Chemist jobs in Illinois

Scientist I – Analytical Chemistry (Pharmaceutical / GMP) Vernon Hills, IL (Onsite) Pay: Up to $35.79/hr Summaries and Responsibilities Summary: Hiring a Scientist I, Analytical Chemistry to support pharmaceutical analytical testing and technical documentation in an FDA-regulated, GMP environment. This role requires hands-on experience with wet chemistry and analytical instruments including HPLC, GC, UV-Vis, and titration.

Job Description Batchmaker/Mixer - IL Addison, IL • Production Description At ECOS®, we are a women-led company with a mission to create plant-powered laundry detergents and cleaners that are safer for people, pets and the planet. As a Climate Positive company, we restore more than 100% of its carbon, water, and energy use back to the earth, in our four manufacturing facilities right here in the USA. We have an immediate opening for Batchmaker to ensures the safe, quality, and consistent mixing of all production batches based upon orders received and stock levels. Key Job Functions: · Following batch making schedule and making all liquids necessary to fulfill orders · Taking all batch samples with corresponding batch sheet to Chemist for quality control · Reporting all problems and concerns with new and existing formulas to Chemist · Performing quality control in the lab as required to back-up Chemist and/or Lab Technician · Keeping all raw materials properly labeled and stored and in their proper location · Ensuring that all batch tanks, drums, pails, and lab samples are properly identified and labeled · Providing Purchasing with a weekly requisition for raw materials to be ordered · Reporting equipment breakdowns immediately to Plant Manager · Requesting all items needed to successfully perform job to Plant Manager · Ensuring housekeeping including a clean, organized batch area, in compliance with all safety regulations · Relocating chemicals received according to Deacom map · Handling other special projects and requests, as needed Requirements In order to be successful, you will need: · High school diploma/GED · Forklift Certified · Familiarity with chemical blending, along with ability to follow product formula instructions and understand Safety Data Sheets. · Ability to safely lift bottles, boxes, tools, equipment, and other necessary items · Ability to multi-task · Ability to manage time effectively · Detail oriented with the ability to read, comprehend, and follow instructions · Ability to manage time effectively and multitask Why join the ECOS Team: • Comprehensive group insurance including medical, dental, vision, short and long term disability, and supplemental insurance plans including accident and critical illness, • 401k with company match, • Paid vacation, • IL paid leave, • Eleven paid holidays per year including your birthday, • Paid parental bonding leave, • Sustainability incentives for purchasing eco-friendly car, • Wellness programs and incentives, • Equal Opportunity Employer/minority/female/disability/veteranCompany DescriptionJoin the ECOS Team! At ECOS®, we are a women-led company with a mission to create plant-powered laundry detergents and cleaners that are safer for people, pets and the planet. As a Climate Positive company, we restore more than 100% of its carbon, water, and energy use back to the earth, in our four manufacturing facilities right here in the USA.Join the ECOS Team! \r\n\r\nAt ECOS®, we are a women-led company with a mission to create plant-powered laundry detergents and cleaners that are safer for people, pets and the planet. As a Climate Positive company, we restore more than 100% of its carbon, water, and energy use back to the earth, in our four manufacturing facilities right here in the USA.

Job DescriptionDescription: Batchmaker/Compounder Full-time Addiosn, IL Description At ECOS®, we are a women-led company with a mission to create plant-powered laundry detergents and cleaners that are safer for people, pets and the planet. As a Climate Positive company, we restore more than 100% of its carbon, water, and energy use back to the earth, in our four manufacturing facilities right here in the USA. We have an immediate opening for Batchmaker to ensures the safe, quality, and consistent mixing of all production batches based upon orders received and stock levels. Key Job Functions: · Following batch making schedule and making all liquids necessary to fulfill orders · Taking all batch samples with corresponding batch sheet to Chemist for quality control · Reporting all problems and concerns with new and existing formulas to Chemist · Performing quality control in the lab as required to back-up Chemist and/or Lab Technician · Keeping all raw materials properly labeled and stored and in their proper location · Ensuring that all batch tanks, drums, pails, and lab samples are properly identified and labeled · Providing Purchasing with a weekly requisition for raw materials to be ordered · Reporting equipment breakdowns immediately to Plant Manager · Requesting all items needed to successfully perform job to Plant Manager · Ensuring housekeeping including a clean, organized batch area, in compliance with all safety regulations · Relocating chemicals received according to Deacom map · Handling other special projects and requests, as needed Requirements: In order to be successful, you will need: · High school diploma/GED · Forklift Certified · Familiarity with chemical blending, along with ability to follow product formula instructions and understand Safety Data Sheets. · Ability to safely lift bottles, boxes, tools, equipment, and other necessary items · Ability to multi-task · Ability to manage time effectively · Detail oriented with the ability to read, comprehend, and follow instructions · Ability to manage time effectively and multitask Starting Pay $23/hr Why join the ECOS Team: • Comprehensive group insurance including medical, dental, vision, short and long term disability, and supplemental insurance plans including accident and critical illness, • 401k with company match, • Paid vacation, • IL paid leave, • Ten paid holidays per year including your birthday, • Paid parental bonding leave, • Sustainability incentives for purchasing eco-friendly car, • Wellness programs and incentives, • Equal Opportunity Employer/minority/female/disability/veteran

Job DescriptionPosition: Research Chemistry Manager FLSA Classification: Exempt Schedule: Monday-Friday (40-45 hours minimum per week) Work Location: On-site in Champaign, IL Department: Operations What you should bring to the table: Obiter Research is seeking a highly motivated and organized Research Chemistry Manager to join our chemistry team! In this role, you will administer and manage the overall chemistry functions associated with Obiter Research, including: • Supplies and supports the activities associated with research and custom synthesis projects as well as FTEs accepted by the company., • Communicates with customers regarding the creation and issuance of quotes (RFQs) and Statements of Work (SOWs)., • Works with Executive Leadership to design and develop processes to enable a successful completion of accepted projects., • Upon acceptance of a project, a key accountability of this role will be to order needed chemicals and supplies necessary to complete the project., • Responsible for the organization and management of administrative functions as it relates to the communication and workflow from research chemistry throughout all other departments of the company including but not limited to Process development and Quality Control., • Serve as a special assistant to the COO/Supervising Chemist and/or CEO/Executive Chemist in Chemistry related matters., • Assures that all research chemists are trained and adhere to all company policies procedures and protocols including all areas of C.O.P.S.What we bring to the table:, • Competitive Pay & Total Rewards, • Medical, Dental, Vision, and Life Insurance - Starting after 30 days of employment, • Employee sponsored benefits including Short Term Disability and Life Insurance, • 401(k) Retirement Plan with Match to invest in your future wealth and retirement, • Paid Time Off and Holiday Pay to help you reset and come back refreshed, • The opportunity to work for a growing organization where you are valued have a direct impactRequirements:, • Must have a minimum of a Masters Degree (M.A.), with 8 to 12 years related experience, or a Doctorate (PhD) with 7 to 10 years related experience., • Must have experience working in a fast-paced environment with proven track record of balancing multiple projects and delivering needed results., • Experience in lab-scale process development of organic synthesis including reactions, purifications, and analysis techniques., • Strong interpersonal and communication skills to effectively influence inside and outside the organization at all levels, and among diverse teams., • Critical, creative thinker and idea generator with ability to convert ideas to proof-of-concept, inspire others to do the same., • Skilled in project management, especially in outlining initial scoping and proof-of-concept stages., • Business expertise; customer and market orientation. Able to translate commercial needs into technical programs and business opportunities, and drive to execution., • Ability to evaluate risk and recommend path forward., • Able to handle ambiguity, adapt to changing environments, overcome challenges, and set priorities., • Future thinking with a “whole systems” view.Work Environment:, • Obiter Research is a chemical manufacturing company, and your workstation is located in a manufacturing environment. You must be comfortable with sitting at a desk/working on a computer or standing and handling necessary manufacturing equipment for extended periods of time throughout the day.Obiter Research is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship. Obiter Research makes hiring decisions based solely on qualifications, merit, and business needs at the time. Job Type: Full-time Pay: $73,400.00 - $81,200.00 per year Benefits: • 401(k), • 401(k) matching, • Dental insurance, • Disability insurance, • Employee assistance program, • Health insurance, • Life insurance, • Paid time off, • Parental leave, • Professional development assistance, • Vision insurance, • Work from homePhysical setting:, • ManufacturingSchedule:, • 8 hour shift, • Day shift, • Monday to FridayAbility to commute/relocate:, • Champaign, IL 61822: Reliably commute or planning to relocate before starting work (Required)

Job Description A-Line Staffing is now hiring a Scientist I, Analytical Chemistry Development in Vernon Hills, IL 60061. The Scientist I would be working for a Fortune 500 pharmaceutical company and has career growth potential. This would be full-time / 40+ hours per week. Scientist I Compensation • The pay for this position is $35.79 per hour, • Benefits are available to full-time employees after 90 days of employment, • A 401(k) with a company match is available to full-time employees with 1 year of service on our eligibility dates Scientist I Highlights • This position is a contract assignment with potential to hire on permanently based upon attendance, performance, and business needs, • Monday-Friday schedule; standard business hours, • Onsite position located in Vernon Hills, IL, • Opportunity to work within a pharmaceutical analytical chemistry development environment Scientist I Responsibilities • Perform analytical chemistry testing and development activities in support of pharmaceutical products, • Utilize wet chemistry and instrumental analytical techniques including pH, titration, UV-Vis, GC, and HPLC, • Generate, review, and maintain scientific documentation in compliance with GMP requirements, • Author technical reports and other scientific documentation, • Troubleshoot analytical issues and implement effective solutions, • Interpret written, oral, diagrammatic, and schedule-based instructions, • Support laboratory investigations and method development activities, • Maintain compliance with FDA regulations, company policies, and laboratory procedures, • Manage multiple projects and priorities simultaneously while meeting deadlines Scientist I Requirements • Bachelor's or Master's Degree in Chemistry, Pharmaceutics, or a related scientific field, • 2-4 years of pharmaceutical analytical chemistry experience, • Experience with wet chemistry and instrumental analytical techniques (pH, titration, UV-Vis, GC, HPLC), • Experience working in an FDA-regulated environment, • Knowledge of GMP documentation requirements, • Excellent scientific writing and technical documentation skills, • Demonstrated knowledge of scientific methods and laboratory techniques, • Attendance is mandatory for the first 90 days Scientist I Preferred Qualifications • Master's Degree in Chemistry, Pharmaceutics, or related science discipline, • Experience supporting analytical method development and validation activities, • Strong troubleshooting and problem-solving abilities, • Ability to multitask and prioritize work in a fast-paced laboratory environment, • Strong communication and collaboration skills If the position is a good fit, apply to this posting today!

