.
Background in synthetic organic chemistry, including multi-step synthesis and reaction mechanism understanding is preferred.
Experience with process development, including reaction kinetics, heat, and mass transfer, mixing, and scale-up considerations is preferred.
Hands-on experience with analytical instrumentation (GC, NMR, FTIR, MS) is preferred.
Excellent written and verbal communication, including technical reporting.
Commitment to maintaining a safe and compliant work environment.
Must be able to wear required PPE (safety shoes, glasses, gloves, hard hat; respirators as needed).
Must be able to climb ladders and stairs to collect samples and observe processes.
Must be able to lift up to 50 pounds and operate a forklift.
Must be able to work 2nd shift: Four (4) 10-hour shifts, Monday-Thursday, 12:30 PM - 11:00 PM
Supplemental Company Information:
Gelest, located in Morrisville, PA-conveniently accessible from Interstate 95, Route 1, and the PA/NJ Turnpikes-offers a rewarding career with competitive pay and a comprehensive benefits package, including:
Generous paid time off
Medical, Dental, Vision, and optional supplemental plans for employees and their families
401(k) with a competitive company match
Company-paid Life Insurance, AD&D, Short-Term Disability, and Long-Term Disability
Eligibility for an annual performance bonus
Company-provided uniforms, work boots, and PPE
The salary range for this position is $27.00 (entry level) - $35.00 per hour. Factors such as scope and responsibilities of the position, candidate's work experience, education/training, job-related skills, internal peer equity, as well as market and business considerations may influence base pay offered. This salary will be subject to a geographic adjustment (according to a specific city and state), if an authorization is granted to work outside of the location listed in this posting.
$27-35 hourly Auto-Apply 11d ago
Quality Control Inspector
The Gund Company 4.0
Amsterdam, NY jobs
Join The Gund Company, where you will find friends who will support and challenge you to crush goals that provide amazing growth opportunities. We are in the business of electrical insulation manufacturing, but we really pride ourselves in just being a group of fun, driven, problem solvers who LOVE what we do!
The Gund Company: Take Care of Each Other, Take Care of the Customer and Take Care of the Business
Job Summary
The Quality Inspector works under the supervision of the Quality Specialist or Regional Quality Manager and Plant Manager to provide quality assurance and quality control support for The Gund Company. The Quality Inspector executes activities associated with inspection and quarantine of nonconformance activities of The Gund Company products. The role supports execution of the quality management system (QMS) at an individual manufacturing site within a global multi-site QMS. Team members work closely with the Quality Specialist and Regional Quality Managers to comply with customer specific requirements and to maintain quality control requirements.
Essential Job Functions
Process execution a of quality assurance (QA), quality control (QC), and continuous improvement (CI) process at assigned site.
Execute in process, first article, PPAP, and other customer defined inspections.
Support process engineering in process capability studies and audits.
Drive improvement and customer focuses responsiveness to quality issues for assigned site.
Other duties as assigned.
Requirements:
Supervisory Responsibilities
This position does not have supervisory responsibilities.
Qualifications & Skills
Understand appropriate gauging practices to ensure specifications of attribute, variable, and transfer gauges.
Strong computer skills especially with Microsoft Word, Excel, and Power Point
Prior experience with data entry and report analysis in an Enterprise Resource Planning (ERP) system.
Willingness to develop project management skills.
Keeps rigorous records with an eye for detail.
Ability to communicate expectations and instructions to team members.
Ability to identify root cause, develop creative solutions to problems and continuously improve systems and processes.
Experienced and blueprint reading and application of appropriate measurement systems.
Ability to train operators on appropriate inspection methodology.
Education & Experience
American Society of Quality Certifications, but not required: Certified Quality Inspector.
Travel
Travel may be required up to 5% of the time.
Physical Demands
To perform this job successfully, the physical demands listed are representative of those that must be met by an employee. 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 sit, stand, walk, use hands to handle and feel, reach with hands and arms, talk, and hear. The position will be required to be in manufacturing facilities.
