Quality control analyst jobs in Des Plaines, IL

Our client, a leader in pharmaceutical manufacturing, is looking to hire an entry level Chemist to join their team! Pay Rate: $19-20/hr Hours: 1shift shift 8a-4:30p M-F Terms: contract-to-hire This candidate will be responsible for assisting with laboratory experiments, analyzing chemical compounds, preparing solutions, and maintaining equipment under the supervision of senior chemists. Key responsibilities include recording and interpreting data, ensuring quality control, and adhering to safety protocols. Core responsibilities Perform laboratory procedures: Conduct experiments, prepare chemical solutions and reagents, and analyze substances to determine their composition and concentration. Analyze data: Test materials to ensure they meet quality and safety standards and interpret experimental results. Maintain equipment: Set up, calibrate, and maintain laboratory equipment. Document findings: Record data, write technical reports, and maintain detailed lab notebooks. Ensure safety: Follow established procedures and safety protocols to maintain a safe laboratory environment. Support senior staff: Assist senior chemists and researchers with projects, which can include method development and quality control. Essential skills and qualifications A bachelor's or master's degree in chemistry. A strong foundation in chemistry principles and laboratory techniques. Proficiency in data analysis, including relevant software. Excellent attention to detail and problem-solving abilities. Strong communication skills for reporting and collaboration. Familiarity with common laboratory equipment and safety protocols.

Ready to revolutionize flexible packaging technology with cutting-edge UV and EB liquid formulations? Pave Talent is hiring on behalf of our client - an established mid-size chemical manufacturer with multiple locations, known for their collaborative, innovation-driven, and safety-first culture. This industry leader is the third largest ink producer in North America, with 12+ years average employee tenure and tremendous growth in flexible packaging solutions. As an R&D Chemist - UV/EB Liquid Specialist, you'll drive breakthrough innovations in UV Flexographic and Screen Ink technologies while supporting a $100M+ business unit experiencing unprecedented growth. Your formulation expertise will directly impact cost-savings initiatives and customer satisfaction across commercial and packaging applications. Your Impact: Troubleshoot complex technical challenges with existing UV/EB technologies while providing rapid customer support solutions Develop next-generation UV Flexo and Screen Ink technologies tailored to evolving customer specifications and market demands Lead EB Liquid formulation projects and UV/EB Coatings development for emerging packaging applications Evaluate and optimize raw materials to achieve 15-20% cost-savings opportunities through strategic formulation improvements Provide critical technical manufacturing support, ensuring seamless scale-up from lab to production environment Author comprehensive project reports and technical documentation for sales teams and direct customer presentations Maintain state-of-the-art laboratory equipment and analytical instrumentation for optimal research productivity What You Bring: Required: Bachelor's degree in Chemistry, Chemical Engineering, or equivalent technical discipline 5+ years hands-on experience in ink and coating formulation with measurable product development success Proven UV/EB liquid ink formulation expertise with understanding of photopolymerization chemistry Advanced mathematical and analytical skills with proficiency in statistical analysis and data interpretation Exceptional technical writing abilities and strong verbal communication for customer-facing interactions Meticulous record-keeping skills with experience in regulated laboratory environments Preferred: Direct UV/EB Liquid Ink and Coatings application experience in packaging or commercial printing SAP or similar ERP system experience for materials management and project tracking Six Sigma or lean manufacturing methodology knowledge Why This Opportunity Stands Out: Market-competitive salary range $85K-$100K with performance bonus structure, comprehensive benefits from Day 1 including medical/dental/vision, 401(k) with company match, paid volunteer time off, and parental leave. Join a team where 1/3 of chemists have 15+ years experience, working in an autonomous environment with cutting-edge analytical equipment and significant opportunities for professional growth in sustainable chemistry innovation. Work alongside a close-knit R&D team that values creative problem-solving and celebrates breakthrough innovations in environmentally conscious ink technology. This is your chance to shape the future of flexible packaging while building a career with an industry leader committed to employee development and retention. Ready to make your mark in sustainable chemistry innovation? Apply via LinkedIn and Pave Talent will contact qualified candidates immediately. Confidential search - your application is fully private. Apply now!