Job DescriptionJob Title: Analytical Chemist II Job Description The position of Analytical Chemist II is responsible for performing advanced analytical analysis of raw materials, in-process solutions, stability, finished goods, and cleaning samples, as well as providing general laboratory support. The role involves 50% laboratory testing using techniques such as FTIR and chromatography, and 50% responsibilities outside the laboratory, including Phase I investigations and data review. Responsibilities • Perform routine and non-routine analysis for raw materials, in-process solutions, stability, and finished goods, including identification testing, refractive index, density, viscosity, water activity, pH, appearance, taste, and smell testing., • Conduct advanced analytical testing such as limits tests, titration, water determination, assay, and impurities testing, along with ICP-MS testing., • Conduct pharmaceutical water testing, including nitrate testing, total organic carbon (TOC), and conductivity., • Analyze cleaning validation and surveillance samples., • Prepare solutions for routine and non-routine analysis, such as buffers and diluents., • Execute Phase I investigations., • Conduct simple data reviews generated from routine testing., • Coordinate samples prior to and following testing activities., • Order and stock laboratory supplies., • Perform laboratory maintenance activities, including equipment preventative maintenance, calibration, waste disposal, and cleaning laboratory areas., • Perform other activities as needed.Essential Skills, • Bachelor’s Degree in Chemistry or a related technical field., • Experience with HPLC and ICP-MS., • 4 years of experience working in a GxP laboratory environment., • Proficiency in Microsoft Office applications., • Strong written and oral communication skills in English., • Experience working in current Good Manufacturing Practice (cGMP) or other cGxP environments., • Experience with common laboratory equipment such as balances and graduated cylinders., • Experience with analytical methods such as chromatography and spectroscopy.Additional Skills & Qualifications, • Experience conducting laboratory investigations and reviewing routine testing data., • Experience using Laboratory Information Management System (LIMS).Work Environment The position is based in a QC Chemistry Lab with a team of 6-10 people on the Chemistry side. The lab is one of the few Analytical Chemistry labs in the nation. The QC team closely collaborates with the Micro team to ensure disposable product lines are properly tested before distribution to customers. The work involves active pharmaceutical ingredients for micro and chemistry labs at the Cary, IL site, including formulated products and disposables. The role operates on the 2nd shift from 12pm to 8pm. Job Type & Location This is a Contract to Hire position based out of Cary, IL. Pay and Benefits The pay range for this position is $34.00 - $38.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Cary,IL. Application Deadline This position is anticipated to close on Jun 30, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionChemist I – Quality Control (Weekend Day Shift) Build your chemistry career in a hands-on, high-impact lab environment About the Role Kickstart your career in chemistry with a role designed for growth, learning, and real-world impact. As a Chemist I, you’ll play a key role in ensuring the quality and safety of pharmaceutical products by performing analytical testing in a dynamic Quality Control (QC) laboratory. This position is ideal for recent graduates or early-career chemists looking to gain hands-on experience with industry-standard techniques like HPLC and GC, while building a foundation for advancement into Quality, Analytical Development, or specialized lab roles. You’ll begin with a structured weekday training program before transitioning to a weekend-focused schedule (Friday–Monday)—giving you three days off each week while contributing to critical lab operations. What You’ll Do • Perform analytical testing using techniques such as HPLC, GC, UV-Vis, FTIR, titration, and wet chemistry, • Prepare samples through dilution, filtration, centrifugation, and other methods, • Ensure accuracy by running quality control samples and verifying results, • Document and report data with precision using laboratory systems and logs, • Support laboratory operations, including instrument calibration and maintenance, • Maintain compliance with GMP standards and safety protocols, • Collaborate with a team of scientists to troubleshoot and resolve analytical challengesWhat You Bring, • Bachelor’s degree in Chemistry (required) or related science field, • 0–2 years of lab experience (internships, academic labs welcome!), • Exposure to HPLC or GC techniques (academic or industry), • Familiarity with wet chemistry and sample preparation techniques, • Strong attention to detail and analytical thinking skills, • Willingness to learn and thrive in a regulated (GMP) environmentNice to Have, • Experience with GC-MS, FTIR, UV-Vis, or similar instrumentation, • Prior work in a pharmaceutical or QC lab environment, • Interest in growing within Quality or Analytical Development functionsWhy Join Us?, • Hands-on training with advanced analytical technologies, • Clear path for career growth and advancement, • Work with a collaborative, supportive lab team, • Gain experience in a regulated pharmaceutical environment, • Enjoy a 4-day workweek with 3 days offSchedule, • Training: Monday–Friday, 8:00 AM – 4:00 PM (first ~3 months), • After training (Weekend Shift):, • Friday & Monday: 6:00 AM – 2:00 PM, • Saturday & Sunday: 6:00 AM – 6:00 PMWork Environment You’ll work in a growing QC laboratory supporting pharmaceutical testing, using modern instrumentation in a GMP-regulated setting. The role involves standing for extended periods and handling laboratory equipment, with a strong emphasis on safety, accuracy, and teamwork. Grow Your Career Here This is more than a job—it’s a launchpad. Whether you’re aiming to specialize in analytical techniques, move into Quality, or expand into research and development, this role offers the experience and mentorship to get you there. Job Type & Location This is a Contract to Hire position based out of Niles, IL. Pay and Benefits The pay range for this position is $25.00 - $27.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Niles,IL. Application Deadline This position is anticipated to close on Jun 25, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionJob Title: Chemist I – 3rd Shift Weekends (QC Laboratory) Job Description This role provides hands-on analytical support in a Quality Control laboratory, performing HPLC, GC, wet chemistry, and related testing on samples to ensure compliance with specifications and Good Manufacturing Practice (GMP) standards. The Chemist I works primarily on a 3rd shift weekend schedule after completing an initial training period on 1st shift, and plays a key role in running samples, maintaining accurate documentation, and supporting a 24/7 laboratory operation. This position offers strong growth potential into Quality or Analytical Development roles or into documentation-focused positions. Responsibilities • Log in samples or specimens by accurately recording date, time, and required tests, ensuring proper traceability and chain of custody., • Prepare samples for testing by performing appropriate dilutions, filtrations, centrifugations, digestions, and other wet chemistry sample preparation techniques., • Perform standard chemical tests using HPLC, GC, wet chemistry, UV-Vis, titration, and other analytical methods, interpreting results and correlating them with other relevant information as needed., • Run quality control samples with known values to verify that procedures and results remain within acceptable limits and take appropriate action if deviations occur., • Collect or assist in collecting samples for analysis, ensuring proper handling, labeling, and storage in accordance with laboratory procedures and GMP requirements., • Enter test results into logs, specification sheets, laboratory information systems, or other documentation tools with a high level of accuracy and completeness., • Complete test result forms and promptly notify the supervisor in cases of significant or out-of-specification findings., • Maintain accurate and up-to-date records detailing all quality control procedures used and results obtained for each test performed., • Perform routine calibration and minor preventive maintenance of laboratory equipment, including HPLC, GC, GCMS, FTIR, UV-Vis, centrifuges, and other instruments, and document all activities., • Monitor laboratory inventory, inform the supervisor of supply needs, and help ensure that reagents, standards, and consumables are available and properly stored., • Stay current in the field by reading relevant scientific literature and participating in symposiums, workshops, or other professional development activities as appropriate., • Maintain knowledge of and compliance with GMP operations, laboratory policies, and standard operating procedures., • Apply logical and scientific thinking to troubleshoot analytical issues and solve a wide range of practical and technical problems in the laboratory., • Interpret and work with nonverbal scientific information, such as formulas, scientific equations, graphs, and other data representations., • Write clear and concise reports, business correspondence, and procedure documentation as required., • Effectively present information and respond to questions from colleagues, managers, clients, and other stakeholders., • Follow all safety procedures, including proper handling of chemicals, use of personal protective equipment, and adherence to laboratory safety protocols., • Stand for extended periods and perform manual tasks such as handling, reaching, and manipulating laboratory tools, equipment, and samples., • Lift and move materials and equipment weighing up to 50 pounds as needed to support laboratory operations.Essential Skills, • Bachelor’s degree (BS) in Chemistry or a closely related science field from a four-year college or university, or an equivalent combination of education and experience., • Chemistry degree is required; candidates may be recent graduates or have 0–2 years of laboratory experience., • At least 1 year of HPLC or GC (gas chromatography) experience from school or industry is preferred; industry experience with HPLC and analytical laboratory work is strongly valued., • Hands-on experience with wet chemistry techniques and sample preparation, including dilution, filtration, centrifugation, and digestion., • Familiarity with GMP (Good Manufacturing Practice) operations in a laboratory or pharmaceutical environment., • Experience working with HPLC, GC, GCMS, FTIR, UV-Vis, and other chromatography and spectroscopic techniques, or a strong foundation to learn these methods., • Proficiency with Microsoft Office applications and ability to maintain electronic and paper-based laboratory documentation., • Strong ability to read, analyze, and interpret professional journals, technical procedures, governmental regulations, and other scientific or business materials., • Ability to write clear reports, business correspondence, and procedure manuals., • Ability to effectively present information and respond to questions from managers, clients, customers, and other groups., • Demonstrated ability to apply principles of logical and scientific thinking to solve a wide range of intellectual and practical problems., • Ability to work with nonverbal symbolism such as scientific formulas, equations, graphs, and other complex data representations., • Ability to manage multiple tasks in a fast-paced QC laboratory environment while maintaining accuracy and compliance., • Physical ability to stand frequently, use hands to handle or feel objects, tools, or controls, reach with hands and arms, and regularly lift and/or move up to 10 pounds and frequently lift and/or move up to 50 pounds., • Specific vision abilities including close vision, color vision, depth perception, and the ability to adjust focus, as required for detailed laboratory work.Additional Skills & Qualifications, • Entry-level candidates with a Chemistry degree and 0–2 years of laboratory experience are encouraged to apply., • Industry experience in a pharmaceutical or GMP-regulated environment is highly beneficial., • Experience performing titrations, UV-Vis analysis, and other wet chemistry techniques., • Familiarity with chromatography and mass spectrometry techniques, including HPLC, GC, GCMS, and FTIR., • Experience with preventive maintenance and calibration of laboratory equipment., • Strong attention to detail and commitment to maintaining accurate, compliant documentation., • Interest in career growth into Quality, Analytical Development, or documentation-focused roles., • Willingness to work a 3rd shift weekend schedule after completion of training., • Ability to adapt to a growing, 24/7 laboratory operation and support changing project and customer needs.Work Environment This position is based in a Quality Control (QC) laboratory environment that supports a growing portfolio of customer projects and is transitioning to 24/7 operations. The QC lab team consists of approximately 20–25 people, providing a collaborative setting where chemists work together across shifts to meet testing and project timelines. The role involves extensive hands-on benchwork using HPLC, GC, GCMS, FTIR, UV-Vis, centrifuges, and other analytical and wet chemistry equipment. Work is performed under GMP conditions with a strong focus on quality, documentation, and regulatory compliance. The standard schedule for this role is a 3rd shift weekend rotation: Friday, Saturday, Sunday, and Monday. Training is conducted on 1st shift for approximately three months, Monday through Friday from 8:00 a.m. to 4:00 p.m. After training, the regular schedule consists of four working days followed by three days off, with hours typically Friday 6:00 p.m.–2:00 a.m., Saturday and Sunday 6:00 p.m.–6:00 a.m., and Monday 6:00 p.m.–2:00 a.m. The position requires frequent standing, manual handling of laboratory tools and samples, and the ability to lift and move materials up to 50 pounds. Appropriate laboratory attire and personal protective equipment are required at all times to ensure safety and compliance. Job Type & Location This is a Contract to Hire position based out of Morton Grove, IL. Pay and Benefits The pay range for this position is $25.00 - $27.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Morton Grove,IL. Application Deadline This position is anticipated to close on Jun 27, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionPOSITION SUMMARY Reporting to the Manager of R&D, this position is responsible for formulating, testing, and reverse engineering personal care products that are safe, cost-effective, and manufacturable. Responsibilities Maintain a working knowledge of basic laboratory equipment. Formulate cosmetic products, including original formulations and NBE (Near-Brand Equivalent) products. Maintain a clean and orderly workstation. Interpret test results, including microbiological, stability, and challenge testing. Understand product costing and pricing requirements and formulate to meet those targets. Stay current on emerging technologies and ingredients that may present opportunities for the company and its customers. Interface regularly with customers to ensure laboratory deliverables meet expectations. Interface regularly with chemical vendors to ensure all required materials are available to complete assignments. Maintain a working knowledge of all Sigan America policies, procedures, and testing requirements. Uphold and model company cultural values of dignity and respect. Perform other duties as assigned by the Manager of R&D. Occupational Requirements Qualifications / Certifications Bachelor of Science degree in Chemistry, Biology, or a related scientific discipline. 1–3 years of experience in an R&D laboratory environment. Alternatively, 3–5 years of R&D laboratory experience without a degree. Skills / Knowledge Strong verbal and written communication skills. Strong interpersonal skills, with the ability to collaborate effectively across departments and with customers. Strong analytical and problem-solving abilities. Ability to manage changing priorities in a fast-paced environment. Strong report-writing skills. Ability to work independently with minimal supervision on complex projects.

Job Description If you've spent years formulating UV inks and coatings and you're ready to take on more ownership, this is the role where your bench work actually moves markets. Pave Talent is hiring on behalf of our client, one of North America's top three ink manufacturers, a $1B+ global company with R&D facilities and production operations across the US, Europe, and South America. Their UV liquid division supports flexible packaging, commercial printing, and digital applications at scale. This is a full-time, onsite role based in West Chicago, Illinois. ⠀ ???????????? ???????????????? ???????????????? ???????????????????????? ???????????? The R&D team here is one of the most experienced ink chemistry groups in the industry. One in three chemists on this team has over 15 years of experience. That means you're not walking into a training ground; you're joining a knowledge-dense group that will challenge you technically from day one. You'll have room to own projects from ideation through customer delivery. The hiring manager described it clearly: they want someone who can take a project and run with it, not someone who needs direction at every step. If that's how you work best, this is your environment. ⠀ ???????????? ???????????????????????????????????????????? You'll join the UV Liquid R&D team at a state-of-the-art R&D center in West Chicago. The team operates collaboratively but with a high degree of individual autonomy. You'll work directly with manufacturing, sales, and customers, giving you visibility across the full product lifecycle, not just the lab. This role is part of a business unit experiencing significant growth in flexible packaging, which means new project work is constant and your contributions will have direct commercial impact. ⠀ ???????????????? ????????????'???????? ???????????????????? • Develop new UV Flexographic and UV Screen Ink technologies based on evolving customer needs and market trends, • Handle EB Liquid formulation projects and UV/EB Coatings development for packaging applications, • Troubleshoot technical issues with existing UV ink technologies and provide direct customer support, • Evaluate raw materials and optimize formulations to identify cost-savings opportunities, • Conduct analytical testing using GC, GC/MS, FTIR, Karl Fischer, and related instrumentation, • Provide technical support to manufacturing during scale-up and production runs, • Publish project reports and technical documents directly to sales teams and customers, • Maintain lab equipment and ensure accurate documentation in SAP and related systems ⠀ ???????????????????????????????????????????????????????? ????????????????????????????????: • Bachelor's degree in Chemistry or closely related field, • 5+ years of hands-on formulation experience in inks, coatings, or a closely related field, • Direct experience with UV/EB curable chemistries, UV Flexo, or UV Screen inks, • Solid understanding of photopolymerization, resin chemistry, pigment dispersions, and rheology, • Strong communication skills with the ability to work directly with customers and manufacturing teams ???????????????????? ????????????????????????: • Background from ink industry companies (Sun Chemical, Flint Group, Siegwerk, Toyo Ink, or similar), • Experience with paint or industrial coatings and an interest in transitioning into inks, • SAP experience, • Low migration or food-contact ink expertise, • Customer-facing or technical service experience alongside bench work ⠀ ???????????????????????????????????????????????? ???????????? ???????????????????????????????? ???????????????? ????????????????????????: Competitive (commensurate with experience) ????????????????????????????????: Full-time, onsite, West Chicago, IL ????????????????????????????????: Medical, dental, vision, life insurance, disability, pet insurance, HSA and FSA ????????????????????????????????????????: 401(k) ????????????: Paid Volunteer Time Off and Paid Parental Leave included ????????????????????????????????: New office space and new lab equipment at a state-of-the-art R&D center ????????????????????????????????????: Average employee tenure of 12 years; this is a company people stay at ⠀ Interested? Apply via LinkedIn and we'll be in touch. Confidential search; your application is fully private. ???????????????? ???????????????????????? | ???????????????????????? ????????????????????????????????????????

