Quality control analyst jobs in Illinois - 300 jobs

Pride Health is hiring a Quality Control Technician to support our client's medical facility based in Elmhurst, Illinois. This is a 13-week contract job opportunity and a great way to start working with a top-tier healthcare organization! Job Summary: The Sterile Processing Quality Control Technician ensures the highest standards of instrument cleanliness, assembly accuracy, and quality assurance in sterile processing operations. This role combines hands-on technical processing responsibilities with detailed inspection and documentation tasks critical to patient safety and process reliability. This position focuses on quality assurance beyond standard sterile processing technician duties, ensuring compliance with all regulatory and internal standards while maintaining an unwavering commitment to safety and process excellence. Job Responsibilities: -Follow all ANSI/AAMI standards, manufacturer Instructions for Use (IFUs), SOPs, and company Work Instructions. -Decontaminate used surgical instruments and equipment using proper PPE and protocols. -Disassemble, clean, and reassemble complex surgical instruments as required. -Accurately assemble and package instrument trays and sets per guidelines. -Operate washers, sterilizers, and other processing equipment safely and effectively. -Inspect instruments for cleanliness, functionality, and damage prior to packaging. -Document missing or damaged instruments per SOPs. Required Skills & Experience: -Hands-on experience in sterile processing, demonstrating proficiency in decontamination, assembly, and sterilization procedures. -Strong attention to detail. -Ability to work effectively under pressure in a fast-paced, team-oriented environment. -General knowledge of surgical instruments and processing protocols. -Knowledge of sterilization techniques, including steam sterilization and infection control practices. -Familiarity with ANSI/AAMI standards and manufacturer Instructions for Use (IFUs). Additional Information: Location: Elmhurst, Illinois Schedule: 2nd Shift- 3 pm-11:30 pm Pay Range: $24/Hr. - $28/Hr. Start: 01/26/2025 *Offered pay rate will be based on education, experience, and healthcare credentials. Interested? Apply now! About Pride Health As a certified minority-owned business, Pride Global and its affiliates - including Russell Tobin, Pride Health, and Pride Now - are committed to creating a diverse environment and are proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, pregnancy, disability, age, veteran status, or other characteristics. Pride Global offers eligible employee's comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance, and hospital indemnity), 401(k)-retirement savings, life & disability insurance, an employee assistance program, legal support, auto, home insurance, pet insurance, and employee discounts with preferred vendors.

This full-time day shift position reports directly to the Quality Manager. Please read the information in this job post thoroughly to understand exactly what is expected of potential candidates. This position is responsible for in-process and final visual/dimensional inspection functions of steel fabrications, piping, pressure vessels, and finished machined parts. Working conditions are mainly in a shop environment, with a small percentage of time spent in an office environment. Exposure to possible shop hazards including but not limited to welding fumes, heat, flash burns, skin burns, high noise level and eye injuries from welding arc and grinders, as well as industrial machinery, and fork truck traffic. Physical requirements include periods of standing, walking, climbing, and bending, with minimal heavy lifting. xevrcyc Working at heights or in tight spaces may be required at times.

This position is responsible for maintaining quality control processes, testing products, and recording and analyzing results gathered to ensure Sherwin products meet quality specifications. This position is responsible for testing production batches according to specific written testing methods and identifying issues of both in-spec and out-of-spec data. The technician will interpret results and historical data to ensure the product meets or exceeds the customer requirements for quality, as well as provide instructions to production personnel regarding adjustments to batches as needed. Additional Information: Shift: Monday - Thursday 10:00am - 8:30pm This position is also eligible for bonus based on performance and subject to the terms of the Company's applicable plans. This position is eligible for sick leave benefits, funeral leave, idle holiday pay, and, provided eligibility requirements in the Collective Bargaining Agreement are satisfied, paid temporary employee flex days Job duties include contact with other employees, operating heavy machinery, and access to proprietary information, raw materials, finished merchandise, and/or other items of value, and such access may be supervised or unsupervised. The Company therefore has determined that a review of criminal history is necessary to protect the business and its operations and reputation and is necessary to protect the safety of the Company's staff, employees, and vendors Responsibilities Ensure all tests are completed and results meet all specifications before going to the next production process Enter all batch data into the electronic batch records system Generate appropriate paperwork as needed per customer specifications Gather and send customer samples as required Utilize appropriate computer systems to ensure effective testing of products Determine disposition of non-compliant finished goods Place non-conforming material on hold as needed Support the ISO Management Systems and Safety Systems. Maintain inventory of lab supplies Identify and communicate product issues to other departments as needed Create, maintain, and update standard operating procedures for Quality Department to meet ISO requirements Assist in training of other lab technicians as needed Qualifications Minimum Requirements Must be at least eighteen (18) years of age Must be legally authorized to work in the country of employment without needing sponsorship for employment work visa status now or in the future Preferred Qualifications Have at least one (1) year of experience working in a quality control laboratory Have at least one (1) year of experience working in a manufacturing or distribution facility Have an Associate Degree or higher in Chemistry About Us At Sherwin-Williams, our purpose is to inspire and improve the world by coloring and protecting what matters. Our paints, coatings and innovative solutions make the places and spaces in our world brighter and stronger. Your skills, talent and passion make it possible to live this purpose, and for customers and our business to achieve great results. Sherwin-Williams is a place that takes its stability, growth and momentum and translates it to possibility for our people. Our people are behind the strength of our success, and we invest and support you in: Life ... with rewards, benefits and the flexibility to enhance your health and well-being Career ... with opportunities to learn, develop new skills and grow your contribution Connection ... with an inclusive team and commitment to our own and broader communities It's all here for you... let's Create Your Possible At Sherwin-Williams, part of our mission is to help our employees and their families live healthier, save smarter and feel better. This starts with a wide range of world-class benefits designed for you. From retirement to health care, from total well-being to your daily commute-it matters to us. A general description of benefits offered can be found at Click on "Candidates" to view benefit offerings that you may be eligible for if you are hired as a Sherwin-Williams employee. Compensation decisions are dependent on the facts and circumstances of each case and will impact where actual compensation may fall within the stated wage range. The wage range listed for this role takes into account the wide range of factors considered in making compensation decisions including skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. The wage range, other compensation, and benefits information listed is accurate as of the date of this posting. The Company reserves the right to modify this information at any time, with or without notice, subject to applicable law. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable federal, state, and local laws including with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act where applicable. Sherwin-Williams is proud to be an Equal Employment Opportunity employer. All qualified candidates will receive consideration for employment and will not be discriminated against based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, age, pregnancy, genetic information, creed, marital status or any other consideration prohibited by law or by contract. As a VEVRAA Federal Contractor, Sherwin-Williams requests state and local employment services delivery systems to provide priority referral of Protected Veterans. Please be aware, Sherwin-Williams recruiting team members will never request a candidate to provide a payment, ask for financial information, or sensitive personal information like national identification numbers, date of birth, or bank account numbers during the application process.