Job Posting Start Date 11-19-2025 Job Posting End Date 12-22-2025Flex is the diversified manufacturing partner of choice that helps market-leading brands design, build and deliver innovative products that improve the world.A career at Flex offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but don't meet every bullet point, we encourage you to apply and join us to create the extraordinary.Job Summary To support our extraordinary teams who build great products and contribute to our growth, we're looking to add a Quality Control Inspector located in Buffalo Grove, IL Reporting to the manager the potential candidate would inspect electronic systems, assemblies, subassemblies, components and parts for conformance to specifications. 0600am-0600pm Rotating Shift Responsibilities: Performs visual inspection of electronic card and sub-assemblies, and systems or units to ensure that all product meets the established specifications for reliability and workmanship. Utilizes gages, templates, microscopes and other manufacturing aids to ensure that all product meets the established specifications for reliability and workmanship. Ensures that all required process operations have been performed on the product that is being inspected. Enters all quality data into the appropriate electronic or manual systems. Notifies the appropriate personnel if unusual product defects are identified or if process falls below acceptable levels. Provides timely feedback to manufacturing if non-conforming product is identified. Accurately completes all administrative activities associated with quality inspection. Performs process audits and assists manufacturing with the interpretation of the quality and workmanship standards. Assists with the disposition of all non-conforming materials/product. Qualifications: Completion of a high school degree or equivalent is preferred. Successful completion of company provided training may be required. Typically requires 1year of related experience. AW20 What you'll receive for the great work you provide: Full range of medical, dental, and vision plans Life Insurance Short-term and Long-term Disability Matching 401(k) Contributions Vacation and Paid Sick Time Tuition Reimbursement Pay Range (Applicable to Illinois)$17.98 USD - $24.27 USD HourlyJob CategoryQuality Is Sponsorship Available? NoFlex is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. We do not discriminate based on: age, race, religion, color, sex, national origin, marital status, sexual orientation, gender identity, veteran status, disability, pregnancy status, or any other status protected by law. We're happy to provide reasonable accommodations to those with a disability for assistance in the application process. Please email accessibility@flex.com and we'll discuss your specific situation and next steps (NOTE: this email does not accept or consider resumes or applications. This is only for disability assistance. To be considered for a position at Flex, you must complete the application process first).

Bell Flavors & Fragrances, Inc. is seeking a dedicated and detail-oriented Quality Control Technician to join our team. The Quality Control Technician will be responsible for ensuring that all raw materials and finished products meet established standards and regulatory requirements. This role involves performing organoleptic (sensory) evaluations, analytical testing, and documentation to support consistent quality and safety. Key Responsibilities: Conduct organoleptic (sensory) evaluations of flavor ingredients and finished products. Perform routine QC tests such as specific gravity, refractive index, pH, flashpoint analysis, particle size testing, Gas Chromatography, titration, and micro testing. Maintain accurate QC records, test results, and batch release documentation. Review Certificates of Analysis (COAs) and supplier documentation for compliance. Approve raw materials for use and finished products for shipment. Communicate quality deviations or non-conformances to Production and Quality teams promptly. Assist in investigations of non-conformances and implement corrective actions. Work closely with Production, R&D teams, vendors, and the Purchasing team to resolve quality issues. Assist customers with requests such as COA requests and shelf-life extension requests. Calibrate and maintain laboratory instruments. Follow all safety protocols and maintain a clean, organized lab environment. Qualifications: Associate or bachelor's degree in food science, Chemistry, or related field preferred. 1-3 years of experience in a food, beverage, or flavor manufacturing QC role. Understanding of FDA, USDA, GMP, and State Food Safety/Quality regulations. Knowledge of sensory evaluation techniques and food safety standards. Familiarity with laboratory testing methods, microbiology, and chemical analysis. Strong attention to detail, organizational, critical thinking, and communication skills. Ability to work collaboratively in a team environment with facilities, regulatory agencies, customers, and vendors. Proficient in Microsoft Office. Why Apply: Opportunity to work with the dedicated team. Collaborative work environment. Full-Time benefit package Competitive salary range $22 - $24 per hour. About Us: Bell Flavors & Fragrances, Inc. is a leading company in the flavor and fragrance industry, committed to providing high-quality products and services to our customers. Join our team and be part of a dynamic and innovative environment. *********************

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.