Job Description Job Title: QC Chemist – 1st Shift Weekends Job Description This QC Chemist role oversees weekend first-shift quality control laboratory operations, providing analytical support for routine processes and new products in a regulated GMP environment. The position carries responsibility for managing laboratory activities during the shift, ensuring accurate testing of raw materials, intermediates, in-process controls, stability, and cleaning samples, and maintaining full compliance with quality, health, safety, environmental, and data integrity standards. Responsibilities • Accept responsibility for overall laboratory management and decision-making during the assigned weekend shift., • Provide analytical support for routine manufacturing processes and the introduction of new products., • Manage the maintenance and calibration of laboratory equipment to ensure reliable performance and data accuracy., • Oversee documentation and traceability of raw materials, intermediates, in-process controls (IPCs), stability, and cleaning samples., • Review existing standard operating procedures (SOPs) and standard operating procedure qualifications (SOPQs) and write new SOPs and SOPQs as required for new equipment, technology, or processes., • Participate in the description and optimization of technical procedures and analytical methods, including method review and updates., • Initiate and manage change controls related to documentation, systems, and quality control laboratory reports., • Support the introduction and implementation of new work procedures and analytical practices in the laboratory., • Approve or reject raw materials, intermediates, IPCs, stability samples, and cleaning samples in accordance with current specifications and SOPs., • Create and complete analytical records according to current SOPs and SOPQs to support material and product approval or rejection., • Maintain order, cleanliness, and good laboratory practices within the QC laboratory., • Enter analytical data and calculations into the appropriate systems, ensuring accuracy, completeness, and compliance with data integrity principles., • Generate, review, and print analytical records, bulletins, and related documentation as required., • Control and manage the sample library, including proper storage, tracking, and retrieval of samples., • Write and investigate laboratory deviations, out-of-specification (OOS), out-of-trend (OOT), out-of-expectation (OOE) results, and other laboratory events, documenting findings and corrective actions., • Promote and comply with Health, Safety and Environment procedures, quality standards, GMP requirements, and Data Integrity principles after receiving appropriate training., • Support continuous improvement by identifying, defining, and implementing initiatives that increase efficiency and optimize the use of laboratory resources., • Collaborate with laboratory management and, over time, provide guidance and direction to other analysts working on the same shift. Essential Skills • Minimum of 3+ years of hands-on chemistry laboratory experience in a GMP-regulated environment such as pharmaceutical, medical device, food, chemical, or related industries., • Strong experience in analytical chemistry and wet chemistry techniques., • Practical experience with high-performance liquid chromatography (HPLC) in a QC or analytical lab setting., • Experience working under Good Manufacturing Practice (GMP) regulations and quality systems., • Ability to perform testing and data review for raw materials, intermediates, in-process controls (IPCs), stability samples, and cleaning samples., • Working knowledge of gas chromatography (GC) and related chromatographic techniques., • Understanding and practical application of data integrity principles, including ALCOA and ALCOA+ standards., • Experience conducting data review, including audit trail review, to ensure completeness, consistency, and accuracy of analytical results., • Ability to write, follow, and revise SOPs, SOPQs, analytical records, and technical documentation., • Proficiency with Microsoft Office tools, particularly Excel and Word, for data handling and documentation., • Ability to investigate and document deviations, OOS, OOT, OOE, and other laboratory events in a structured, compliant manner., • Degree in a scientific discipline, with Chemistry or Pharmacy strongly preferred., • Training or familiarity with Health, Safety & Environment requirements in a laboratory setting., • Ability to manage multiple tasks, prioritize workload, and maintain attention to detail in a fast-paced QC environment., • Strong written and verbal communication skills for clear documentation and collaboration with cross-functional teams. Additional Skills & Qualifications • Experience in pharmaceutical or medical device QC laboratories is highly beneficial., • Hands-on experience with gas chromatography (GC) and high-resolution gas chromatography (HRGC)., • Familiarity with mass spectrometry and FTIR as part of analytical workflows., • Experience using chromatography data systems such as Empower, Chromeleon, and Agilent platforms., • Prior involvement in approvals and rejections of raw materials, intermediates, IPCs, and stability samples., • Experience with audit trail review and advanced data integrity assessments in electronic systems., • Training on advanced analytical techniques such as HPLC, HRGC, GC, mass spectrometry, FTIR, and related methods., • Comfort working with both pharmaceutical and medical device products within a CDMO-style or multi-client environment., • Interest in career growth within a growing organization with expanding project portfolios., • Ability to contribute to continuous improvement initiatives and process optimization in the laboratory. Work Environment This role is based in a QC laboratory on a dedicated 1st shift weekend schedule. The regular work pattern after training consists of four days on and three days off: Friday from 6:00 a.m. to 2:00 p.m., Saturday and Sunday from 6:00 a.m. to 6:00 p.m., and Monday from 6:00 a.m. to 2:00 p.m. Initial training lasts approximately three months on a standard first-shift Monday–Friday schedule from 8:00 a.m. to 4:00 p.m. The laboratory operates under GMP conditions and uses a range of analytical technologies, including wet chemistry, HPLC, gas chromatography, mass spectrometry, FTIR, and chromatography data systems such as Empower, Chromeleon, and Agilent software. The environment emphasizes strong quality culture, data integrity, and adherence to Health, Safety and Environment procedures. Over time, the QC Chemist will serve as the more experienced professional on the weekend shift and may have two analysts working under their direction. The organization offers opportunities for advancement as new projects and client work are integrated into the site, and the weekend shift carries an additional shift differential once the role converts from contract to a permanent position. Job Type & Location This is a Contract to Hire position based out of Morton Grove, IL. Pay and Benefits The pay range for this position is $34.00 - $38.50/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Morton Grove,IL. Application Deadline This position is anticipated to close on Jun 30, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Job Title: Quality Control Chemist 2 Department: Quality Control Reports To: Quality Control Supervisor Company Summary Dental Technologies, Inc. is a company specializing in the research, formulation, compounding and packaging of dental, orthodontic and oral pharmaceutical products. Our products include dental restoratives, core build-ups, bonding agents, orthodontic adhesives, prophylaxis paste, fluoride treatments, toothpastes, rinses, and varnishes. Dental Technologies maintains a quality system according to ISO 13485, FDA and MDR standards. Dental Technologies, Inc. is dedicated to excellence in research & development, manufacturing, in-depth testing, efficient packaging, and personalized service. We are committed to the highest level of integrity, quality, and service. Essential Duties and Responsibilities • Performs all required testing on drug products, cosmetics and medical devices according to product specifications, • Properly documents all calculations and results in a laboratory notebook as well as the company electronic laboratory testing database., • Communicates with production planners and compounders regarding statuses of incoming samples and ongoing testing., • Willingness to cross train to perform other roles within the lab and assist coworkers with testing as needed., • Applies sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues. Participates in OOS investigations by providing data and supporting testing needs., • Writes Laboratory Investigation Reports (LIR) as required., • Identifies procedures that need to be updated and updates them with support as needed., • Performs basic troubleshooting of laboratory issues or quality issues in production, • Maintains a neat and orderly working environment., • Completes all training required per the Training Matrix for Quality Control Chemist 2., • Performs other tasks, as assigned. Required Qualifications • Bachelor of Sciencein Chemistry or related science and atleast 2 years of applicable laboratory experience, • Experience with wet chemistry techniques (including making standard solutions, titrations, using pH or other electrodes, etc.), • Experience with advanced laboratory techniques including analytical instrumentation (including at a minimum, HPLC, GC, and FTIR),, • Ability toapply concepts of basic algebra and geometryto lab related calculations, • Excellent attention to detail and organizational skills, • Multitasks, prioritizes, and meets deadlines intimelymanner, • Ability to work within a team and as an individual contributor in a fast-paced, changing environment Preferred Qualifications • Experience in a GLP/GMP environment inanFDA regulated manufacturing facility, • Familiarity with Out of Specification (OOS) investigationseither in a supporting capacity or writing capacity Pay Range The QC Chemist 2 is a non-exempt position that is paid hourly. Pay rate will be dependent on a number of factors including but not limited to knowledge, skills, and experience. EEO Statement Dental Technologies Inc. is proud to be an equal opportunity employer. Other Duties Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

Job Description Job Title: R&D Chemist Job Description This role focuses on supporting research and development and quality control activities within a chemical manufacturing environment. The R&D Chemist performs analytical testing on production batches and raw materials, supports manufacturing by adjusting formulations, manages laboratory documentation, and ensures products meet established specifications and customer requirements. The position offers hands-on training, exposure to a variety of products, and opportunities for long-term career growth in a collaborative, process-driven environment. Responsibilities • Perform analytical testing on production batches, raw materials, and competitive products using methods such as pH measurement, viscosity, density, solids content, titrations, and flash point determination., • Conduct basic analytical and wet chemistry tests to verify that products meet established quality and performance specifications., • Manage and maintain the database for samples, production retains, and production documentation to ensure accurate records and traceability., • Provide technical support to manufacturing processes by giving guidance on adjusting batch formulations when batches fall outside product specifications., • Prepare certificates of analysis for customers upon request, ensuring accuracy and completeness of reported data., • Calibrate, operate, and maintain laboratory instruments and operations equipment according to known standards and documented procedures., • Prepare sample batches for customers and the sales team, ensuring they are produced, labeled, and documented correctly., • Perform stability testing on laboratory and manufacturing samples to assess product performance over time., • Communicate with outside laboratories to coordinate and manage external testing when required., • Serve as a resource for confirming correct product labels and ensuring that product information is accurate and compliant with internal standards., • Read and interpret safety rules, operating and maintenance instructions, and procedure manuals, and apply this knowledge to daily laboratory activities., • Write routine reports and correspondence to document test results, observations, and recommendations., • Apply mathematical skills to calculate figures and amounts such as discounts, interest, commissions, proportions, percentages, area, circumference, volume, and basic algebra and geometry as needed for formulation and analysis., • Work in a proactive, process-driven manner, maintaining high attention to detail and organized documentation., • Collaborate effectively with a small laboratory team, sharing information and supporting continuous improvement in quality control and R&D processes. Qualifications • Bachelor’s degree with an emphasis in Chemistry or related, • Laboratory experience focused in chemistry or quality control., • At least 1 year of R&D or formulation experience in a chemical or food manufacturing company., • Hands-on experience with wet chemistry techniques, including titration and basic analytical tests.Job Type & Location This is a Contract to Hire position based out of Countryside, IL. Pay and Benefits The pay range for this position is $25.00 - $26.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Countryside,IL. Application Deadline This position is anticipated to close on Jun 23, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Job Title: R&D Chemist Job Description This role focuses on supporting research and development and quality control activities within a chemical manufacturing environment. The R&D Chemist performs analytical testing on production batches and raw materials, supports manufacturing by adjusting formulations, manages laboratory documentation, and ensures products meet established specifications and customer requirements. The position offers hands-on training, exposure to a variety of products, and opportunities for long-term career growth in a collaborative, process-driven environment. Responsibilities • Perform analytical testing on production batches, raw materials, and competitive products using methods such as pH measurement, viscosity, density, solids content, titrations, and flash point determination., • Conduct basic analytical and wet chemistry tests to verify that products meet established quality and performance specifications., • Manage and maintain the database for samples, production retains, and production documentation to ensure accurate records and traceability., • Provide technical support to manufacturing processes by giving guidance on adjusting batch formulations when batches fall outside product specifications., • Prepare certificates of analysis for customers upon request, ensuring accuracy and completeness of reported data., • Calibrate, operate, and maintain laboratory instruments and operations equipment according to known standards and documented procedures., • Prepare sample batches for customers and the sales team, ensuring they are produced, labeled, and documented correctly., • Perform stability testing on laboratory and manufacturing samples to assess product performance over time., • Communicate with outside laboratories to coordinate and manage external testing when required., • Serve as a resource for confirming correct product labels and ensuring that product information is accurate and compliant with internal standards., • Read and interpret safety rules, operating and maintenance instructions, and procedure manuals, and apply this knowledge to daily laboratory activities., • Write routine reports and correspondence to document test results, observations, and recommendations., • Apply mathematical skills to calculate figures and amounts such as discounts, interest, commissions, proportions, percentages, area, circumference, volume, and basic algebra and geometry as needed for formulation and analysis., • Work in a proactive, process-driven manner, maintaining high attention to detail and organized documentation., • Collaborate effectively with a small laboratory team, sharing information and supporting continuous improvement in quality control and R&D processes. Qualifications • Bachelor’s degree with an emphasis in Chemistry or related, • Laboratory experience focused in chemistry or quality control., • At least 1 year of R&D or formulation experience in a chemical or food manufacturing company., • Hands-on experience with wet chemistry techniques, including titration and basic analytical tests.Job Type & Location This is a Contract to Hire position based out of Countryside, IL. Pay and Benefits The pay range for this position is $25.00 - $26.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Countryside,IL. Application Deadline This position is anticipated to close on Jun 23, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionJob Title: Chemist III Job Description The Chemist III is responsible for the coordination and organization of stability or reference standard studies to ensure seamless daily operations related to procurement, dispensing, studying, analyzing, and reporting of these studies. The role requires ensuring compliance with Stability and Reference Standard Operations while interfacing with cross-functional teams to request samples, resolve issues, and implement new studies. Responsibilities • Provide timely stability services to ensure required studies are initiated in alignment with filing strategies and business needs., • Ensure stability protocols are written, materials are obtained, and samples are placed into chambers on time., • Revise studies as needed to prevent interruptions or protocol deviations., • Load, review, and verify static tables to ensure data accuracy., • Review, analyze, and trend data to identify potential negative or aberrant results., • Communicate findings with management, quality, and laboratory teams., • Initiate exception reports as needed., • Compile clear and concise graphical and tabular summaries of data., • Author, review, and approve change control documentation., • Develop and write reports, including verification of study results and findings., • Coordinate across internal systems (including LIMS platforms) to ensure accurate tracking and reporting of study data.Essential Skills, • Minimum 5+ years of experience in a laboratory-based role with a strong emphasis on data analysis., • Experience working in QC or R&D laboratory environments, such as stability or analytical testing., • Hands-on experience with laboratory techniques such as HPLC or similar analytical methods., • Familiarity with LIMS systems.Additional Skills & Qualifications, • Strong data analysis and interpretation skills., • Ability to work independently and manage multiple tasks., • Proven track record of meeting deadlines in a structured, fast-paced environment., • Strong attention to detail with the ability to ensure accuracy in reporting and documentation., • Effective communication skills to collaborate across cross-functional teams.Work Environment This position is primarily office-based with a focus on data analysis, reporting, and study coordination. The role involves limited hands-on laboratory work. Job Type & Location This is a Contract position based out of North Chicago, IL. Pay and Benefits The pay range for this position is $40.00 - $45.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in North Chicago,IL. Application Deadline This position is anticipated to close on Jun 30, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionCompany Description Veolia in North America is the top-ranked environmental company in the United States for three consecutive years, and the country’s largest private water operator and technology provider as well as hazardous waste and pollution treatment leader. It offers a full spectrum of water, waste, and energy management services, including water and wastewater treatment, commercial and hazardous waste collection and disposal, energy consulting and resource recovery. Veolia helps commercial, industrial, healthcare, higher education and municipality customers throughout North America. Headquartered in Boston, Veolia has more than 10,000 employees working at more than 350 locations across North America. Job Description Union: Yes Schedule: 8 hour shift Ability to commute/relocate: Sauget, IL 62201: Reliably commute or planning to relocate before starting work (Required) Work Location: In person Position Purpose: Perform testing of inbound and process materials to hazard class/ better manage the waste utilizing various laboratory techniques, fingerprint screens, cyanide analysis. This position is a great way to begin your career with Veolia. Veolia has several career growth opportunities within the laboratory and across Veolia. Primary Duties /Responsibilities: • Under direct supervision, responsible for performing routine tasks and simple analysis on hazardous waste samples utilizing prescribed procedures following company and regulatory guidelines and other wet chemistry methodologies to determine the nature of hazardous substances and ensure regulatory compliance. • Analysts will gain a host of experience typically in less than two years on various instruments such as gas chromatographs, calorimeters, flash point testers, ICPs, Mercury Analyzers, Ion Chromatography, pH meter, and Bomb Calorimeters. As well as site-specific training in the environmental side of waste management.Qualifications Education / Experience / Background: • Bachelor’s degree in Chemistry or a related science discipline preferred, • Prior laboratory work experience of 2-4 years required The ability to use laboratory apparatus and equipment to perform safely, accurate, reproducible work and define problems, collect data, troubleshoot and draw valid conclusions. Knowledge / Skills / Abilities: • Strong team player, • Excellent interpersonal and communication skills, • Time management: the ability to organize and manage multiple deadlines, • Strong customer orientation, • Professional attitude in communication with internal/external customer Veolia will train on the following: Hazwoper Chemical hygiene Analytical parameters Techniques SOP's Waste management Departmenta Operating Procedures Safety OSHA Instrumentation and Mintenance Reagent Standard Preparation Supply Inventory #Lab Technician, #Environmental Technician, #Technician, #Chemist, #Lab Assistant, #Lab Analyst, #Scientist, #Science Background, #Gas Chromatograph, #HPLC, #ICP, #Atomic Absorbance, #Chemistry / Biology / Environmental Additional Information Targeted Hourly Pay: $27.58 Benefits: Our employees are covered by comprehensive benefits packages including paid time off policies; health, dental, vision, and life insurance; retirement plans, savings accounts; tuition reimbursement; paid volunteering and more. We are 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, disability or protected veteran status. Disclaimer: The salary, other compensation, and benefits information is accurate as of the date of this posting. The Company reserves the right to modify this information at any time, subject to applicable law.