Dexter Magnetic Technologies supplies specialized magnetic solutions and components to demanding applications in the medical, aerospace, defense, semiconductor manufacturing, oil and gas, and industrial end markets. Dexter's engineers solve complex customer problems with innovative solutions, winning business based on quality, customer support, and application engineering expertise. For more information on Dexter Magnetic Technologies, please visit: Basic Purpose and Objective of the Position The QC Inspector 1 is responsible for ensuring raw materials, components, sub-assemblies, and finished products meet the required quality standards and specifications as defined by the Quality Management System (QMS). This position plays a critical role in upholding Dexter's commitment to delivering high-quality products by conducting thorough inspections and collaborating to address quality concerns. Major Responsibilities - Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions: An employee in this position will perform tasks directly related to: Inspecting incoming materials, components, and assemblies to verify compliance with specifications, customer requirements, and engineering standards. Managing non-conforming materials by tagging, documenting, and placing items in quarantine while coordinating with relevant teams for resolution. Recording inspection results accurately in the company's systems in adherence to established work instructions. Preparing initial packaging, generating bar code labels, and completing required documentation to ensure traceability. Actively participating in the resolution of quality concerns by collaborating with cross-functional teams to make timely decisions on raw materials and components. Maintaining a clean, safe, and organized work environment while practicing 5S methodologies. Supporting other QC Inspectors with basic inspection tasks as needed and assigned. Performing additional duties as assigned to support quality initiatives Hourly Rate $22 - $23 per hour Education and Experience: High school diploma or equivalent is required; post-secondary education is preferred. Minimum of 3 years of experience in a manufacturing or quality control environment. Successful Essential Skills: Strong understanding of mechanical drawings and blueprints. Proficiency in using inspection tools such as calipers, micrometers, and gauges. Strong computing skills, including experience with MS Office and MRP systems (preferably Epicor). Excellent time management and organizational abilities. Ability to communicate effectively across different organizational levels, promoting collaboration and resolution of non-conformance issues. We offer a comprehensive benefits package, including Medical/Rx, Dental, Vision, Flexible Spending Accounts, Basic Life/AD&D (includes coverage for dependents 100% Company paid), Short-Term Disability, Long-Term Disability (100% Company paid), Supplemental Life/AD&D, 401(k) with Company match, tuition assistance after 1 year, paid time off, and 11 paid holidays. Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

Quality Control / Non Destructive Testing / NDT / NDE / QC We offer you: CAREER GROWTH SUPERIOR BENEFITS COMPANY WIDE BONUS PLANAWESOME BENEFITS ESOP - EMPLOYEE STOCK OWNERSHIP PLAN HOURS: 4 pm - 4 am - 2nd Shift OR a similar 12 hour shift 10% shift premium Looking for detailed oriented and analytical manufacturing individuals who want a long-term career. We have locations in Spring Grove, IL, Clinton, WI and Franklin Park, IL. We conduct a hair follicle pre-employment drug screen. Scot Forge is a 130 year-old, 100% employee-owned company that manufactures custom open die and rolled ring forgings for demanding applications all over the world. ESSENTIAL FUNCTIONS: Inspection of incoming materials, process and final product inspection, evaluation of product conformance, data review and analysis and NDE inspection reports. Set up, calibrate and operate various non-destructive testing instruments to verify steel integrity. Calibrate and perform NDE in accordance with NADCAP standards. Obtain and maintain internal certifications in NDE disciplines - Ultrasound (UT), Penetrant Testing (PT) and Magnetic Particle Testing (MT) as part of NDT role. Obtain Niton, Brinell, and Final Inspection certifications. Review shop order, specifications, and production prints to determine appropriate testing and inspection parameters. Prepare print of non-conforming material indicating a description and location of non-conformance. Prepare documentation to be used to submit deviation and non-conformance reports for material out of specification. Prepare any required inspection records/documentation including dimensional reports and customer provided documentation of inspection. Participate in required equipment training for safe use of Crane, Chain and Rigging, Fork trucks, use of etchants, and the use of special evaluation tools such as the Niton gun and radiation detectors. Participate in required documented procedure training as required by position and or assignment of supervisor. Communicate with Sales, Process Engineering, Metallurgy Lab and Production departments as required to confirm product specifications or to inform of product or process non-conformance. Inspect and evaluate products on customer premises or at Scot Forge for customers or customer's representatives. Asks questions if a process is unclear, or there's safety, or quality concerns. Understand and follow the Scot Forge safety and quality policies. QUALIFICATIONS: Required: High School Diploma or Equivalent 1 or more years of manufacturing/ heavy equipment / Quality Control, Quality Assurance experience Micrometer, caliper and gauge experience Preferred: Associated Degree (AAS or equivalent) - Preferred Certifications ASNT ACCP (UT, PT, MT level 2); ASQ CQI or CQT Minimum 1 to 3 years applied training in NDE Level 1or Level 2 NDT certification Metal fabrication experience High level QA or QC reporting experience Forklift experience - sit down Manufacturing or Production experience Ultrasound / Ultrasonic testing experience BENEFITS: A few of our amazing benefits include... Employee Stock Ownership Plan Profit Sharing Bonus Medical Dental Life Insurance Vision Company provided Life Insurance Prescription Drug Plan 401K and Roth Plan Paid vacation and holidays. Short term disability Long term disability Tuition Reimbursement Scot Forge is a 130 year-old, 100% employee-owned company that manufactures custom open die and rolled ring forgings. At Scot Forge, we help our customers with forged solutions from the world's physical infrastructure, energy, and transportation to manufacturing, mining, and our national defense. From the wheels of NASA's Curiosity Mars Rover to mission critical components for nuclear submarines, to large hydraulic cylinders for the largest mining trucks on the planet, Scot Forge creates the precision forged metal parts used in demanding applications all over the world. #1813 We are proud to be an Equal Employment Opportunity employer: M/F/Disabled/Vets encouraged to apply. We maintain a drug-free workplace and perform pre-employment hair follicle substance abuse testing

Our client is a provider of flavorings and ingredient solutions to the food, beverage, and nutraceutical industries. This position is responsible for formulating, testing, and evaluating flavor compounds and blends to meet the diverse needs of our clients and products. You will collaborate closely with cross-functional teams, including product development, quality assurance, and regulatory compliance, to ensure that all flavor formulations align with industry standards and consumer preferences. Job Responsibilities: Create and formulate new flavor profiles for a variety of food and beverage products, ensuring they meet customer specifications and market trends. Conduct sensory testing and analysis of flavors to evaluate their performance in different applications, using both quantitative and qualitative methods. Work directly with customers to finalize customer projects as is required Maintain accurate records of formulations, experimental data, and sensory evaluations, and prepare comprehensive reports summarizing findings and recommendations. Work closely with cross-functional teams, including product development, marketing, and production, to support the successful launch and optimization of new flavors. Provide technical support and training to internal teams and clients on flavor properties, applications, and trends. Collaborate with ingredient suppliers and vendors to source high-quality raw materials and explore new flavor ingredients. Ensure that all flavor formulations adhere to safety standards and regulatory compliance, including labeling and allergen management. Aid in training Flavor Apprentice(s) in preparation for testing with the Society of Flavor Chemists The Ideal Candidate Will Have: Degree in food science, physical sciences, or related field required Desired 7+ years of flavor development experience and a certified member of the Society of Flavor Chemists Experience with the creation and scaling of reaction flavors Preferred experience in Flavor formula entry in Sage X3, E-Book File, and Product Vision is highly desirable What we will offer: An attractive salary, and benefit package An amazing opportunity to grow your career with an industry leader If you are someone that is ideal for this position, please submit your resume in Microsoft Word format. We look forward to hearing from you.