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Position Overview: Lilly is actively growing its manufacturing footprint globally to meet the needs of patients and deliver on our exciting future. As a result, Lilly is looking for experienced quality assurance associates to support our growth in Kenosha County, Wisconsin. This is an outstanding opportunity to deliver on new manufacturing investments and new pioneering technologies. The Senior Scientist, Quality Control - Equipment, is responsible for asset delivery and maintenance in the Quality Control Laboratory. This role requires an understanding of corporate quality systems, a detail-oriented quality mindset with an understanding of analytical/microbiology laboratory equipment, knowledge of lab methods to understand intended use of equipment and their failure modes and effects. The individual in this position must possess skills which include equipment troubleshooting, prioritization, written and oral communication, decision making, strong interpersonal/people management, computer applications, and problem-solving. Responsibilities: Maintains responsibility for a safe work environment, leading safety initiatives, and working safely; accountable for supporting all Health, Safety, and Environmental Corporate and Site Goals. Authors equipment qualification/validation protocols and strategies for the QC Laboratories. Provides support for equipment relocation and qualification associated with Lab master plans. Participates in data integrity by design, mitigation through controls and improvement initiatives. Executes technical review and execution of qualification/validation protocols. Recommends and specifies equipment purchases based on user requirements. Communicates with other functions and external vendors regarding qualification issues and key operational objectives. Acts as liaison between the maintenance team and laboratory personnel to schedule preventative and corrective maintenance of equipment. Applies knowledge of quality principles, cGMPs, regulations, corporate standards, practices and local procedures in the development of qualification/validation protocols and equipment lifecycle management. Interacts effectively with support groups and vendors. Networks with other areas to understand best practices and share knowledge to ensure customer needs are met. Identifies improvements and streamlines quality systems relating to equipment. Serves as equipment subject matter expert in the review of technical documents. Acts as subject matter expert and originator of change controls. Originates and investigates deviations in the QC laboratory. Multitasks, prioritizes, and coordinates work to meet laboratory's needs. Demonstrates problem solving and investigative skills. Makes decisions based on knowledge, experience, best practices and requirements. Works independently and accurately with minimal supervision. Performs routine maintenance and repairs. Basic Requirements: Bachelor's degree in a science, engineering, or pharmaceutical-related field of study or equivalent experience. Minimum 5 years in the pharmaceutical industry with specific Quality Control and laboratory equipment experience. On-site presence required. Additional Skills/Preferences: Fluent in English. Demonstrated understanding of cGMP regulations. Experience supporting laboratory equipment in a GMP environment, including ability to repair and maintain instruments Ability to manage and contribute to multiple concurrent project activities and adapt to changes in priorities. Understanding of compliance requirements and regulatory expectations for laboratory systems. Previous experience with managing data integrity regulations and controls. Working knowledge of CMMS, Kneat, Empower, TrackWise, LabVantage LIMS, Veeva. Deep understanding of compliance requirements and regulatory expectations Demonstrated accuracy and proficiency in analytical skills. Proficiency with computer systems including Microsoft Office products, LIMS, Laboratory Execution Systems, chromatography systems, electronic laboratory notebook systems including implementation of systems. Excellent written and oral communication skills Previous LEAN experience: ability to drive continuous improvement. Strong technical aptitude and ability to train and mentor others. Project management experience. Demonstrated problem-solving and decision-making capability. Demonstrated technical writing skills Understanding of statistical tools and analyses. Strong documentation skills and attention to detail. Demonstrated strong oral and written communication skills. Demonstrated interpersonal skills and the ability to work as a team. Root cause analysis/troubleshooting skills. Demonstrated attention to detail and ability to maintain quality systems. Proven ability to work independently or as part of a Team to resolve an issue. Previous regulatory inspection readiness and inspection execution experience. Additional Information: Primary location is Kenosha County, Wisconsin. Ability to travel (approximately 10%). Ability to work overtime as required. This is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the . For GMP purposes, the job description should be updated for significant changes. As always, you should consult with your supervisor regarding your actual job responsibilities and any related duties that may be required for the position. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $65,250 - $169,400 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