Job Description 2025 was a Record Sales Year. And 2026 is off to a great start. A new opening: Technical Sales Territory Manager for a Chicago, Illinois territory. Sell boiler and cooling tower industrial water treatment chemicals with unlimited commission potential. Work out of your home anywhere in the greater Chicagoland area. Garratt-Callahan is a profitable and private nationwide water treatment chemical company that promotes from within. We are one of the largest private water treatment companies in the U.S. We are stable, and well respected in our industry. G-C is expanding nationwide in 2026 and we are looking for aggressive, smart, educated, and promotable Technical Sales Territory Managers to join our sales team. We offer training, technical support, and an unlimited no-cap flat rate commission. Sell water treatment boiler and cooling tower chemicals to a variety of industrial customers. Maintain the existing customer base and make cold calls to develop new business. Work alongside friendly, veteran salespeople. This is an established territory with a sizeable book of business. It includes customers in Healthcare, Food & Beverage, Manufacturing, Commercial & Institutional, and Wastewater. Run chemical tests to analyze water and document results. Interact and fix mechanical equipment such as pumps, tubing, piping and valves. Program electronic equipment such as cooling tower chemical controllers. Military and mechanical backgrounds are helpful. Garratt-Callahan is proud to offer: • Compensation is based upon experience and the ability to succeed., • $90,000 to $120,000+ first year for a qualified candidate., • Great benefits including a corporate 401k, health, dental, vision, and life insurance., • Industry competitive no cap flat rate commission. And we have not changed our commission plan in 25 years. Our top Territory Sales Managers make six figure commissions. Yes, you read that right. Unlimited commission, no cap., • Expenses, and a Car Allowance of $675 per month., • Technical Support and Ongoing Training., • Stability and peace of mind. No layoffs in our 120-year history. Debt free, profitable, and growing. To Apply, please log on to: https://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=16ed56fa-3af7-47fc-878a-c4d47df49e2f&ccId=19000101000001&jobId=558876&source=CC2&lang=enUS Garratt-Callahan is an EEO/AAE employer. Minorities, women, veterans, and individuals with disabilities are encouraged to apply. You may live anywhere within the greater Chicago area. Thank you for considering the Garratt-Callahan Company. We also have multiple sales openings nationwide. Please visit the career section of our website: www.garrattcallahan.com You must have at least a four year technical degree to qualify for this position. Advanced degrees preferred. Military equivalent, such as Navy Nuclear Propulsion, or Army CBRN School, is also great. Requirements: You will be a successful applicant if you have a technical degree such as Chemistry, Chemical Engineering, Environmental Science, Biology or Mechanical Engineering. A minimum of 3 years technical sales related to water treatment chemicals is required. Selling to a variety of industrial customers is preferred. CWT is preferred. Knowledge of the Chicago industrial marketplace is preferred. NOTE: Garratt-Callahan does not sponsor work visas. No recruiters please. If you have a disability, and need assistance during the application and selection process as a result, please contact the Garratt-Callahan Human Resources department at 650.697.5811. Arrangements can be made to provide an accommodation in order to assist you in applying for an open position using our on-line system, completing any other related paperwork, interviewing, or any other portion of the employment process. This phone line is only for disability assistance. When requesting an accommodation, please provide your name, phone, email address, or any other means of contacting you. Provide a brief description of the nature of the requested accommodation. A member of the Human Resources team will then contact you to discuss your request. A request for an accommodation will not affect your opportunities for employment with Garratt-Callahan. Garratt-Callahan values differing experiences, backgrounds and perspectives among our employees, and see them as a competitive advantage. Garratt-Callahan is committed to the fair and equal treatment of all associates and applicants. Garratt-Callahan is an equal opportunity employer that evaluates qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or any other characteristic protected by law. • The “Equal Employment Opportunity is the Law” poster is available at: http://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf • Garratt-Callahan Company’s reaffirmation of Equal Employment/Affirmative Action Statement http://www.g-c.com/documents/humanresources/EEOLetterJeffGarratt.pdf Key Words: Chemistry, chemicals, scientific, science, salesperson, salesman, saleswoman, outside sales, technical sales, account representative, account executive, territory sales, territory manager, district sales, district manager, field engineer, field service, AE, sales engineer, chemical engineer, chemist, mechanical engineer, biologist, biology, microbiology, nalco, ecolab, us water, ge water, chemtreat, drew industrial, solenis, chem-aqua, suez, water treatment, boilers, cooling towers, waste water, pumps, equipment, chillers, polymers, biocides. Chicago, Joliet, Aurora, Naperville, Des Plaines, Elgin, DeKalb, Highland Park, Chicagoland.

Job Description Full time Analytical Chemist openings in Vernon Hills, IL 60061 with a major bio-pharmaceutical company! Starting ASAP!! Apply now to Chris Meyer with A-Line! Analytical Chemist PAY RATE: $35.79 per hour Analytical Chemist HOURS: Monday – Friday 8:00AM – 5:00PM Location: Vernon Hills, IL 60061 Analytical Chemist Job Summary: Provide chemistry support and/or remediation to all chemistry-related projects for medical device products currently on the market as well as participating in the conduct of the stability testing program to support the approval of process and/or product design changes. As needed, this position also supports the development and validation of analytical methodologies for incoming raw materials, in-process, and finished product release testing. Analytical Chemist Job Responsibilities: · Chemistry testing · Data review and entry · Protocol/report generation · Laboratory maintenance and support. Analytical Chemist Requirements: · BS/MS in Chemistry or related discipline with related science experience · 2-4 years of experience in pharmaceutical analytical chemistry is essential. · Hands-on experience with wet-chemistry and instrumental techniques (i.e. pH, tritration, UV-Vis, GC, HPLC). · Experience in working within an FDA regulated environment and GMP documentation requirements. · Demonstrates developed knowledge of respective scientific discipline and standard scientific method and techniques. · Excellent scientific writing skills. · Ability to multi-task various activities. · Troubleshoot issues that arise and solve problems. · Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. · Ability to discuss scientific strategies/results and interact with other functional areas, including Regulatory, Manufacturing, and Quality. · Previous experience with writing scientific protocols and reports. Why Apply: • Full benefits available after 90 days: Medical, Dental, Vision, Life, Short-term Disability, • GREAT Hours!, • Competitive Pay Rate! If you think this Analytical Chemist position is a good fit for you, please reach out to me - feel free to call, e-mail, or apply to this posting! Apply to Chris Meyer

Job DescriptionAnalytical Chemist Title: Analytical Chemist Location: Chicago, IL (on-site) Reports to: Director Laboratory Operations Full-time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials. Our Chicago, IL site provides toxicology testing and research laboratory services and specialized pre-clinical studies in support of pharmaceutical and biotechnology products. Position/Job Summary: The individual in this position is involved in studies that evaluate the safety and/or toxicity of various materials (e.g., pharmaceuticals, chemicals, etc.). This position involves formulating, developing and validating methodologies for dose formulation analysis. As needed, the Analytical Chemist supervises support personnel and reports to the Director of Laboratory Operations. This is a full-time on‑site position at our Chicago facility with no provisions for working remotely. Roles and Responsibilities: Frontage Laboratories is seeking a highly motivated and experienced Chemist/Scientist for the Dose Formulation Analysis (DFA) group supporting non-clinical toxicology studies conducted under GLP regulations. Key Responsibilities: • Develop, optimize, and validate analytical test methods for dose formulation analysis., • Preparation of formulations (e.g., solutions, suspensions, etc.) to be used in toxicology studies, • Perform analysis of dose formulation samples using HPLC/UPLC, • Analyze and interpret analytical data with high accuracy and scientific rigor, • Prepare and review Method Development/Validation and Dose Formulation Analysis (DFA) reports for GLP toxicology studies, • Function as Study Director on analytical validation studies, • Ensure compliance with GLP, SOPs, and regulatory guidelines, • Maintain analytical instruments and troubleshooting method/instrument-related issues, • Collaborate with toxicology, formulation, and study management teams to support study timelines, • Prepares SOPs and study specific methodologies, • Leads and coordinates activities of less experienced staff in specific assignments, • Interact with Study Directors and help define study priorities and schedules, • Implements and enforce the use of safety procedures, • Completes tasks within time and budget constraints, • Demonstrates the ability to contribute to the success of assignments, • Performs other duties as assigned Qualifications and Experience: • BS, MS, or PhD in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related field., • Hands-on experience with HPLC and UPLC systems., • Experience with Mass Spectrometry will be preferred., • Strong experience in analytical method development and validation., • Experience supporting Non-GLP and GLP non-clinical toxicology studies is preferred., • Excellent scientific writing and documentation skills., • Ability to work independently and in a fast-paced CRO environment., • Experience in dose formulation analysis for toxicology studies., • Familiarity with FDA, OECD, and GLP regulatory requirements., • Experience with Agilent Open Lab software. Salary: $65-80k, negotiable based on experience. Benefits: • 401k Employer Match with immediate vesting, • Vision Insurance, • Medical and Dental Insurance with multiple coverage options, • FSA (Medical, Dependent Care, and Commuter), • Short Term Disability, • Long Term Disability, • Life Insurance, • Generous Paid Holidays and PTO Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