Technetics Group is a leading designer and manufacturer of custom engineered mechanical seals for rotating shafts and precision components for aerospace and specialized industrial applications. Technetics Group is a division of is one of eight operating divisions of Enpro Industries, Inc. #Technetics Group JOB SUMMARY: The Quality Technician I is responsible for the metrology of product manufacturing and ensures the dimensions and form of the product meets Purchase Order and Drawing requirements. This position is an entry-level Inspector role within a manufacturing environment. The primary focus is on learning and performing basic inspection tasks to ensure product quality, while gaining exposure to CNC machining processes. Candidates will receive training and guidance to develop skills in dimensional inspection, use of measurement tools, and adherence to quality standards. Essential Functions: Safety: Embrace the values of the Enpro safety pledge in each of the responsibilities below. Participate in the organization's safety culture and aim to continuously improve safety within all aspects of your work. Respect: Foster a work environment that promotes mutual respect of all colleagues and creates an environment focused on a dual-bottom line. Excellence: Promote the Sealing Technologies and Enpro culture around creating value and driving excellence in our organization by: Supports production by performing basic quality inspections to ensure products meet established standards Contributes to maintaining product quality and consistency Low to moderate complexity; handles routine inspection tasks using standard procedures Makes decisions within defined parameters for basic quality assessments Refers complex issues to higher-level technicians or Quality Engineers Maintains clear and accurate inspection records Perform basic inspections of products and materials to ensure compliance with specifications Use measuring tools to assess product dimensions and quality Document inspection results and report discrepancies Assist in maintaining inspection equipment and work area cleanliness Maintains a clean and organized work area, adhering to 5S standards Job Competencies & Qualifications: Communicates effectively with colleagues and supervisors Familiarity with basic measuring instruments (e.g., calipers, micrometers) Ability to read and interpret simple blueprints and specifications Basic computer skills for data entry and documentation Requirements: Education: HSD / GED Experience: 0-2 Years of experience in a manufacturing or quality control environment SUPERVISORY RESPONSIBILITIES This position has no direct supervisory responsibilities. ADDITIONAL RESPONSIBILITIES: Performs other duties as assigned by supervisor. PHYSICAL REQUIREMENTS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to stand. The employee frequently is required to walk; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. The employee is occasionally required to sit. The employee must regularly lift and/or move up to 15 pounds, frequently lift and/or move up to 35. Specific vision abilities required by this job include close vision, color vision, peripheral vision, depth perception, and ability to adjust focus. Technetics is a subsidiary of Enpro, a leading industrial technology company focused on critical applications across many end-markets, including semiconductor, industrial process, commercial vehicle, sustainable power generation, aerospace, food and pharma, photonics and life sciences. At Enpro, we believe that diversity drives innovation and inclusion fosters growth. We are committed to creating a workplace where everyone feels valued and respected. Our employment decisions are based on merit, qualifications, and business needs, without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability, genetic information, marital status, military service, or any other status protected by applicable law. If you require accommodation due to a disability at any time during the recruitment and/or assessment process, please contact Human Resources, and we will make all reasonable efforts to accommodate your request. Enpro Inc. is an equal opportunity employer. Legal authorization to work in the United States is required. We will not sponsor employment visas now or in the future for this job. This position involves access to information that is subject to U.S. export controls. Any job offer made will be contingent upon the applicant's capacity to serve in compliance with U.S. export controls. Enpro carefully considers a wide range of compensation factors including thebackground, education, training,and experience required, as well as geographicconsiderations such as cost of labor, and applicable local andstate laws. These considerations can cause offered compensation to vary. The hiring range for this position istypically $21.85/hr - $32.78/. The actual offer will be based on the individual candidate.Bonus,gainshare, and/or equitymay be eligible for this position.Enpro offers a range of benefits including, butnotlimited to medical, dental, vision, life, 401(k) matching, and other supplementalinsurance options.

The NUFSM Department of Physical Medicine and Rehabilitation, in collaboration Shirley Ryan AbilityLab, seeks a full-time non-tenure-eligible Team Scientist at the rank of Assistant Professor, Associate Professor, or Professor. The position is based at Shirley Ryan AbilityLab, with opportunities for collaboration with Northwestern University Departments of Biomedical Engineering, Mechanical Engineering, Physical Therapy & Human Movement Sciences, Neurology, Neurosurgery, Neuroscience, and Physical Medicine & Rehabilitation. Responsibilities include: * Develops and submits research proposals and grant applications to secure external research funding from agencies such as the NIH, VA, NIDILRR, DoD, NSF and private foundations * Ensures that scientific and regulatory milestones of specific projects are met * Publishes original studies in refereed journals that advance our understanding of motor control, and translation science linked to neurologic illness. * Demonstrates leadership activity in professional organizations such as the Society for Neuroscience, the International Society for Society for Neuroscience, Neural Control of Movement, Progress in Motor Control, etc. * Contributes to the educational of highly qualified personnel including graduate students, post-doctoral fellows, medical students, and residents. * Participate in and collaborate on Department activities, as requested by the Department Chair. Qualified candidates: * Knowledge of measurement and statistics principles acquired through a Ph.D. in a scientific discipline from an accredited school and successful completion of a postdoctoral fellowship. * Minimum 2 years of related experience with an expert knowledge of scientific principles and concepts. Reputation as emerging leader in field with sustained performance and accomplishment. * Uses professional concepts in accordance with institute objectives to solve complex problems in creative and effective ways. * Demonstrated success in technical proficiency, scientific creativity, collaboration with others and independent thought. * Works on complex problems and designs/conducts research projects in which analysis of situations or data requires an in-depth evaluation of various factors. * Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results. * Requires proficiency in writing to prepare grant proposals, research reports and other publications, and explain complex results to a lay audienc * Interpersonal skills needed to communicate effectively with other staff members, fellow researchers * May determine methods and procedures on new assignments and may provide guidance to other lower-level personnel. * Commitment to teaching and teaching ability are requirements The start date is negotiable and the position will remain open until filled. When applying, please upload a CV and cover letter describing your interest and alignment with the position. Also upload this completed list of references form to suggest the names of individuals who could write letters of reference on your behalf. Please read ALL instructions and make preparations before proceeding to the application page: * Applications will only be accepted via online submission (see link below). * Please prepare all documents in advance as Adobe PDF files, and please be sure all information is entered correctly and accurately (especially names and email addresses), as there will be no opportunity for online revision after your application has been submitted. * All required fields in the application form are marked with an asterisk and must be filled before clicking the "Submit" button. * Be aware that incomplete applications cannot be saved. Applications accepted here: Apply for Job Northwestern University is an Equal Opportunity Employer and does not discriminate on the basis of protected characteristics, including disability and veteran status. View Northwestern's non-discrimination statement. Job applicants who wish to request an accommodation in the application or hiring process should contact the Office of Civil Rights and Title IX Compliance. View additional information on the accommodations process.