Disclaimer: The above statements are intended to describe the general nature and level of work being performed by those assigned to a particular position. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required and personnel may be required to perform duties outside their normal responsibilities from time to time, as needed.
Why Join Us?
Our employees have a vested interest in our Companys success. The Gund Company is
30% employee-owned
through our ESOP (Employee Stock Ownership Plan). Shares are awarded each year based on a calculation that takes into consideration our Companys financial profitability, employee tenure, and earnings. There is no out-of-pocket investment required!
In addition, our employees enjoy:
A safe and healthy work environment
Competitive wages
Comprehensive, cost-effective employee benefits: Health, Dental, Vision, Life, and Disability
401(k) retirement savings program with a 50% employer match up to 6% of contributions
Regular employee feedback through our IDP (Individual Development Plan)
According to the Gallup Q12 employee survey method, The Gund Company is ranked world-class regarding employee engagement. Please review our current career opportunities and consider applying today! We are always accepting applications for new talent to join our organization.
EEO Statement: It is the policy of The Gund Company to recruit, hire, train, and promote employees without discriminating based on race, gender, age, religion, national origin, veteran status, sexual preference, or disability.
Disclaimer: The above statements are intended to describe the general nature and level of work being performed by those assigned to a particular position. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required and personnel may be required to perform duties outside their normal responsibilities from time to time, as needed.
PIf88baea86ec7-31181-39387423
RequiredPreferredJob Industries
Other
$24k-42k yearly est. 10d ago
Powder Formulation Technician - 3rd Shift
Fujifilm Diosynth Biotechnologies 4.0
Quality control analyst job at FUJIFILM Diosynth Biotechnologies
We are hiring a Powder Formulation Technician. The Powder Formulation Technician will be responsible for formulation of powdered media. 3rd Shift: 9:00 pm- 5:30 am At 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's biggest health challenges.
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're ready to make an impact, your future belongs with us at FUJIFILM Biosciences.
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.
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 "giving our world more smiles." Visit: ***************************************************
Job Description
Responsibilities:
* Formulates Powder media formulas per manufacturing protocols utilizing various weighing equipment such as scales and balance.
* Uses Mettler-Toledo IND780 terminal system in conjunction with the SAP ERP system to ensure correct raw materials assigned in the batch record are weighed at the specified quantity.
* Suggest changes in departmental procedures and processes (SOPs) as needed.
* Performs and documents line clearance at the start of each formulation event.
* Maintains all required logs and associated documentation.
* Assures that all chemicals are stored and labeled properly.
* Performs process scale checks on all required equipment including scales and balances.
* Keeps work area, utensils, tanks, mills, and equipment clean and organized.
* Ensures that supplies needed such as weigh boats, gloves, lab coats, etc. are well stocked in their designated areas. Orders supplies or informs Lead/Supervisor if supplies need to be ordered.
* Follows all safety procedures and works in a safe manner including wearing all required personal protective equipment.
* Understands and follows procedures to ensure that chemicals are handled properly.
* Good understanding of metric system and its conversions.
* Follows and actively participates in sustaining the 6S program in the area.
* Other duties as requested by Lead or Supervisor.
Required Skills/Education:
* High School Diploma or equivalent.
* Background in medical devices, diagnostics, food/vitamin processing, or pharmaceuticals.
* 1-2 years of hands on experience
* General education about chemicals and proper handling (college level science preferred).
* Working knowledge of metric system.
* Good understanding of current Good Manufacturing Practices (cGMPs).
* Ability to speak, read, and write English.
* Good oral and written communication skills.
Salary and Benefits:
* For California, the base salary range for this position is $19.65 - $25.51 per hour. Compensation for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience, location, etc.).
* Medical, Dental, Vision
* Life Insurance
* 401k
* Paid Time Off
* #LI-onsite
EEO Information
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.
ADA Information
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 (*****************).