Job DescriptionWe are seeking an innovative and driven Protein Chemist/Biochemist (Scientist / Senior Scientist) to join our dynamic R&D team. In this role, you will play a critical part in characterization of wild-type and genetically engineered fungal strains. You will work at the intersection of protein biochemistry, proteomics, and molecular biology, with a focus on optimizing protein production and implementing different protein characterization methods, utilizing data-driven insights to solve complex technical challenges and accelerate relevant projects within the Fynder group. The ideal candidate thrives in a fast-paced, collaborative startup environment and possesses deep expertise in protein purification, advanced biophysical and bioanalytical characterization, and functional assay development.Responsibilities Protein Purification & Isolation: design, develop and optimize protein purification of native and heterologously expressed proteins from complex biological matrices. Execute purification workflows utilizing automated chromatography systems (e.g., affinity, ion exchange, size exclusion, hydrophobic interaction, ÄKTA FPLC chromatography platforms). Advanced Characterization & Proteomics: Characterize the secretome and proteome of wild-type, engineered, and improved strains using biochemical, biophysical and analytical techniques, such as SDS-PAGE, western blotting, ELISA based assays, UV/vis spectroscopy, mass spectrometry, Bio-Layer Interferometry, flow cytometry, etc., to evaluate purity, structural integrity, post-translational modifications such as glycosylation, inter- and intra-molecular bonding, potency, stability, developability and functional activity. Method & Assay Development: Independently design, develop, and optimize novel analytical methods and functional assays to determine structural and biophysical and biochemical attributes (e.g., molecular weight, aggregation, and stability). High-Throughput Screening: Establish and execute high-throughput (HTP) micro-scale purification and screening workflows to rapidly evaluate large fungal variant libraries. Cross-Functional Collaboration: Work within interdisciplinary teams and partner closely with molecular biology, strain engineering and fermentation teams to improve protein expression, yield, and product quality. Genotype-to-Phenotype Discovery: Partner closely with the molecular biology team to uncover connections between genotypes and key phenotypes of filamentous fungi, actively contributing to strain engineering and improvement strategies. Execution & Data Analysis: Conduct hands-on, bench-top laboratory work, designing and troubleshooting independently, analyzing and interpreting data sets, and utilizing specialized software (e.g., Proteome Discoverer, UNIFI, PyMOL, or Prism) to deliver data-driven solutions to technical roadblocks. Reporting & Presentation: Analyze and summarize results, maintaining meticulous experimental documentation, preparing SOPs, technical reports and presentations, and present scientific outcomes clearly and concisely to stakeholders. Planning and Integration: Contribute to project planning, timelines and cross-functional scientific discussions. Position Requirements & Qualifications • MS or Ph.D in Protein Chemistry, Biochemistry, or related field, • 2+ years of industrial experienceTechnical Competencies: Deep knowledge of protein structure-function properties, advanced protein purification principles, structural characterization and understanding of protein chemistry, protein folding, aggregation and stability. Experience with biologics characterization assays, including binding, blocking, competitive binding, functional activity using biochemical and cellular systems, etc Proven hands-on expertise characterizing post-translational modifications, such as protein glycosylation profiles. Experience with analytical instrumentation, including automated chromatography systems (FPLC/ÄKTA) and mass spectrometry (LC-MS/MS or MALDI-TOF), and analytical method development. Experience working with microbial hosts and strain improvement programs focused on protein expression, metabolic engineering, or related applied research targets. Familiarity with foundational computational software tools for structural visualization, data analytics, or proteomics pipelines (e.g., PyMOL, JMP, Prism, or equivalent). Core Soft Skills & Attributes: Communication: Exceptional written, verbal, and interpersonal communication abilities required for cross-team coordination. Teamwork & Mindset: An innovative mindset, a can-do attitude, and an intrinsic enthusiasm for engineering novel biological platforms for protein production. Adaptability: Highly organized, detail-oriented, and perfectly comfortable navigating the fast-paced, shifting landscape of an early-to-mid stage biotech startup. Preferred Qualifications: Direct experience in quantifying and thoroughly structurally characterizing heterologously produced complex proteins. Specific, hands-on scientific background working directly with filamentous fungi expression platforms. Experience developing micro-scale high-throughput protein screening workflows or leveraging automated liquid handling systems. Familiarity or basic working knowledge of industrial downstream processing (DSP) operations or engineering scale-up principles. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Job DescriptionCompany Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description For the Senior Scientist I position, we are seeking a highly motivated candidate who can conceive, implement and execute novel scientific research and development, independently develop, optimize new methods and techniques to generate reliable and reproducible data in a timely manner and demonstrate broad versatile technical expertise. They will support early phase development of New Chemical Entities (NCEs), particularly synthetic peptides, in both the preclinical- and clinical-development space and collaborate within the global Analytical R&D organization and with R&D cross-functional partners such as Pre-Clinical Safety (PCS), Process Chemistry, Process Engineering, Drug Product Development (DPD), Quality Assurance (QA), and CMC-Regulatory Affairs. Experience with peptide development is required and chromatographic analysis (such as HPLC or GC) and Mass Spectrometry is highly preferred. Responsibilities • Responsible for efficiently leading and supporting new peptide product development, from an analytical perspective, while working with cross-functional areas to advance projects through the development pipeline., • Support new peptide product development with advanced analytics to drive the pipeline and impactful research initiatives., • Utilize understanding of a range of analytical techniques to conduct research and development studies related to synthetic-molecule drug substances, impurities, and impurity profiling., • Highly autonomous and productive in performing laboratory research and/or method development, requiring only minimal direction from or interaction with supervisor., • Initiate new areas of investigation that are scientifically meaningful, reliable, and can be incorporated directly into a research or development program., • Formulate conclusions and design follow-on experiments based on multidisciplinary data., • Process, interpret, and visualize data to facilitate project team decisions., • Routinely demonstrate scientific initiative and creativity in research or development activities and maintain a high level of productivity in the lab., • Responsible for method development, testing procedures, and implementation of analytical control strategies to help the advancement of drug discovery candidates., • Raises the bar and is never satisfied with the status quo.Qualifications, • Bachelors, Masters, or Ph.D. in Chemistry (Analytical/Organic/Medicinal) or Pharmaceutical Sciences typically with minimum 10 (BS), 8 (MS), or 0 - 2 (Ph.D.) years related industry experience., • Strong technical background in peptide development with excellent analytical problem-solving skills. Capable of independently developing and troubleshooting analytical methods., • Demonstrated experience with HPLC analysis and method development preferred along with expertise and fundamental understanding of spectroscopic techniques as they relate to peptide development and small molecules., • Comfortable discussing organic chemistry topics within analytical R&D and with partner functions. Hands-on experience with synthetic organic chemistry preferred., • Self-motivated, hard-working, detail-oriented individual able to work in a fast-paced team environment., • Experience in the use of computerized data handling systems., • High-quality written and oral communication skills and ability to interact effectively with interdisciplinary scientists and engineers., • Practical knowledge of organic structure, functional groups, chemistry, and modern spectroscopic techniques as applied to small-molecule analytical analysis., • Builds strong relationships with peers and cross functionally with partners outside of team to enable higher performance., • Learns fast, grasps the "essence" and can change course quickly where indicated., • Creates a learning environment, open to suggestions and experimentation for improvement., • Embraces the ideas of others, nurtures innovation and manages innovation to reality. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this roleat the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factorsincluding geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned,vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable toa particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion,consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

Job Description Analytical Chemist – QC Laboratory Stix Enterprises, LLC, Wheeling, Illinois Hourly • Part-Time or Full-Time • Flexible Schedule About Stix Stix Enterprises is a premier Midwest manufacturer of botanical oils and cannabidiol (CBD) products. Based in Wheeling, Illinois, we operate a cGMP-aligned processing facility with a focus on quality, compliance, and continuous improvement. Our team is small, collaborative, and committed to producing best-in-class products. The Role We are seeking an Analytical Chemist to lead day-to-day operations in our QC laboratory. The chemist will perform sample intake and preparation, run analyses on our Agilent HPLC and GC-MS instruments, interpret raw data, and generate certificates of analysis. There is opportunity to be trained on our Agilent Q-TOF system for advanced method development and accurate-mass work, prior Q-TOF experience is welcomed but not required. This position is structured as an hourly role and can be filled on a part-time or full-time basis. The schedule is flexible. The opportunity is well-suited to an experienced chemist including a semi-retired or returning professional who wants meaningful, hands-on lab work without the demands of a corporate career track. Key Responsibilities • Sample preparation and testing — Prepare and analyze samples (cannabinoid potency, terpenes, residual solvents, and related panels) in a timely, accurate manner., • Instrumentation — Operate and maintain Agilent HPLC and GC-MS systems, including routine tuning, calibration, column changes, and source cleaning., • Data analysis and reporting — Review and interpret chromatographic data using OpenLab and MassHunter; generate certificates of analysis and internal reports., • Method development — Develop, validate, and document analytical methods for new sample types and product formats., • Documentation and compliance — Maintain laboratory documentation in alignment with cGMP and data-integrity (ALCOA+) principles, including SOPs, logbooks, calibration records, and chain-of-custody., • Collaboration — Partner with production and operations to investigate out-of-specification results and support process improvements., • Q-TOF (training provided) — Opportunity to be trained on our Agilent Q-TOF platform for high-resolution accurate-mass work; prior experience is a plus but not required. Required Qualifications • Bachelor's degree (or equivalent experience) in chemistry, biochemistry, or a related analytical science., • Hands-on working experience with HPLC and GC-MS, including sample preparation, system suitability, and routine maintenance., • Comfort with analytical software (Agilent OpenLab and MassHunter preferred; equivalent platforms acceptable)., • Working knowledge of analytical fundamentals: calibration curves, peak integration, LOD/LOQ, internal standards, and basic method validation., • Familiarity with standard lab equipment — analytical balances, centrifuges, vortex shakers, pH meters, moisture analyzers — and safe handling of common solvents (methanol, acetone, heptane, etc.)., • Strong attention to detail, organization, and documentation discipline., • Ability to work independently, troubleshoot effectively, and communicate clearly with a small team., • Proficiency with Microsoft Excel and Word. Preferred Qualifications • Prior experience in cannabis, hemp, botanical, pharmaceutical, food, or environmental testing laboratories., • Familiarity with cGMP (21 CFR 111 / 211), ISO/IEC 17025, or USP general chapters., • Experience with method validation per ICH Q2(R1) and/or analytical method transfer., • Exposure to Q-TOF or other high-resolution mass spectrometry (we will train)., • Experience with LIMS or electronic lab notebooks. Schedule and Compensation • Hourly position, part-time or full-time, depending on candidate availability., • Flexible weekday schedule; specific hours to be agreed upon at offer., • Compensation is competitive and commensurate with experience. Physical Requirements • Ability to lift and carry up to 25–30 lbs and place items onto waist-high surfaces., • Ability to sit or stand for extended periods and to bend or crouch as needed for instrument access., • Ability to wear required PPE (lab coat, safety glasses, gloves) for the duration of the shift. Equal Opportunity Stix Enterprises, LLC is an equal opportunity employer. We welcome applicants of all backgrounds and experience levels, including returning and semi-retired professionals. Employment is contingent on the successful completion of any background checks and industry-required screenings. To apply, please submit a résumé and a brief note describing your hands-on experience with HPLC and GC-MS, and your preferred schedule (part-time or full-time). Company DescriptionLabor Solutions Professional is a leader in the professional, temporary, and direct hire industry. Our clients range from individual entrepreneurs to large corporations, and while we are big enough to serve Fortune 100 companies, we are small enough to stay nimble in an always-changing market. Thank you!Labor Solutions Professional is a leader in the professional, temporary, and direct hire industry. Our clients range from individual entrepreneurs to large corporations, and while we are big enough to serve Fortune 100 companies, we are small enough to stay nimble in an always-changing market.\r\n\r\nThank you!

Job Description Our solutions protect patients! Founded in 1932, Xttrium Laboratories, Inc. is a Family Owned and Operated Company based out of the Chicagoland area. We are committed to human health and take great pride in being a leading manufacturer and supplier of antiseptic products across the country. Xttrium Laboratories began as a small group of doctors and nurses working to treat individual patient needs. Today, our portfolio has expanded to over 150 different FDA-approved infection prevention and healthcare products. With 85 years of experience, the Xttrium Team is driven to provide solutions to a wide variety of health and safety concerns. Job Description The Chemist I within the QC Laboratory conducts routine sample analysis and preparation with and without the use of instrumentation following official methods and laboratory Standard Operating Procedures (SOPs). Builds their knowledge and skills in evaluation of the chemical and physical properties of various organic and inorganic substances for consumer product testing purposes. • Under direct supervision conducts routine analytical studies of samples and preparation with and without the use of instrumentation following official methods and laboratory Standard Operating Procedures (SOPs) and protocols., • Testing including but not limited to pH, water determination, density, titrations, viscosity, dissolution, TLC, FTIR, UV, HPLC, and GC., • Assists in preparation, submission and filing reports on sample tests, correlation tests, calibration, validation and other projects, • Performs routine operation, maintenance, calibration, and trouble-shoots laboratory instruments / equipment, • Inputs and maintains technical information as needed to support the laboratory functions/operations, • Maintains Laboratory Notebook, • Adheres to internal standards, policies and procedures, • Performs other duties as assigned Qualifications • Bachelor’s Degree in Chemistry or related Science discipline, • 0-2 years of relevant experience in one or more of the following wet chemistry techniques; assay titrations, TLC, water determination, FTIR, HPLC, GC We are proud to be an Equal Opportunity Employer. We welcome people of all backgrounds, experiences, and perspectives. Employment decisions are made based on skills, qualifications, and potential; never on race, color, religion, sex, national origin, age, disability, veteran status, or any other protected trait.