Overview Salary: $51,000 - $64,000 Annually Summary: The Quality Control Technician will implement and comply with quality assurance methods and procedures to ensure products and materials are produced in accordance with specifications in a safe and efficient manner. Principal Duties and Responsibilities: Quality Control Analysis: •Conduct tests and inspect concrete to evaluate quality or conformance to specifications •Sample and evaluate quality of materials related to concrete •Monitor equipment operation to ensure that concrete is within tolerance •Record inspection or test data, such as slump, air content, unit weight, temperature, or moisture content •Input test data into company quality control software •Test hardened concrete for compressive strength •Input strength results into company quality control software •Analyze, evaluate, and resolve customer concerns involving specific conditions, situations, quantities, and other influences associated with product •Manage and maintain quality control software for assigned area Production and processing: •Perform aggregates and batch plants tests including aggregate gradation and moisture tests for State and spec projects as required Communication Skills: •Provide information to supervisors, co-workers, and contractors via phone, e-mail or in person •Effectively communicate with dispatch office to successfully ship and test concrete Global Responsibilities: •Regular attendance and physical presence at work is an essential function of this position •This job may require additional duties not listed above and the employee may be asked to perform those duties to meet business needs Qualifications: Education/Specialized Knowledge/Professional Certifications: •High School Diploma or equivalent required •Bachelor's degree in related field preferred •ACI Level 1, NICET Certified or NRMCA Short Course completion on aggregates or concrete are required •Valid driver's license required •IDOT PCC Level I or WDOT PCCTEC I certification(s) or higher are preferred(IL South, IL North, and WI region only) •Knowledge of raw materials, production processes and quality control are preferred Experience: •Experience in related field preferred Skills/Abilities: •Able to read, write, and speak English preferred •Able to operate a smart phone/device •Proficient in Microsoft Office Suite Working Conditions: •Operation within a fast-paced environment •Exposed to moving mechanical parts, vehicles, heavy construction equipment, toxic or caustic chemicals, and outside weather conditions •Noise level is usually moderate, but can be high and requires personal hearing protection on occasion at job sites, plants and laboratories •Must be able to work through stressful situations while maintaining professionalism and composure •Local travel required Physical Requirements: •Regularly required to talk or hear; frequently is required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms •Occasionally required to sit; climb or balance; and stoop, kneel, crouch or crawl •Must be able to stand and move about job sites with uneven and unpaved ground while managing concrete delivery onsite •Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus •Must be able to frequently bend in order to obtain samples from stockpiles or ground, climb ladders with buckets of admixtures, and push wheelbarrows of concrete •Must be able to operate buttons, levers, and other controls located on various equipment •Must be able to work long and flexible hours as necessary •Must be able to maneuver in and around our plants, yards and jobsites as necessary •Lift/Carry up to 55pounds frequently •Lift up to 100 pounds occasionally Benefits Information: At Ozinga, we care about the well-being of our team members both in and out of the workplace. That's why we're proud to offer a comprehensive benefits package designed to support your health, financial security, and overall quality of life. Our benefits include: • Medical, Dental, and Vision Insurance - Protecting your health and providing peace of mind. • Retirement Plan Options - Helping you build a secure future. • Voluntary Benefits - Helping you to cover unexpected expenses. • Work-Life Balance - Supporting flexibility so you can thrive in every area of your life. • Employee Assistance Program - Offering confidential support for personal and professional challenges. • Wellness Program - Promoting a healthy lifestyle through resources and incentives. We believe that when our co-workers feel their best, they can do their best. Join us and experience the difference of working for a company that values you! Ozinga is an Equal Opportunity Employer. We consider applications for all positions without regard to race, color, religion, creed, gender, national origin, age, disability, sexual orientation, citizenship status, genetic information, or any other legally protected status.

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: At MilliporeSigma, the Quality Control Scientist is responsible for performing multi-discipline analytical test methods for a variety of product lines to help achieve overall business objectives. This role is also responsible for maintaining the Product Stability, Product Retention, and Reverse Osmosis Water Quality Programs in accordance with the current regulatory guidelines. Additionally, this role supports Special Projects and Process Engineering analytical requirements to maintain existing, and future, business development. * Understands and works within a broad range of guidelines, standard operating procedures and/ or technical methods that involve a variety of routine work procedures with a moderate degree of supervision * Performs analytical testing on raw materials, intermediate products, and finished goods adhering to GLPs, GMPs, and EHS requirements * Performs laboratory activities in a timely manner to meet manufacturing and product delivery deadlines * Interprets analytical data relative to specifications, process controls, and other analytical references * Performs investigations on aberrant data and initiate out of specification reports * Maintains and control quality records in compliance with regulatory requirements * Conducts laboratory support functions. Maintains supply levels to ensure availability * Performs simple laboratory instrument upkeep including the cleaning, calibration, and the preventive maintenance of the instrument * Performs high-level instrument troubleshooting activities * Participates in audit readiness * May work a 2 week 12-hour shift cycle on either a day or night shift assignment Who You Are: Minimum Qualifications: * Bachelor's Degree in Biology, Chemistry, Microbiology, or other life science discipline OR * Associate's Degree in Biology, Chemistry, Microbiology, or other life science discipline AND 2+ years' work experience in a research or lab environment Preferred Qualifications * Knowledge of analytical chemistry, analytical microbiology, analytical biology, environmental monitoring, and plant hygiene processes and procedures * 1+ years of experience working in a cGMP Quality Control Laboratory * 1 + years of experience working with laboratory equipment such as (HPLC, GC, UV/Vis, TOC, AA, and KF) Pay Range for this position - $26-$44/hour The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

This position is responsible for providing analytical support and leadership within the quality organization to Operations at the Montgomery, Illinois facility. Key Responsibilities: Performs sampling, testing, and data reporting to ensure finished products, intermediates, and raw materials conform to release specifications. Provides analytical support to experimental orders. Follows all laboratory safety policies including safe handling of reagents and follows all chemical waste handling instructions according to VVF policies and procedures. Follows written lab procedures, or published standard methods or methods from compendia sources. Collects and analyzes data. Applies appropriate methodologies, data interpretation techniques, statistics, and computer software to assist in resolving production difficulties. Performs scheduled instrument checks and calibrations; assists in preparing, standardizing and labeling standard solutions. Complies with regulatory and GMP requirements relevant to job responsibilities in a GMP laboratory. Maintains accurate laboratory notebooks and other laboratory records. Troubleshoots the performance or accuracy issues of basic laboratory analytical instruments (including HPLC, Karl Fischer, and autotitrator instrumentation). Utilizes software programs for data collection and release documentation (ie: LIMs, LabX, Microsoft Dynamics GP, Excel, Office, etc) Initiates nonconforming reports for packaging, raw materials, in-process and finished product as necessary. Authors SOP's and Work instructions as assigned to support the quality systems. Assists in training activities, as needed. Ensures compliance with Company and Government regulations. Qualifications Basic Minimum Requirements: Meet the legal minimum age requirement. Authorized to work in the United States. Bachelor of Science Degree in Chemistry or related field or equivalent combination of experience and education. Ability to work all shifts. Ability to work overtime as needed. Other Required Skills: Ability to work independently and as part of a team. Strong attention to detail, planning and organizational skills. Strong written, verbal and interpersonal skills. Preferred Qualifications: 2 plus years laboratory experience. Experience in the operation of analytical instrumentation and other lab equipment relevant to the job responsibilities. Proficient in lab instrument maintenance and troubleshooting with specific certification. Physical Requirements Able to sit for long periods of time utilizing a computer. Able to stand for long periods of time. Lifting up to 25 lbs. VVF is an equal opportunity employer. We evaluate qualified applicants, without regard to race, color, religion, national origin, sex or gender, age, disability, veteran status, sexual orientation, gender identity or expression, genetic information, including the perception that a person has any of those characteristics or that the person is associated with a person who has, or is perceived to have, any of those characteristics, or any other consideration made unlawful by applicable law. VVF is committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation because of a disability for any part of the employment process, please call Human Resources at ************** and let us know the nature of your request and your contact information.