$19.7-25.5 hourly Auto-Apply 2d ago
Med Lab Technician - Microbiology - Per Diem 8 Hour Rotating Shift (Non-Exempt) (Union)
Usc 4.3
California jobs
The Tech-Med Lab assists the Clinical Laboratory Scientist by performing routine specimen processing and analysis under direct supervision. The Technician may perform routine automated analysis, instrument checks, calibration, maintenance and quality control; under the direct supervision of a Licensed Clinical Laboratory Scientist on duty. Duties of Technicians also involve clerical functions such as answering telephone inquires and communicating with outside clients as well as reference laboratories utilized by the hospital.
Essential Duties:
Report directly to the CLS on duty.
Performs daily checks and maintenance.
Performs a variety of manual, semi-automated and automated Biochemical, Hematological, Microbiological and/or Blood Bank analysis on varied patient specimens, maintaining a high degree of accuracy and productivity.
Recognizes normal, abnormal and critical results and taking appropriate action as required, including appropriate considerations for the age of the patient.
Demonstrates proficiency in clerical and computer functions, for communicating results and for carrying out additional clinical and clerical duties to meet the needs of the Department.
Assures results are available within defined TAT guidelines
Communicates and interacts effectively with co-workers, guests of the Institution and hospital clinical staff.
Participates in the Department's Quality Assurance Program and continuing education sessions.
Help monitor supply levels, communicating with the supervisor for supplies that are needed, assisting in monitoring inventory, as assigned
Adheres to Safety / Infection Control guidelines using personal protective equipment as required
Willingness to take on new tasks and additional responsibilities
Displays flexibility to cover the lab in emergencies and difficult staffing situations.
Obtains specimens from designated patients as necessary.
Maintains an English speaking environment in all work areas
Obtains blood sample specimens by venipuncture or capillary methods in response to requests for testing by clinicians, with appropriate consideration for the age of the patient.
Receives and screens specimens with regard to acceptability as defined by established guidelines.
Responsible for processing, distributing or packaging all specimens received (except Blood Bank and Anatomic Pathology samples).
Handles all inquiries for lab results, specimen status and general information regarding the Department and its functions.
Performs other related duties as assigned or requested by the CLS or supervisor.
Adheres to established Hospital and Departmental policies and procedures.
Performs other duties as assigned.
Required Qualifications:
Req High school or equivalent
Req 1 year Experience in phlebotomy in an Acute Care Facility setting.
Req Organization/time management skills.
Req Demonstrate excellent customer service behavior.
Req Demonstrates excellent verbal and written communication skills.
Preferred Qualifications:
Pref Clinical Laboratory Specialist in Chemistry (ASCP) ASCP certification.
Required Licenses/Certifications:
Req Fire Life Safety Training (LA City) If no card upon hire, one must be obtained within 30 days of hire and maintained by renewal before expiration date. (Required within LA City only)
The hourly rate range for this position is $26.39 - $44.88. When extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate's work experience, education/training, key skills, internal peer equity, federal, state, and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations.
USC is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other characteristic protected by law or USC policy. USC observes affirmative action obligations consistent with state and federal law. USC will consider for employment all qualified applicants with criminal records in a manner consistent with applicable laws and regulations, including the Los Angeles County Fair Chance Ordinance for employers and the Fair Chance Initiative for Hiring Ordinance, and with due consideration for patient and student safety. Please refer to the Background Screening Policy Appendix D for specific employment screen implications for the position for which you are applying.
We provide reasonable accommodations to applicants and employees with disabilities. Applicants with questions about access or requiring a reasonable accommodation for any part of the application or hiring process should contact USC Human Resources by phone at **************, or by email at *************. Inquiries will be treated as confidential to the extent permitted by law.
Notice of Non-discrimination
Employment Equity
Read USC's Clery Act Annual Security Report
USC is a smoke-free environment
Digital Accessibility
If you are a current USC employee, please apply to this USC job posting in Workday by copying and pasting this link into your browser:
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$26.4-44.9 hourly Auto-Apply 3d ago
Learn more about FUJIFILM Diosynth Biotechnologies jobs