Job Description Hentzen is a unique company in today’s world. Since our inception in 1923, we have remained an independent, privately held company committed to being a leader in the development and manufacture of quality coatings through innovation, dedication and service to our customers and employees. This continual commitment has led to Hentzen’s recognition as a technology leader and trusted partner to our customers in the aerospace, defense, and industrial markets we serve. Through nearly 100 years of innovation experience, we have developed a unique ability to custom engineer advanced coatings designed to meet each of our customers’ unique and challenging requirements. This innovation comes to life in our state-of-the-art facilities where our talented employees are challenged to develop coatings to solve these unique problems. If you want to join a technology leader, known for its innovation and dedication to its customers and employees, Hentzen can offer you a rewarding and challenging opportunity to learn and grow. LAB TECHNICIAN – LIQUID R&D SUMMER INTERNSHIP 1st Shift M-F (7am – 3:30pm) The Lab Technician - Liquid R&D Intern performs small production and lab sample batch-making tasks in the production of industrial coatings products to meet customer specifications in accordance with established Hentzen Coatings health, safety, and environmental procedures under the direction of a chemist. DESCRIPTION OF ESSENTIAL DUTIES: • Gathers raw materials, assembles batches, shades, and performs QC testing., • Evaluates batches for conformance to specifications., • Adjusts properties of individual batches within formulation guidelines., • Performs testing related to product performance., • Prepares customer samples and panels., • May be required to perform all aspects of liquid batches of 10 gallons or less, such as dispersion, letdown, color matching, quality control and filling., • Maintains records of processes and results., • Documents and records all actions taken in preparation of product., • Records batch information in appropriate computer programs., • Maintains standards for housekeeping and safety., • Perform other duties as assigned. QUALIFICATION REQUIREMENTS: • Education level required: High School Diploma and pursuing 4-year degree in Chemistry, Science, or related field., • Preferred experience level: One to three years’ experience in a laboratory setting preferred and preferably in coatings, • Working knowledge of basic algebra, percentages, and a variety of measuring and testing equipment, such as Karl Fischer, scales, grind gauge, KU viscometer., • Excellent computer skills (Microsoft Office – Word, Excel, Outlook), ERP system and other office machinery, • Superb written and verbal communication skills, • Excellent color vision, • Excellent math skills including metric to standard conversions, • Works well in a team environment, • Excellent team building and communications skills 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 50 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. www.hentzen.com All candidates are subject to post-offer testing: including a job-related pre-employment physical, drug screen, and background check. M-F: 1st Shift 7:00 AM - 4:30 PM

Job Description With over 70 years of innovative products and services, Valto is the world’s leading provider of FRP composite panels. Our lightweight composite products deliver unsurpassed strength and durability; and we continue to pioneer next level performance in building materials, recreational vehicles, and transportation. We deliver quality products that perform in demanding environments. Valto is searching for a Chemist to be based out of our Joliet, IL facility. Reporting to the Technical Manager, this role focuses on performing technical project work, including raw material qualifications, identifying and implementing quality improvements, investigating product and customer issues, and developing new colors while maintaining existing color standards to meet customer needs. The individual may be responsible for presenting findings and recommendations to the Quality Coordinator, Operations, R&D, and customers. Occasional travel to customer sites may be required to investigate and resolve product quality concerns. POSITION DEMANDS: • Maintain good attendance and a positive work attitude., • Have knowledge and understanding of all safety guidelines and specific safety hazards associated with manufacturing process., • Need thorough understanding of materials (catalyst, promoter, resin, monomer, pigments, and fillers) used in process and how they are to be handled., • Must be a self-starter with strong analytical skills requiring little supervision., • Must possess an ongoing continuous improvement mind-set and possess the ability to work in a harmonious manner and interact in a cooperative way with coworkers and supervisors., • Good technical written and verbal communication skills are required, as is the ability to collaborate and be detail oriented., • Knowledge of statistical methods and the ability to apply this knowledge to resolve problems and anticipate solutions., • Must be capable of using precision measuring, weighing instruments, & color instrumentation, • Knowledge of pigments, polyester resins, and catalysts, • Have working knowledge of color measurement and control., • Have good mathematical aptitude., • Consistently demonstrate attention to details., • Have the ability to carry out long series of tests to form hypotheses or optimize mix formulation., • Ability to multi-task projects, • Must be computer literate., • Must be physically able to:, • Standing: Remaining in an upright position at workstation with moving about., • Walking: Moving about on foot, • Stooping: Bending the body downward and forward, • Climbing: Ascending or descending ladders, stairs, and scaffolding., • Handling: Seizing, holding, grasping, turning, or otherwise working with your hands., • Must be able to lift up to 60 lbs. PRINCIPAL RESPONSIBILITIES: • Assist in product qualification, test development and troubleshooting projects., • Coordinate and assist in line trials – may occur in any shift., • Determine process capability for existing and new colors., • Conduct special studies and experiments to develop new products, evaluate new test methods, evaluate new raw materials, and investigate the effect of processing factors., • Optimize existing products, evaluating test methods, raw materials and process variable., • Mix different chemicals or polymers together to discover the results and chemical properties., • Assist process engineering with trouble shooting process when raw materials are in question., • Develop and execute test plans for trial materials, alternate raw materials, and problem resolution., • Provide summary reports with supporting data and charts (Excel, Minitab), • Assist with complaint testing and investigations, along with analysis of competitor’s products., • Assist with internal non-conformances: FGH, FGR and deviations., • Assist with maintaining, updating, and revising controlled documents and forms., • Assist with updating product plans and MXVs., • Ability to utilize business system, KBM and RMS., • Able to work any shift as needed., • Perform color matching, color control, slurry formulation, special color related studies and experiments (placing emphasis on the quality of color critical raw materials, in-process & finished products)., • Maintain a clean and safe work area. Follow the established laboratory safety guidelines and procedures (including 5S)., • Assist in the continual improvement projects. Education and Experience: Bachelor of Engineering or Science (Chemistry, Biology, or Physics) or associate’s degree or equivalent experience in Chemistry. ACCOUNTABILITY: Every individual is held personally accountable for adherence to Job Safe Practice Guidelines as stated on this form and general plant rules as stated in the Employee Handbook. This position will be held accountable for the following: • Improper use of Personal Protective Equipment, • Insubordination to the supervisor/manager JOB SAFE PRACTICE GUIDELINES: Required Personal Protective Equipment: • Safety glasses with side shields, • Gloves, • Steel toed safety shoes Potential Hazards: • Many hazards associated with specific tools / machines., • Pinch points, • Moving objects, • Splash hazard producing chemical burns on/in eyes, skin, mucus membrane., • Trip hazard., • Falling objects, being hit by falling parts, or other items., • Working with exposed heights., • Exposure to dust, fumes, temperature changes, & humidity., • Hearing loss (Exposure to noisy equipment). We offer a comprehensive total rewards package that includes bonus eligibility and a competitive benefits program. This package includes employer-subsidized Medical, Dental, Vision, and Life Insurance; Short-Term and Long-Term Disability; 401(k) match, Flexible Spending Accounts, Health Savings Accounts, EAP, and Educational Assistance; Parental Leave, Paid Time Off (for vacation, personal business, sick time, and parental leave), and 11 Paid Holidays. For this role, we anticipate paying up to $75,000 per year plus bonus. Placement within the range considers experience, skills, and internal equity. Valto, Inc provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws

Job Description MOVING YOUR WORLD by focusing on your success: FUCHS offers a challenging and rewarding working environment where employees are encouraged to develop and grow. We stand behind our core values: trust, creating value, respect, reliability, and integrity. Ours is a culture that fosters creativity and empowerment, values work/life balance, and gives you the freedom to excel. At FUCHS we aim to nurture your capabilities, ideas and career. Salary: FUCHS offers a competitive salary commensurate with experience in a similar position. The salary range for this position is $64,000 - $74,000 per year, but actual salary will vary depending upon a new hire’s experience and qualifications as well as internal equity. Your Responsibilities: Within the OEM/Automotive Fluids R&D group, we develop cutting-edge lubricants for a diverse range of vehicles—from everyday passenger cars to high-performance off-road racing machines. Beyond innovation, we provide critical technical expertise to our partners in Product Management, Sales, and Quality. Reporting to the R&D Group Leader, the successful candidate will drive team success by formulating and testing next-generation automotive fluids. We are seeking a proactive, hands-on 'self-starter' who stays ahead of industry trends and fosters strong collaborative relationships across our Technical, Quality Control, and Operations departments. Qualifications we are looking for: • Master in STEM (Science, Technology, Engineering and Math) or Bachelor with a minimum of two years’ experience working in a technical role. A degree in Chemistry is preferred., • Familiar with lab procedures and testing., • Able to conduct hands-on laboratory experiments and tests in an organized and safe manner., • Likes to work in the laboratory and thrives in a dynamic and demanding environment., • Excellent record keeping and documenting skills, e.g., able to keep a well-organized lab notebook., • Strong problem solving, interpersonal, teamwork and communication skills., • Self-motivated and able to work independently., • Ability to organize and summarize results and present it to the technical group., • Must be proficient with computers and Microsoft Office programs (Word, Excel, Power Point, Outlook)., • Experience in Product development and product modifications is preferred. These are your benefits: FUCHS offers a challenging and rewarding working environment where employees are encouraged to develop and grow as professionals. In this role, you will have the opportunity to work on projects that will expand your experience and challenge your abilities in the global marketplace. The position also offers an excellent compensation package and a comprehensive suite of benefits. Detailed benefit information can be found at this link: https://fuchs.com/us/en/benefits. FUCHS Lubricants Co. is an equal employment opportunity (EEO)/AA employer and strongly supports diversity in the workplace (m/f/d/v). Do you have any questions? Rosalinda Almanza (rosalinda.almanza@fuchs.com) will be more than happy to answer them!

About Mercor’s talent network Join our Chemist Expert Network to connect with leading AI labs and companies seeking your expertise. About Mercor projects Experts in our network contribute to: - Training and evaluating AI models in Chemistry - Creating tasks and deliverables based on real-world

Chemist The Chemist is responsible for the coordination and organization of stability or reference standard studies to ensure uninterrupted daily operations associated with procurement, dispensing, studying, analyzing, and reporting of those studies while assuring compliance for Stability and Refere

AbbVie is seeking a Senior Principal Research Scientist – Process Chemistry to lead process research and development for drug conjugates, peptides, and small molecules. Candidates should have a relevant degree and significant industry experience, including a strong understanding of regulatory expe

The ideal candidate will have a BS in Chemistry or Biochemistry and strong analytical skills. Momentum Staffing Group LLC is seeking a Chemist in Bridgeview, Illinois. Responsibilities involve using GC and ICP methods, performing various wet chemistry techniques, and adhering to safety protocols whi

Position Water Chemist II – Department of Water Management, Bureau of Water Supply. Qualifications Graduation from an accredited college or university with a Bachelor’s degree or higher in Chemistry, Chemical Engineering, or a directly related field.

The ideal candidate holds a Bachelor's degree in Chemistry and has at least 2 years of laboratory experience, particularly in wet chemistry techniques and analytical instrumentation. QC Chemist 2 in Lincolnwood, Illinois.

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Primary Duties: Conduct analysis of refined productsand other samples usingGC and ICP methods Perform a variety of wet chemistry techniques Document test results and ensure accurate record keeping Follow safety protocols and attend ongoing compliance trainings Manage workload efficiently and support

The Hispanic Alliance for Career Enhancement is seeking a Water Chemist II to perform entry-level professional chemical and physical analyses of raw and treated water to ensure its quality for drinking. Candidates must hold a Bachelor’s degree in Chemistry, Chemical Engineering, or a directly rela

Chemist II Position The candidate for this Chemist II position will be working in the Drug Metabolism and Disposition group of Quantitative, Translational, and ADME Sciences (QTAS) department. BS in Chemistry or Life Sciences, 2-5 yrs.