Hentzen is a unique company in today's world. Since our founding in 1923, we've remained an independent, privately held organization committed to being a leader in the development and manufacturing of high-performance coatings. Our success is built on a foundation of innovation, dedication, and service-to both our customers and our employees. With over 100 years of experience, Hentzen has earned recognition as a technology leader and trusted partner in the aerospace, defense, and industrial markets. Our ability to custom-engineer advanced coatings tailored to meet the specific and challenging requirements of our customers sets us apart. This innovation comes to life in our state-of-the-art facilities, where our talented employees are empowered to solve complex problems through creativity and collaboration. If you're looking to join a company known for its technical excellence, employee commitment, and customer focus, Hentzen offers a rewarding and challenging opportunity to learn, grow, and make a meaningful impact. DEVELOPMENT CHEMIST - LIQUID R&D 1st Shift M-F Batavia, IL Plant The Development Chemist - Liquid R&D is responsible for the formulation, research, and development of new products and colors as well as improvement of existing products. The successful candidates will have an acceptable score on the color matching and math tests. DESCRIPTION OF ESSENTIAL DUTIES: Develop new products for customers per their requirements. Develop products and solve technical issues with a relatively minor amount of direction. Exercise wide discretion when solving challenges. Provide technical assistance for existing accounts. Build knowledge of analytical methods for solving problems. Train production and quality control personnel. Work with production personnel to solve problems. Exhibit demonstrated decision-making abilities. Plan activities for support personnel. Reduce or rework distressed products on hand to reduce inventory. Ability to travel up to 10% of time. As part of the housekeeping procedures, the employee may be involved with the disposal of hazardous waste. The initial training of how to properly dispose of hazardous waste will be performed by the Environmental and Safety department or the department supervisor. Annual training of the same will be performed by the EHS department. Perform other miscellaneous duties as assigned. QUALIFICATION REQUIREMENTS: Education level strongly preferred: Bachelor's degree in chemistry or related field. Experience level preferred: One to three years in a manufacturing or industrial setting, preferably in coatings or chemical environment. Ability to receive and provide instructions in a positive manner. Ability to read, understand and apply complex mathematical calculations. Exemplify core values, i.e., Integrity, Loyalty, Passion, Commitment, and Respect. Must be a high energy, results driven individual with excellent communication, computer, and decision-making skills. Ability to work independently, in a fast-paced team environment, with the proactive problem-solving skills and work ethic necessary for timely completion of projects. Excellent computer skills (Microsoft Office - Word, Excel, Outlook), ERP system and other office machinery. WORK ENVIRONMENT: While performing the duties of this job, the employee is frequently required to talk and/or hear, stand, and/or walk, use hands to finger, handle or touch objects or controls, and move from place to place. The employee is regularly required to sit, balance, stoop, and occasionally reach above shoulders. The employee occasionally must use foot/feet to operate machinery, climb, or balance and reach above the shoulders. The employee may regularly lift and/or move up to 65 lbs. Personal Protection Equipment is required during various processes in the production facility. Safety shoes, glasses, respirators, fire retardant uniform, and earplugs may be required when performing certain functions. Please send your resume to: Hentzen Coatings, Inc. Attn: Human Resources 6937 W. Mill Road Milwaukee, WI 53218 or APPLY ONLINE AT: Hentzen Career Center Hentzen Coatings, Inc. is an Equal Opportunity Employer, including Veterans and Individuals with Disabilities. *************** All candidates are subject to post-offer testing: including a job-related pre-employment physical, drug screen, and background check.

Animal Health Corporation Phibro Animal Health Corporation is a publicly traded, global organization with a rich history in animal health and nutrition as a manufacturer and marketer of medicated feed additives, vaccines, nutritional specialty products, and mineral nutrition. We strive to be a trusted partner with livestock producers, farmers, veterinarians, and consumers who raise or care for farm and companion animals by providing solutions to help them maintain and enhance the health of their animals. Phibro is a diversified company in manufacturing and marketing products for ethanol performance, microbials for plants, home and industrial applications, and specialty chemicals for various industrial markets. In addition to, Phibro's revenues are in excess of $1 billion and are supported by over 2,400 employees worldwide. At Phibro, people are our greatest asset. We strive to develop a diverse workforce that fosters an environment where people feel supported in openly sharing their creativity and skills that allows them to be the most successful that they can be. If you are interested in working for Phibro and feel that you do not meet all qualifications, we encourage you to apply as you might be the right candidate for this role or other positions. The Laboratory Analyst III is an integral part of our Quality team based out of our US - Chicago Heights, IL site. Hourly rate range for this position is $25.00 - $30.00 Position Details The Laboratory Analyst position supports the Medicated Feed Additives (MFA) business of Phibro in Chicago Heights, IL. The Quality Control laboratory provides testing and release support for multiple sites in the MFA network, in addition to analytical support for contract manufacturing. The preferred candidate will meet the criteria for an Analyst III, IV, or V level, as described below. Key Responsibilities Receives and prepares samples for analytical testing and initiation of stability studies. Performs physical testing of routine and non-routine samples with little supervision including but not limited to raw materials, in process testing, API & finished good release and stability testing. Supports the site quality, safety and production needs and goals compliantly. Works within cross-functional teams. Coordinates own work assisting the lab to complete priority projects. Completes all activities following site cGMP, Safety requirements and Phibro Standards. Conducts laboratory activities related to experiments, studies, and projects in support of production, laboratory, or other Phibro groups: Understands and follows GMP/GLP regulations. Data maintenance and record keeping are in accord with GMP and SOPs Participates in projects and follows through to completion. Supports laboratory operations using technical ability to run routine samples independently. Recognizes abnormal results and/or instrument problems and reports them to supervision providing input to cause and possible solutions. Key Responsibilities Continued Performs routine tests and experiments following compendial or standard procedures Has an understanding and has applied skills related to Lean & 5-S. Sets up, adjusts and operates laboratory basic equipment such as balances, pH meter, sieves, ovens and has an understanding and has used advanced laboratory equipment such as Viscosity, Karl Fischer, UV/VIS, HPLC, GC. Maintains and follows Standard Operating Procedures dealing with their work area and can apply knowledge to assist in other work areas. Generation of protocols and execution of projects with little oversight. May lead a project and be responsible for completion. May assist with the writing and revising of procedures. May be assigned to projects dealing with special samples needing method modifications, with close supervision. Records tests results on standardized forms and prepares reports describing procedures used. Prepares charts and graphs to assist in evaluation and interpretation of data. Key Responsibilities Continued Completes investigations into aberrant data and generation of summary reports for their own work, can apply problem solving techniques in a team environment. Considered a Subject Matter Expert in Procedures for their area, providing training in and out of their department. Maintains a safe and clean working area and assists others in same. Will work with Analysts, Scientists and Management staff on a routine basis for the receipt and preparation of QC Test Samples and Stability study samples. Follows good documentation practices. Adheres and demonstrates exemplary behaviors. Identifying EHS hazards and propose solutions to improve lab/safety compliance. Key Competencies AccountableAccepting DirectionAttendance and PunctualityAttentive ListeningCollaborativeCommunicating EffectivelyCritical ThinkingDelivering High Quality WorkDemonstrating InitiativeDetailed OrientedDisplaying Technical ExpertiseFollowing Policies and ProceduresInteracting with People at Different LevelsManaging TimePrioritizing and Organizing WorkProblem SolvingWorking SafelyTechnical Skills Requirements Excellent attention to detail. Ability to use and perform HPLC, UV, GC and other instrumental techniques. Ability to generate protocols and summarize data. Ability to communicate within and outside immediate department. May contact vendors and/or external customers for administrative and technical information. Ability to work weekends and off shifts, as needed. Computer literate with the following applications: MS Excel, Word, Access Ability to utilize application software such as: Empower, Trackwise, JDE. Familiarity with Lean concepts and 5-S. Skills High degree of time management skills and ability to handle multiple priorities and projects at once.Prioritizes and plans work activities, uses time efficiently and develops realistic action plans.Excellent Written and Verbal Communication SkillsProven ability to work effectively in a team environment.Education & Experience ANALYST III High School degree or equivalent with approximately 10 years lab experience, preferably in an FDA regulated environment; or 2-year degree with approximately 3 years' experience or B.S. degree in a related scientific field with approximately 1.5 years of experience. ANALYST IV High School degree or equivalent with approximately 15 years lab experience, preferably in an FDA regulated environment; or 2-year degree with approximately 5 years' experience or B.S. degree in a related scientific field with approximately 3 years of experience. ANALYST V High School degree or equivalent with approximately 20 years lab experience, preferably in an FDA regulated environment; or 2-year degree with approximately 10 years' experience or B.S. degree in a related scientific field with approximately 5 years of experience. Physical Requirements Operations of laboratory equipment Required to bend frequently Required to sit frequently Required to stand frequently Required to talk or hear constantly Required to use hands constantly Required to walk frequently Specific vision abilities include ability to adjust focus Specific vision abilities include close vision Specific vision abilities include depth perception Specific vision abilities include distance vision Specific vision abilities include perpheral vision To learn more about Phibro Animal Health's competitive benefits package, please click here: Phibro Benefits. Phibro is an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, national origin, gender, age, religion, disability, sexual orientation, gender identity, veteran status, marital status or any other characteristics protected by law. Business Unit: Animal Health & Mineral Nutrition Division: Animal Health & Nutrition Department: Quality Location: US - Chicago Heights, IL Work Schedule: Monday - Friday (Standard Work hours)