Analytical Chemist – Afternoon Shift At Sensient Technologies, we are experts in science, art and innovation of color and flavor. We are market‑savvy and visionary. We are problem solvers. And we will be better with you. We are looking for an Analytical Chemist to join our team and be responsible for the analysis of samples and the daily operation of the QC analytical laboratory. In this role, you will organize and conduct testing of product content in compliance with applicable methods, protocols, SOPs and regulatory agency guidelines. You will also maintain documentation and laboratory records. What you’ll do: Perform accurate chemical analyses in accordance with standard methods, utilizing equipment such as gas chromatographs, spectrophotometers, density meters, turbidity meters, and other equipment in the Laboratory. Analyze samples using modern analytical instrumentation such as GC/MS, LC/MS, HPLC, FT‑IR. Maintain all analytical equipment, including troubleshooting, maintenance, and calibration to ensure minimal operational downtime, and report all malfunctions to the Quality Control Manager. Perform peer review and QC review of data. Maintain a clean and safe laboratory work environment that is compliant to GLPs and GMPs. Enter and maintain all result data in our ERP database / Excel spreadsheets and report deviations to the management team. Begin investigations behind issues. What you’ll bring: An understanding of data, including experience generating and analyzing data in a quality environment data. Experience with sample preparation, testing and using laboratory equipment. Bachelor's degree in Chemistry, Biology, or related science, or equivalent experience. Strong attention to detail and a positive attitude, the ability to work with a team. Knowledge of GMPs, GLPs, FDA, HACCP, SQF. What you’ll get: An excellent salary, benefit offering, and development opportunities to include 401(k), stock purchase plans and more. A thorough and effective training experience during onboarding and beyond. Take your career to the next level and work with amazing people around the world. An opportunity to collaborate on site full time with a terrific team. About Sensient: Sensient Technologies Corporation is a leading global manufacturer and marketer of colors, flavors, and extracts. Sensient employs advanced technologies at facilities around the world to develop specialty food and beverage systems, cosmetic and pharmaceutical systems, specialty colors, and other specialty and fine chemicals. The Company's customers include major international manufacturers representing most of the world's best‑known brands. About Sensient Flavors: Sensient Flavors offers innovative, global taste solutions and specialized flavor delivery systems that help bring life to your food and beverage products. Our leading‑edge technologies reflect our core philosophies to be dynamic and innovative and to add value to your applications. The salary range for this position is $65,000 - $85,000. Pay within the range is based on several factors, which may include, but are not limited to, education, work experience, specialized training, and labor market conditions. In addition to salary, Sensient is proud to offer a comprehensive and competitive benefits program to support the holistic well‑being of our employees and their families. THIRD PARTY AGENCY: Any unsolicited submissions received from recruitment agencies will be considered property of Sensient Technologies, and we will not be liable for any fees or obligations related to those submissions. Sensient is an Equal Opportunity Employer, headquartered in Milwaukee, Wisconsin, USA. #LI-AH1 #J-18808-Ljbffr

Overview What Nuclear Manufacturing contributes to Cardinal Health Manufacturing is responsible for cost of production and maintenance activities including process improvement, supply chain management, quality assurance, employee safety and engagement, and environmental commitment. Nuclear Manufacturing is responsible for the manufacturing of time sensitive radiopharmaceuticals in an integrity driven, highly regulated environment (i.e. FDA, NRC, DOT) to support patient treatment through disease diagnosis, staging, and monitoring. Schedule 40 hours per week Sunday night/Monday morning - Friday Typical shift is Midnight - 8:30am but must be willing to work other shifts as needed! Training will typically be from 4am - 12:30pm. Must be willing to work weekends if needed by business needs Must be able to work overnight shift as facility operates at night. Candidate must be flexible to work different shifts, schedules, holidays, days and overtime as needed. Responsibilities Manufactures radioactive isotopes (includes synthesis set up, hot cell manipulations, distribution) Conducts quality control testing of each batch (utilizing gas chromatograph, dose calibrator, multi-channel analyzer, TLC plate scanner, high pressure liquid chromatograph, analytical balance, PTS, laminar flow hood and fume hood) Performs environmental and personnel monitoring in ISO 5, ISO 7, and ISO 8 environments Works in ISO 7 cleanroom to make product vials and customer vials for use in drug production Coordinates daily production run schedule based on customer and pharmacy needs Demonstrates strong documentation practices, oral communication, and writing skills. Performs clerical and administrative tasks, including maintenance of daily production records, report preparation and maintenance records Manages SAP Inventory (includes receiving materials, properly inspecting materials for use, and maintaining proper cycle counts) Performs daily radiation safety tasks, along with general lab cleaning Ability to troubleshoot equipment issues Advanced chromatography skills Provide feedback on method development around time of Tech Transfer Communication with external innovator/sponsor Ability to lead; judgement to prioritize quickly Qualifications Bachelor?s degree in related field, or equivalent work experience preferred. Sciences preferred 2 - 3 years HPLC experience preferred Lab experience highly preferred Must be able to work overnight shift (Facility operates at night.) Prior experience in manufacturing, preferably in a controlled environment and/or regulated industry preferred Effective written and verbal English communication skills required Able to repeatedly follow detailed processing instructions Ability to manage several tasks at the same time; Ability to evaluate operating conditions and exercise sound judgment and problem solving skills. Ability to manage weight up to 75 pounds Ability to see fine particulate and differentiate colors in liquid solutions. Ability to hear, write (English), and speak (English) clearly in order to communicate in manufacturing setting. Manual dexterity required for equipment operation and occasional reach and lifting of small objects. Ability to be an effective team member. What is expected of you and others at this level Applies basic concepts, principles and technical capabilities to perform routine tasks Works on projects of limited scope and complexity Follows established procedures to resolve readily identifiable technical problems Works under direct supervision and receives detailed instructions Develops competence by performing structured work assignments Compensation and Benefits Anticipated hourly range: $30.10 per hour - $42.90 per hour Bonus eligible: No Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being. Medical, dental and vision coverage Paid time off plan Health savings account (HSA) 401k savings plan Access to wages before pay day with myFlexPay Flexible spending accounts (FSAs) Short- and long-term disability coverage Work-Life resources Paid parental leave Healthy lifestyle programs Equal Opportunity Statement Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law. #J-18808-Ljbffr

6AM City, LLC, located in Illinois, is seeking a candidate for the Analytical Development role to support commercial method development, optimization, and validation. You will lead technology transfers and deliver product control strategies based on analytical data. This position requires a BS in Chemistry or related field, and experience with protein separation techniques. Candidates must have strong multitasking abilities and familiarity with good laboratory practices. #J-18808-Ljbffr

The Flavor Chemist position is involved in the execution from concept to commercialization of assigned new product development, quality improvement, or cost optimization in savory, beverage and dairy flavors. • Creates innovative flavors for a range of food and beverage products to meet the specific requirements of our customers, • Formulation of liquid compounded flavors, spray dried flavors, flavor emulsions, and flavor extracts, • Matches samples of flavors from competitors, food products and nature with the support of our analytical team, • Ability to formulate flavors for alcoholic beverage that meet TTB guidelines and restrictions, • Serve as project leader for creative projects, as project support for application projects, • Interface with multiple cross-functional groups to execute projects, • Provide technical support to account managers on specific projects, interact with key customers, • Provide leadership and instruction to technicians and lower level professional personnel as required, • Bachelor of Science Degree in Food Science, Chemistry, or a related Applied Science required; Masters or PhD a plus, • Minimum of seven years progressive experience in the development of flavors for foods and beverages, • In depth knowledge of aroma chemicals, essential oils and other materials used in the creation of flavors, • Comprehensive knowledge of flavor regulations, flavor manufacturing procedures and US flavor regulations, • Extraordinary sense of taste and smell, ability to recognize chemicals by odor, • Interpersonal skills that allow for effective working relationships with peers, cross functional team managers and customers, • Excellent verbal and written communication skills and proficient organizational and computer skills (Microsoft Office) The actual compensation that you will be offered will depend on a variety of factors including geography, skills and abilities, education, experience and other relevant factors. This role will remain open until filled.

Company Description In a world of vibrant color, INX stands out by blending art, science, and sustainability into every drop of ink we make. We're globally recognized for our innovation, and we're A Great Place to Work-Certified company! INX International is the third largest producer of inks in North America with full-service subsidiaries in Europe and South America. We offer a complete line of ink and coating solutions technology for commercial, packaging and digital applications. We expertly blend pioneering technology with a deep commitment to the environment. Dedicated to coloring a safe and sustainable future one print at a time, you can see our color chemistry on beverage cans, food and household packaging, clothing, banners, billboards and more. Investing in and protecting our employees is the key to our success. Our average employee has been with us 12 years, and we recognize the significant experience and the continuous dedication of our team members. We're actively seeking new talent with new ideas as we continue to provide sustainable products, service and innovation to the printing and packaging markets. Join us in coloring a safe and sustainable future! Job Description This role offers a range of $84,000 to $100,000 annually. Actual compensation will be based on qualifications such as experience, education, certifications, and skills, as well as geographic considerations. We are experiencing tremendous growth in the area of flexible packaging in our solvent ink division, so we invite you to be a part of this exciting and growing team! If you are a chemist that enjoys solving problems and creating solutions in constantly growing and evolving market, this position is a great opportunity for you! Did you know that: Our R&D Dept. has a strong knowledge base. In fact,1/3of our Chemist teamhas over 15 years of experience INX has cutting-edge innovation and technology You will work in a collaborative team culture and in an autonomous workenvironment We have many opportunities for growth As a R&D Chemist you will be responsible for: Troubleshooting issues with existing technologies, as well as assisting with customer challenges Developing new UV Flexo / UV Screen Ink technologies based on customer needs Some EB Liquid work and UV/EB Coatings work as well Evaluating raw materials and optimizing formulations for cost-savings opportunities Providing technical support to manufacturing Publishing project reports and other documents direct to sales and customers Maintaining laboratory equipment Qualifications To perform your job as expected, you will be required to: Have a Bachelor's degree in Chemistry or equivalent 5 plus years of job-related experience Ink and coating formulation experience Have strong math and science skills Be a proficient recordkeeper Have good and effective written, reading comprehension and verbalskills Be able to interpret data and draw effective conclusions Additional Qualifications Knowledge of UV/EB Liquid Ink and Coatings Formulation and application experience preferred SAP experience Additional Information We offer a competitive salary with excellent benefits including medical, dental, vision, life insurance, disability, pet insurance, HSA and FSA, 401(k), and more. Through our programs, which now include Paid Volunteer Time Off and Paid Parental Leave , we support the needs of our employees, their dependents, and their communities by providing a benefit package that is easy to understand, easy to access, and affordable for all our employees. Don't just choose a job; choose a career that emphasizes employee growth in a safe, environmentally conscious culture. Embark on your Colorful Career with us! We require post-offer, pre-employment drug screens, physicals, and background checks. Equal Opportunity Employer: disability/veteran. #J-18808-Ljbffr

Job Summary Under close supervision, formulates and conducts qualitative and quantitative analysis/tests in a laboratory setting for current and or new products. Analysis contributes to process improvements, performance, and overall customer product experience. Job Description Executes, formulates and conducts qualitative and quantitative analysis/tests in a laboratory setting for current and or new products. Implements new or improved analytical test methods to enhance capabilities, efficiency and accuracy (repeatability & reproducibility). Carries out prescribed analytical tests and determinations to answer questions and address problems of customers. Records all observations and data in an orderly manner. Reports results in a clear and concise manner to enhance technical exchange. Maintains equipment, glassware and workspace to keep them clean and well-functioning. Properly disposes of all laboratory waste. Participates in ensuring good management of laboratory equipment, storage spaces for chemicals and raw materials, and compliance with housekeeping rules. Provides analytical service and knowledge to internal and external customers based on the chemist’s current level of expertise. Visits customers when required to assist the Commercial team. Ensures that all equipment and machines in your area of control are managed regarding safety, maintenance, calibration, and availability. Performs project work in cooperation with a variety of internal and external contacts. Benefits Competitive pay programs with excellent career growth trajectory Paid time off for volunteerism Dress for your day; how you dress is determined by what your day may bring Comprehensive benefit options including: Medical, Dental, Vision, Parental Leave, Holiday Pay, Paid Time Off, Tuition Reimbursement, and Savings Plan Opportunities for career growth within a global leader in industrial process fluids industry Equal Employment Opportunity 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, 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. Quaker Houghton is committed to providing reasonable accommodations to qualified candidates with physical and/or mental disabilities. #J-18808-Ljbffr

Lab/Facility Chemist IApplylocations: Harvey, IL, USAtime type: Full timeposted on: Posted Yesterdayjob requisition id: R-177131POSITION SUMMARY: The Lab/Facility Chemist performs chemical analyses of various types of hazardous and non-hazardous waste to determine compliant treatment and disposal, using a variety of analytical techniques and instruments.PRINCIPLE RESPONSIBILITIES: Performs preparation techniques and instrumental analysis of environmental samples for the determination of organic and inorganic constituents using approved EPA test methods and Standard Operating Procedures (SOP) and Work Instructions (WI). Participates in the generation of SOPs and Work Instructions (WI), under the supervision of the Laboratory Manager. Prepares samples for laboratory equipment. Utilizes and understands essential functions for instrument sequencing and data processing (performs basic instrument maintenance and repairs as needed, performs analytical standard preparations, and maintains all required documentation with accuracy and clarity). Validates methods for testing the content of organics, inorganics using a wide variety of processes and instrumentation. Performs a satisfactory Initial Demonstration of Capability (IDOC) prior to data reporting for any method the chemist will be conducting analysis. Maintains a satisfactory annual Demonstration of Capability (DOC) for each method. Identifies chemical content of materials and conducts research on appropriate treatment studies. Provides technical knowledge to help develop formulas, enhance or create processes, and methods for solution of technical problems. Maintains a clean and safe work environment. Maintains familiarity with quality control measures and calculations required for applicable methods.* Performs other related duties as assigned.PREFERRED QUALIFICATIONS: Some knowledgeable of chemistry principles and practices including analysis and evaluation, and waste processing protocols. Performing proper analysis; presenting findings in a concise format; addressing difficult situations in a constructive manner; utilizing computer technology for communication, data gathering and reporting; negotiation and problem solving. Building a rapport with associates and managers; detail oriented, with a high level of accuracy and the ability to detect inconsistencies in data. Awareness of quality management standards, including ISO and NELAC standards. Knowledge of Excel, Word, and PowerPoint applications is essential. Knowledge and understanding of RCRA, TSCA, and applicable state regulations, typically gained through less than one (1) year of progressively responsible experience in waste disposal, chemistry, or a related field.* Superior knowledge of software package as it relates to waste streams and reporting.MINIMUM QUALIFICATIONS:* A candidate with no degree would be expected to have 3 years relevant work experience.Pay Range:The pay range for this position is $27.90 to $38.32* which reflects the minimum wage in multiple jurisdictions. The actual range will depend on the locality in which you are hired.Bonus Plan Details (if applicable):Rewarding Compensation and BenefitsEligible employees can elect to participate in: • Comprehensive medical benefits coverage, dental plans and vision coverage. • Health care and dependent care spending accounts. • Short- and long-term disability. • Life insurance and accidental death & dismemberment insurance. • Employee and Family Assistance Program (EAP). • Employee discount programs. • 401(k) plan with a generous company match. • Employee Stock Purchase Plan (ESPP).• Paid Time Off (PTO)• Benefits https://jobs.republicservices.com/us/en/about-us/benefitsThe statements used herein are intended to describe the general nature and level of the work being performed by an employee in this position, and are not intended to be construed as an exhaustive list of responsibilities, duties and skills required by an incumbent so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of the Company. #J-18808-Ljbffr