We are seeking a dedicated QC Raw Materials Scientist III to act as a Subject Matter Expert for compendial raw material HPLC method verification and SOP generation. Your role will be integral in ensuring laboratory safety and compliance with environmental health and safety (EHS) standards. You will conduct compendial GMP testing in an analytical laboratory environment, utilizing a variety of wet chemistry and equipment-based assays. Your keen attention to detail will help you recognize and report out-of-specification or out-of-trend results to laboratory management, and you will recommend solutions to rectify any issues. PAY - $38 - $43 Responsibilities + Act as a Subject Matter Expert for compendial raw material HPLC method verification and SOP generation. + Demonstrate proper laboratory safety and housekeeping practices through weekly 5S Lab audits and monthly laboratory inspections. + Assure all activities meet EHS requirements. + Conduct compendial GMP testing in an analytical laboratory environment using a variety of wet chemistry and equipment-based assays. + Recognize and report out-of-specification/out-of-trend results to laboratory management and recommend solutions. + Maintain and troubleshoot analytical instrumentation and workspace as needed. + Perform method validation and/or qualification testing as needed. + Author and/or review SOPs and test method forms in the document management system eDMS. + Perform all duties in compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines. + Work with internal and external customers to ensure clear and open communication is maintained when resolving and raising issues. Essential Skills + Minimum of 5 years of pharmaceutical HPLC/UPLC experience. + Experience with compendial HPLC assays. + Knowledge of GMP regulations in a cGMP manufacturing environment. + Working knowledge of scientific principles for a wide range of analytical techniques. + Attention to detail and familiarity with compendia and USP methods. Additional Skills & Qualifications + BS Degree in a related field. + Prior use of EMPOWER is preferred. + Experience with ICP testing is preferred. + Experience in biopharmaceutical quality control. Work Environment The work schedule is Monday to Friday, from 8:00 am to 4:30 pm. The environment fosters impactful work, innovative thinking, and a customer-focused culture. You will be part of a fast-growing, global organization with a commitment to serving science and providing resources and opportunities for career growth. The role does not require weekend work. Job Type & Location This is a Contract to Hire position based out of Granite City, IL. Pay and Benefits The pay range for this position is $38.00 - $43.00/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 Granite City,IL. Application Deadline This position is anticipated to close on Jan 20, 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 due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

You will be responsible for in-process and release testing of Injectable pharmaceutical finished products produced on site. The chemist participates in the development of new procedures and is involved in validation studies as they pertain to analytical testing. Work is technical and specialized, requiring accuracy and attention to detail. Our Pharmaceutical Diagnostics (PDx) business is the number one global supplier of contrast media and molecular imaging agents used to enhance medical imaging exams. Used throughout all major disease area diagnostic and treatment pathways, PDx products support three patients every second around the world. Job Description Key responsibilities/essential functions: * Performs required analytical testing on in-process and final products. * Testing using HPLC, FTIR, ICP-OES, UV/VIS, Liquid Scintillation, and Gamma Spectrometer. * Participates in the performance of investigations of OOS results. * Tracking and trending of analytical data. * Participates in validation projects requiring analytical support. * Contributes to process improvement through Lean and 5S. * Assists in the stocking and supplying of the QC lab. * Performs visual inspection of finished product. Quality Specific Goals: * Knowledge and understanding of acceptance activity requirements for incoming, in-process, and final inspection requirements (as associated with job type/position) to ensure the product conforms to its specification and out of specification items are properly handled. * Basic knowledge and understanding of Stop Orders, Concessions, CAPA, Calibration, Preventative Maintenance, Material Identification & Segregation, documentation configuration control practices; documentation & disposition of non-conforming material, and Good Documentation Practices requirements, Part 11 compliance as associated with this job type/position * Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position * Complete all planned Quality & Compliance training within the defined deadlines * Identify and report any quality or compliance concerns and take immediate corrective action as required Required Qualifications: * Bachelor's degree in chemistry (preferred) or related science field. * Proficient with software applications applicable to the job. * Must be available for nights and weekends as needed. * Must have the ability to distinguish color. * Ability to lift 25lbs * Legal authorization to work in the U.S. is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening. Preferred Qualifications: * Waters Empower Experience or similar software. * Equipment experience with HPLC, ICP, UV/Vis, FT-IR. * Experience working with radioactive material including the use of gamma spectrometers, Ion Chambers and liquid scintillation analyzers. * Visual inspection experience Working knowledge of USP Experience in a FDA regulated QC environment Background in Math or Chemistry We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership - always with unyielding integrity. Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you'd expect from an organization with global strength and scale, and you'll be surrounded by career opportunities in a culture that fosters care, collaboration and support. We will not sponsor individuals for employment visas, now or in the future, for this job opening. For U.S. based positions only, the pay range for this position is $52,400.00-$78,600.00 Annual. It is not typical for an individual to be hired at or near the top of the pay range and compensation decisions are dependent on the facts and circumstances of each case. The specific compensation offered to a candidate may be influenced by a variety of factors including skills, qualifications, experience and location. In addition, this position may also be eligible to earn performance based incentive compensation, which may include cash bonus(es) and/or long term incentives (LTI). GE HealthCare offers a competitive benefits package, including not but limited to medical, dental, vision, paid time off, a 401(k) plan with employee and company contribution opportunities, life, disability, and accident insurance, and tuition reimbursement. Additional Information GE HealthCare offers a great work environment, professional development, challenging careers, and competitive compensation. GE HealthCare is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. GE HealthCare will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable). While GE HealthCare does not currently require U.S. employees to be vaccinated against COVID-19, some GE HealthCare customers have vaccination mandates that may apply to certain GE HealthCare employees. Relocation Assistance Provided: No