*What Nuclear Manufacturing contributes to Cardinal Health* Manufacturing is responsible for cost of production and maintenance activities including process improvement, supply chain management, quality assurance, employee safety and engagement, and environmental commitment. Nuclear Manufacturing is responsible for the manufacturing of time sensitive radiopharmaceuticals in an integrity driven, highly regulated environment (i.e. FDA, NRC, DOT) to support patient treatment through disease diagnosis, staging, and monitoring.Schedule 40 hours per week Sunday night/Monday morning - Friday Typical shift is Midnight - 8:30am but must be willing to work other shifts as needed! Training will typically be from 4am - 12:30pm. Must be willing to work weekends if needed by business needs Must be able to work overnight shift as facility operates at night. Candidate must be flexible to work different shifts, schedules, holidays, days and overtime as needed.Responsibilities Manufactures radioactive isotopes (includes synthesis set up, hot cell manipulations, distribution) Conducts quality control testing of each batch (utilizing gas chromatograph, dose calibrator, multi-channel analyzer, TLC plate scanner, high pressure liquid chromatograph, analytical balance, PTS, laminar flow hood and fume hood) Performs environmental and personnel monitoring in ISO 5, ISO 7, and ISO 8 environments Works in ISO 7 cleanroom to make product vials and customer vials for use in drug production Coordinates daily production run schedule based on customer and pharmacy needs Demonstrates strong documentation practices, oral communication, and writing skills. Performs clerical and administrative tasks, including maintenance of daily production records, report preparation and maintenance records Manages SAP Inventory (includes receiving materials, properly inspecting materials for use, and maintaining proper cycle counts) Performs daily radiation safety tasks, along with general lab cleaning Ability to troubleshoot equipment issues Advanced chromatography skills Provide feedback on method development around time of Tech Transfer Communication with external innovator/sponsor* Ability to lead; judgement to prioritize quicklyQualifications Bachelor’s degree in related field, or equivalent work experience preferred. Sciences preferred 2 – 3 years HPLC experience preferred Lab experience highly preferred Must be able to work overnight shift (Facility operates at night.) Prior experience in manufacturing, preferably in a controlled environment and/or regulated industry preferred Effective written and verbal English communication skills required Able to repeatedly follow detailed processing instructions Ability to manage several tasks at the same time; Ability to evaluate operating conditions and exercise sound judgment and problem solving skills. Ability to manage weight up to 75 pounds Ability to see fine particulate and differentiate colors in liquid solutions. Ability to hear, write (English), and speak (English) clearly in order to communicate in manufacturing setting. Manual dexterity required for equipment operation and occasional reach and lifting of small objects.* Ability to be an effective team member.*What is expected of you and others at this level Applies basic concepts, principles and technical capabilities to perform routine tasks* Works on projects of limited scope and complexity* Follows established procedures to resolve readily identifiable technical problems* Works under direct supervision and receives detailed instructions* Develops competence by performing structured work assignmentsAnticipated hourly range: $30.10 per hour - $42.90 per hourBonus eligible: NoBenefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being.* Medical, dental and vision coverage* Paid time off plan* Health savings account (HSA)* 401k savings plan* Access to wages before pay day with myFlexPay* Flexible spending accounts (FSAs)* Short- and long-term disability coverage* Work-Life resources* Paid parental leave* Healthy lifestyle programsApplication window anticipated to close: 06/24/2026 *if interested in opportunity, please submit application as soon as possible.The hourly range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate’s geographical location, relevant education, experience and skills and an evaluation of internal pay equity.*Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply.Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.*To read and review this privacy notice clickHeadquartered in Dublin, Ohio, Cardinal Health, Inc. (NYSE: CAH) is a distributor of pharmaceuticals, a global manufacturer and distributor of medical and laboratory products, and a provider of performance and data solutions for healthcare facilities.We are a crucial link between the clinical and operational sides of healthcare, delivering end‐to‐end solutions and data‐driving insights that advance healthcare and improve lives every day. With deep partnerships, diverse perspectives and innovative digital solutions, we build connections across the continuum of care.With more than 50 years of experience, we seize the opportunity to address healthcare's most complicated challenges — now, and in the future. #J-18808-Ljbffr

In a world of vibrant color, INX stands out by blending art, science, and sustainability into every drop of ink we make. We’re globally recognized for our innovation, and we’re A Great Place to Work-Certified company! INX International is the third largest producer of inks in North America with full-service subsidiaries in Europe and South America. We offer a complete line of ink and coating solutions technology for commercial, packaging and digital applications. We expertly blend pioneering technology with a deep commitment to the environment. Dedicated to coloring a safe and sustainable future one print at a time, you can see our color chemistry on beverage cans, food and household packaging, clothing, banners, billboards and more. Investing in and protecting our employees is the key to our success. Our average employee has been with us 12 years, and we recognize the significant experience and the continuous dedication of our team members. We’re actively seeking new talent with new ideas as we continue to provide sustainable products, service and innovation to the printing and packaging markets. Join us in coloring a safe and sustainable future! Job Description We are seeking a motivated R&D Chemist to join our Edwardsville, KS laboratory team. This role is ideal for both experienced chemists and recent college graduates who are eager to build technical expertise and grow within a supportive, fast‑paced environment. Our Energy Cure Laboratory is backed by a strong technical foundation, with many team members bringing over 20 years of experience with INX International. INX is a leading provider of energy‑curing technologies for key markets such as low‑migration inks and coatings for packaging. As an R&D Chemist, you will contribute directly to the advancement of these technologies. We offer a collaborative culture, hands‑on training, and opportunities for autonomy. Team members also engage with customers and may travel occasionally to support internal and external partners. Primary Responsibilities Troubleshoot and support existing technologies, including assisting with customer‑driven challenges Develop new energy‑curing technologies based on customer and market needs Evaluate raw materials and optimize formulations for performance and cost efficiency Provide technical support to plant operations Prepare technical reports and documentation for customers and the sales team Maintain and ensure proper operation of laboratory equipment Qualifications Required Qualifications Bachelor’s degree in a STEM‑related discipline Strong math and science proficiency Accurate and organized recordkeeping skills Effective written, verbal, and reading‑comprehension skills Ability to interpret data and draw sound technical conclusions Color vision proficiency is essential for this role Preferred Qualifications Knowledge of energy‑curing printing processes (UV/LED flexographic, offset, or coatings) Five years of relevant industry experience Formulation experience in inks or coatings SAP experience Experience with analytical instrumentation such as GC/MS, FTIR Note for New Graduates: Candidates who recently completed their degree and demonstrate strong academic performance, laboratory skills, and a willingness to learn are encouraged to apply. We provide training, mentorship, and development opportunities to help new chemists succeed. Additional Information We offer a competitive salary with excellent benefits including medical, dental, vision, life insurance, disability, pet insurance, HSA and FSA, 401(k), and more. Through our programs, which now include Paid Volunteer Time Off and Paid Parental Leave , we support the needs of our employees, their dependents, and their communities by providing a benefit package that is easy to understand, easy to access, and affordable for all our employees. Don’t just choose a job; choose a career that emphasizes employee growth in a safe, environmentally conscious culture. Embark on your Colorful Career with us! We require post-offer, pre-employment drug screens, physicals, and background checks. Equal Opportunity Employer: disability/veteran. Job Location #J-18808-Ljbffr

United Cerebral Palsy of Georgia seeks an Analytical Chemist in Vernon Hills, IL for a 12-month contract. The candidate will provide analytical chemistry support for client products and participate in stability testing programs. A BS/MS in Chemistry/Pharmaceutics and 2-4 years in pharmaceutical analytical chemistry are required, along with hands-on experience in wet-chemistry and instrumental techniques like GC and HPLC. This position allows a chance to engage with various functional areas including Regulatory and Quality. #J-18808-Ljbffr

Chemist – Mapleton, IL Arxada is a global specialty chemicals business that’s committed to solving the world’s toughest preservation challenges through better science. With a proud history of innovation dating back more than a century, we aim to help our customers develop more sustainable solutions that protect and maintain the health and wellbeing of people and extend the life of vital infrastructure while working to reduce our and our customers’ ecological footprint. Sustainable preservation is one of our top priorities. We are making significant strategic investments that will not only decrease our own environmental footprint, but also help customers adapt to long‑term environmental and social change through the development of cleaner, greener solutions. Arxada is looking for a Chemist that performs tasks and testing in support of the manufacturing plant, wastewater operations, logistics, and quality department. Maintains and reviews laboratory records in compliance with ISO 9001 and EFfCI. This role is located in Mapleton, IL. The expected salary range for this union role is 37.44 an hour. Actual compensation may vary depending on experience, education, training, certification, location, and other job‑related, non‑discriminatory factors permitted by law. This role is also eligible to earn a short‑term incentive bonus and the following benefits: 401(k) plan, medical, dental, vision, life, and disability insurance, paid time off, paid holidays, and paid sick leave. Essential Job Functions Comply with all corporate and plant policies, procedures, guidelines, and work instructions pertaining to safety; and attend all mandatory safety meetings and training sessions (includes wearing proper PPE) Performs routine and non‑routine laboratory tests in an accurate and timely manner and records results of analyses in the appropriate logbooks and systems Ensure GDP is used within Quality meeting ALCOA standards, data accuracy, data integrity, legible, contemporaneous (recorded at time of event), original, and identifiable Conduct tasks in accordance with appropriate standard operating procedure, work instruction, etc. Fills in gaps in the shift and wastewater schedule as needed including 12 hour shifts, overnight, and weekend Product release including packaging, raw materials, finished products, and bulk shipments Perform calibrations and ISO 9001 checks (daily and monthly) Perform weekly ISO 9001 checks every Tuesday as needed Identifies areas of improvement within the Quality department Creates batch numbers in SAP for the release of products for packaging and bulk shipments Maintains laboratory equipment and consumables (i.e. gas cylinders) Perform data review and verification Utilize and maintain proper housekeeping in your work area Maintains and calibrates analytical instrumentation and reagents according to written procedures and schedules as needed Makes, backfills, and restocks reagents and standards as needed Supports waste water testing as neededPerform other duties as assigned Qualifications & Experience 3–5 years experience in a lab setting Bachelor’s degree in Chemistry or other science discipline Medical First Responder certification (or ability to obtain within 1 year) preferred Excellent written and verbal communication skills Reliable time‑management skills and the experience to organize and coordinate multiple projects at once Wet Chemistry, HPLC, GC, Auto‑titrator, COD experience preferred High proficiency in Microsoft Office and other office productivity tools, with quickness to learn new software and systems Arxada is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law. #J-18808-Ljbffr

Overview Stepan is seeking a Chemist to join our Polymers R&D team in Northfield, Illinois. This onsite laboratory-based role focuses primarily on rigid foam applications and offers the opportunity to support innovative product and formulation development for rigid spray foam and PIR insulation applications. The Chemist will be responsible for operating and maintaining polyurethane foam processing equipment, developing polyols and formulations, and conducting a variety of laboratory activities including foam formulation, application development at both small and large scale, physical property testing, fire testing, and analytical testing. Responsibilities Operate and maintain polyurethane foam processing equipment. Develop polyols and formulations for rigid foam applications. Conduct laboratory activities including foam formulation, application development at small and large scale, and physical property testing. Perform fire testing and analytical testing as part of product development and quality assurance. Qualifications 1-5 years working in a laboratory environment and practicing safe laboratory procedures. Ability to work collaboratively in a team environment. Good mechanical aptitude with machine operation and problem-solving experience. Some polymer and/or material science experience is desired. Demonstrated hands-on experience in analytical techniques such as titration, rheometry, TGA, or other wet chemical testing is desired. Strong attention to detail, with good organization and documentation skills. Strong communication skills in written, verbal and presentation formats. Proficiency in all Microsoft Office applications and willingness to learn specific database and web applications. Ability to work in the Northfield laboratory. Must be able to lift 50 pounds. Comfortable using a bandsaw. Education B.S. Degree in Chemistry or related field Pay Pay Range: $58,000 - $76,000. The salary range for this position is determined by considering a variety of factors such as skills, experience, qualifications, and the location of the position. Benefits Discretionary Bonus Medical, Dental, and Vision Insurance 401K with Match Profit Sharing Paid Time Off (PTO) Short-Term and Long-Term Disability (STD / LTD) Dependent Care Flexible Spending Account (FSA) Health Savings Account (HSA) Paid Parental Leave Adoption Assistance Reactions – Recognition Program Employee Assistance Program (EAP) EEO and Eligibility Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. Stepan Company does not accept or retain unsolicited resumes or phone calls and/or respond to them or to any third party representing job seekers. We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender, gender identity or expression, sexual orientation, national origin, genetic information, disability, age, veteran status, or any other status protected by applicable law. About Stepan Stepan Company is a global specialty and intermediate chemical manufacturer with a long-standing history and a broad portfolio across industries. We are committed to safety, sustainability, and a growth-oriented culture. We celebrate diversity and strive to create an inclusive environment for all employees. #J-18808-Ljbffr