About Phibro Animal Health Corporation Phibro Animal Health Corporation is a publicly traded, global organization with a rich history in animal health and nutrition as a manufacturer and marketer of medicated feed additives, vaccines, nutritional specialty products, and mineral nutrition. We strive to be a trusted partner with livestock producers, farmers, veterinarians, and consumers who raise or care for farm and companion animals by providing solutions to help them maintain and enhance the health of their animals. Phibro is a diversified company in manufacturing and marketing products for ethanol performance, microbials for plants, home and industrial applications, and specialty chemicals for various industrial markets. In addition to, Phibro's revenues are in excess of $1 billion and are supported by over 2,400 employees worldwide. At Phibro, people are our greatest asset. We strive to develop a diverse workforce that fosters an environment where people feel supported in openly sharing their creativity and skills that allows them to be the most successful that they can be. If you are interested in working for Phibro and feel that you do not meet all qualifications, we encourage you to apply as you might be the right candidate for this role or other positions. The Laboratory Analyst is an integral part of our Laboratory Services team based out of our US - Quincy, IL - North Plant site. Hourly rate range for this position is $25.00 - $35.00 Position Purpose Performs qualitative and quantitative analyses of organic compounds and biologics to determine chemical and physical properties in support of Phibro Animal Health manufacturing facilities, Universal Testing, and product development. Key Responsibilities * Maintain, follow, and monitor safety policies as recorded in the Chemical Hygiene Plan and all Standard Operating Procedures. * Maintain good housekeeping practices for laboratory safety. * Report any safety infraction and take the appropriate action in accordance with the standard operating procedures. * Performs analysis on organic compounds and biologics including but not limited to proximate and vitamin analysis * Records weights, results and observations. * Assists with investigations related to out-of-specific ingredients/products or low-performing assays. * Works as primary operator on an instrument, capable of performing routine and non-routine maintenance as well as troubleshooting * Communicate with instrument companies/field engineers when needed for troubleshooting. * Takes point on ensuring all samples get analyzed for their assigned instrument and perform basic data review on routine QC samples. * Performs analysis for method validations or lab investigations * Assist in sample log-in, sample requests, or sending samples for analysis. * Works to maintain lab cleanliness including washing glassware and disposing samples. Competencies Technical / Operational / Personal * Experience with vitamin analysis * Proficient with HPLC analysis required * Experience with GC-MS preferred * ISO 17025 lab experience preferred * Attention to detail and accuracy. * Ability to coordinate multiple tasks, prioritize workload, and effectively accomplish goals. * Ability to effectively communicate (interpersonal, written and presentation) with internal and external individuals. * Ability to work independently or as a team member. Education and Additional Requirements Minimum associate degree in chemistry or science related field and 5 years of experience or bachelor's degree in a chemistry or science related field Preferred B.S with 2 years experience in HPLC vitamin analysis. To learn more about Phibro Animal Health's competitive benefits package, please click here: Phibro Benefits. Phibro is an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, national origin, gender, age, religion, disability, sexual orientation, gender identity, veteran status, marital status or any other characteristics protected by law. Business Unit: Animal Health & Mineral Nutrition Division: Animal Health & Nutrition Department: Laboratory Services Location: US - Quincy, IL - North Plant Work Schedule: Monday - Friday (Standard Work hours)

Job Title: Research Scientist Reporting: Director of Innovation Ascent Industries Co. is seeking a Research Scientist to join our Research and Development team. This role will serve as the technical focal point for new custom and contract manufacturing projects and drive successful execution from proof of concept through commercial-scale production. This role will collaborate with cross-functional stakeholders in R&D, Sales, Marketing, Engineering, and Manufacturing to drive commercial success with a focus on speed to solution, commercial-scale viability, deep technical rigor, and a proactive safety mindset. The ideal candidate combines strong technical skills in experiment design, synthesis, process chemistry, commercial-scale unit operations, and scale up within the chemicals or materials industry. This role is expected to serve as the subject matter expert for all analytical testing related to the contract manufacturing projects, implementing customer specified tests and introducing new test methods that are critical for ensuring product quality. Duties and Responsibilities: Serve as the technical focal point for new contract manufacturing opportunities. Identify fastest and most efficient route to commercial scale solutions for new contract manufacturing opportunities based on a deep understanding of process chemistry and plant unit operations. Design experiments based on sound scientific principles and statistical methods to validate technical packages for proof of concept, optimize processes, and develop technical package for manufacturing to support First Time in Spec production. Rapidly produce samples for customer evaluation based on a thorough understanding of plant equipment capabilities and technical requirements Establish R&D lab capabilities for synthesis, process development, sample preparation, and testing by evaluating current capabilities and additional needs to support project pipeline. Demonstrate expertise in a broad array of analytical instruments and drive new method development to align internal test methods and capabilities with customer methods and protocols. Leverage external labs for specialized test capabilities. Collaborate with key stakeholders in Sales, Engineering, Manufacturing, Procurement, and Product stewardship to drive successful commercialization. Engage with customers to gather process details, develop experimental plans, communicate project progress, present key findings, results, and support successful qualifications. Create Standard Operating Procedures and Work Instructions for core lab activities. Assure safe lab operations and compliance with site regulations while ensuring zero recordables. Skills, Qualifications, Experience, Special Physical Requirements: Ph.D. or master's degree in chemistry, Chemical Engineering, or Materials Science and Engineering Proven hands-on product development and industrial scale-up (3+ years) in specialty chemicals or materials industry with subject matter expertise in on or product categories: Surfactants, Emulsions, Dispersions, Specialty Additives, Acrylic Adhesives, and Reactive Blends. Know-how of product requirements for one or more market segments: Oil and Gas Chemicals, Water Treatment Chemicals, Personal Care, Lubricants, and CASE. Strong lab scale synthesis skills, working knowledge of commercial-scale process equipment, and prior experience scaling a product from the laboratory scale through robust commercial scale production. Solid understanding of interplay between raw materials, formulations, manufacturing process variables, product specifications, and product performance. Prior experience with development of detailed technical packages for scale up. In depth analytical and method development experience with techniques such as GPC, GC, HPLC, FTIR, NMR, Rheology, Particle Size, and wet chemistry. Design of Experiments and Six Sigma Green Belt Experience Preferred. Ability to prioritize tasks, manage multiple projects simultaneously, and meet tight deadlines. Strong communication skills both written and verbal. Success Metrics On time execution of R&D work for new contract manufacturing projects per milestones established in NPD process Improve technology transfer from lab to plant with a focus on developing detailed technical packages for achieving target specifications in the first production run. Develop detailed understanding of customer technical protocols for testing and drive quick internal implementation Serve as a technical interface to provide outstanding customer engagement in all technical aspects and help position R&D as our unique value proposition to contract manufacturing customers

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Assists in coordinating and delegating laboratory testing by setting priorities based on the needs of operations. Tests materials as assigned by priority listing provided daily by QC management using various types of equipment - pH meter, FTIR, HPLC, GC, HPTLC, ICP-MS, ICP-OES, LC/MS, GC/MS, LC/MS TOF, auto titrators, and balances. Independently sets up, runs, and troubleshoots instrumentation. Performs data interpretation and reporting. Revises and creates SOPs as needed. Provides guidance, mentoring and training to other technicians. Assists and conducts method transfers and method validation in coordination with methods group. Assists in coordination of the workload in lab including stability, raw materials, finished product, and special requests. Records and evaluates data and documentation for completeness. Initiates out-of-spec investigations. Performs various housekeeping duties in the lab including disposing of hazardous waste and instrument PM and calibrations. Complies with safety and GMP requirements. SAFETY RESPONSIBILITY STATEMENT Supports a culture of safe laboratory operations; follows all safety rules and procedures. Actively participates in the safety program by: engaging in training activities to learn what constitutes a safety hazard; reporting safety concerns to management or safety teams, submitting safety suggestions, and correcting or reporting to the appropriate people when the employee sees a workplace health or safety hazard, until it is resolved. Assists with communicating safety information to new employees. Fulfills responsibilities as outlined in the company safety management plan. QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions. EDUCATION and/or EXPERIENCE Bachelor's degree (B.S.) or equivalent from four-year college or technical school in a laboratory science such as Biology, Chemistry or related field, and at least five years laboratory experience including hands on instrumental analysis (such as FTIR, FT-NIR, HPLC, LC/MS, HPTLC, GC, GC/MS, ICP/MS, ICP/OES and UV/Vis), troubleshooting, and training experience. Familiarity with general laboratory safety, procedures and instrumentation. Excellent computer skills required, including Microsoft Word, Access and Excel. Experience with database management systems such as Oracle and LIMS are desired. Knowledge and application of cGMP regulations. Knowledge of industry quality control procedures, chemical laboratory instrumentation and standard operating procedures required. LANGUAGE SKILLS Ability to read and interpret documents such as product specifications, departmental instructions, and procedure manuals. Able to communicate effectively verbally and in writing. MATHEMATICAL SKILLS Ability to apply concepts such as fractions, percentages, averages, ratios, proportions, and the metric system to practical situations. REASONING ABILITY Excellent problem solving skills required. Able to compare results obtained to specifications to determine if result meets requirements. Ability to interpret a variety of instructions. OTHER SKILLS AND ABILITIES Excellent time management, meeting deadlines, attention to detail, verbal and written communication skills, listening, decision-making, troubleshooting/problem solving and organization skills required. Must possess strong organizational and leadership skills, be a self-starter and able to handle multiple tasks. Must possess professional attitude and be able to work well with peers and management. Ability to mentor and train lower level chemists. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of the job, the employee is required to be able to use hands to finger, handle or feel, reach with hands and arms to properly handle and prepare samples and materials in the lab as needed. The employee is regularly required to handle testing equipment, raw materials and finished product, tools, or controls and communicate in person and on the telephone. Repetitive proper handling and manipulation of the tools, instruments and materials during required procedures in preparation of samples are frequently required. In addition, computer keyboard and mouse usage is frequently required. The employee frequently is required to use his/her sense of taste or smell; to reach overhead; and to push/pull and move gas cylinders and 55 gallon drums at waist level. The employee is occasionally required to move from place to place within the facility, to climb, balance, or stoop. The employee must occasionally lift and/or move up to 10 pounds. Specific vision abilities required by this job include close vision and color vision. WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The employee is frequently exposed to vapors and/or herbal aromas. The noise level in the work environment is usually moderate. The employee may be exposed to potentially hazardous chemicals and biological materials. This position works in all areas of NOW's manufacturing facilities with direct exposure to ingredients (powders and liquids), mixes (powders and liquids), equipment, and packaging. 2025 BENEFITS AT A GLANCE

Job Description About Verdant Specialty Solutions Verdant Specialty Solutions is a dynamic, innovation-driven specialty chemicals company with a global footprint. Born from the McIntyre Group of the 1970s and relaunched in 2021, Verdant combines the agility of a small business with the safety, reliability, and scale of a larger organization, offering personal attention backed by industry-leading manufacturing and technical capabilities. With over 375 product offerings, nine strategic sites across the U.S. and Europe, and a steadfast commitment to sustainability, compliance, and customer-centric solutions, Verdant brings functional chemistry to life safely, reliably, and responsively. Are you a hands-on chemist who loves ensuring quality, safety, and operational excellence? Verdant Specialty Solutions, a global specialty chemical company serving world-leading consumer, industrial, and energy brands, is looking for a Quality Control Chemist to join our University Park team. Why this role is exciting: Play a key role in a fast-growing, start-up-like environment with global impact Work with cutting-edge specialty surfactant chemistries for top-tier clients Contribute directly to safety, quality, and operational excellence across multiple sites Opportunities to grow professionally in a collaborative, innovative culture What you will do: Perform in-process, final product, and raw material analyses Certify products for shipment and maintain accurate lab records Collaborate with operators, engineers, and QC colleagues to optimize processes Participate in process improvements, investigations, and quality initiatives Maintain compliance with ISO 9001, EFfCI, GMP, RSPO, and HSSE standards Operate lab systems (SAP) to track data, generate certificates, and manage inventories Requirements What we are looking for: Bachelor's degree in Chemistry, Chemical Engineering, Biology, or equivalent lab experience Knowledge of wet and instrumental analyses, lab safety, and solution prep Strong communication, attention to detail, and problem-solving skills Ability to work independently and collaborate with cross-functional teams Commitment to safety, quality, and compliance GC, HPLC, IR, Karl Fischer, and micro lab experience is a plus We have a steep learning curve, and the right candidate will need to know we are in a fast-paced manufacturing environment. Key Considerations: Union position Work Schedule: Enjoy a steady rotating 12-hour shift schedule that gives you built-in long weekends and extended time off every other week. Week 1: Monday, Tuesday, Friday, Saturday (48 hours) Week 2: Sunday, Wednesday, Thursday (36 hours) Shifts rotate between days and nights about every 10 weeks, offering variety and balance. This isn't just a QC role, it's your opportunity to shape quality, drive innovation, and grow your career in a global specialty chemicals company. Benefits Why you'll love it here: Competitive base pay ($24.75/hr.), bonus potential. Comprehensive benefits package including health, dental, vision, retirement savings, and generous PTO. Career growth opportunities in a dynamic, expanding business. Our trainees typically see rapid development: many move from “C” Chemist to “B” Chemist in about 3 months, and by around 9 months are often working at or near the “A” Chemist level. While the pace of growth depends on the individual, those who reach “A” Chemist generally master all key testing procedures and gain hands-on experience with our most common products, building a strong foundation for continued advancement. Ready to make your next move? Apply today and let's win together. EOE AA M/F/Vets/Disabled Benefit Summary