2nd Shift - 3:15 PM - 11:45 PM This position requires individual to have ability to perform wet chemistry and instrumentation testing as defined in Essential Job Functions and any other testing as assigned by the supervisor. Ability to understand the organization Stability Program and QMS Program. Ability to accept projects as assigned and ensuring on-time execution. The position requires individual to follow Standard Operating Procedure (SOP) and Good Laboratory Practices (GLP) as well as any applicable industry standards. Ability to understand company nonconformance SOP and assist with performing investigations to determine root cause under supervision. Ability to understand and perform calculations as required in BAP. Other essential job functions, responsibilities and requirements are listed below. ESSENTIAL JOB FUNCTIONS Capable of effective communication skills for interactions with laboratory colleagues, and colleagues from numerous functional areas. Capable of listening actively and readily assumes responsibility for actions. Ability to perform wet chemistry and instrumentation testing (HPLC, GC, IR, Karl Fisher, etc.) in a regulated environment by following procedures and/or USP testing procedures for finished products and raw materials samples. Ability to use Dishwasher, Balance Micropipette, LC, GC, IR, Auto-titrator, Oven, Viscometer, pH Meter. Ability to perform Water Determination, Visual Comparison, Package Integrity, Density, Refractive Index, pH, Organoleptic. Ability to understand "deals" associated with various markets. Ability to correctly associate "deals' to various PAR(s). Ability to read and understand USP-NF. Ability to understand and follow cGMP requirements. Ability to understand the organization Stability program/schedule for retrieval, testing and documentation of Monthly Samples. Ability to perform testing as assigned. Ability to use and have knowledge of the organization QMS program. Ability to launch packets in MC to revise PAR/RMS/BAP/FRM under minimum supervision. Ability to perform peer reviews or document reviews. Ability to accept projects as assigned. Ability to execute projects under supervision. Ability to understand and to perform calculations as required in BAPs and perform basic statistical calculations such as % Difference, Average, Standard Deviation, % RSD. Ability to understand the company nonconformance SOPs and assist with performing the investigations in determining root cause under supervision. ADDITIONAL RESPONSIBILITIES Performs special projects, as assigned by the Supervisor and/or Manager Quality Control, which enhance and contribute to the growth of the Quality Control Department. Performs and assumes other duties and responsibilities, as may be required by the Supervisor and/or Manager, Quality Control. Supports the Winner's Circle and Blistex Quality System processes. REQUIRED EDUCATION, EXPERIENCE AND SKILLS Bachelor's degree in Chemistry, Biology, or related scientific discipline with 0-1 years of applicable laboratory experience preferable in the cosmetics/pharmaceutical OTC industry. Complies with all safety standards while on Company premises and during performance of job functions. Computer literacy in a Windows environment is required. Familiarity with Excel, Word and/or Access Database is preferred. Must possess a good understanding of the safety standards and hazards associated with a Quality Control environment. High degree of familiarity with and ability to use office machines. Must be flexible to work 1st, 2nd, 3rd shift or a modified work shift, as departmental needs demand. Willingness to accept other duties, as assigned. Must be discreet with confidential information of which he/she has access. Must possess the ability to develop and maintain an effective working relationship with internal and external customers, function as a team player, accept constructive criticism from management, and comply with Company policies. Knowledge of computerized data acquisition and analysis systems, such as Waters Empower or PE Totalchrom is required. Must possess good oral and written communication skills in Business English (spelling, grammar, and punctuation, etc.). PHYSICAL DEMANDS & ENVIRONMENT This position requires the individual to stand, walk, stoop, kneel, bend or crawl, reach with hands and arms overhead, and taste or smell 33 to 66% of the time. This position requires the individual to sit, talk or listen, and use hands to finger, handle or feel 66 to 100% of the time. This position requires the individual to climb or balance up to 33% of the time. This position will require the individual to lift up to 25 pounds 33 to 66% of the time. The vision requirements for this position includes close vision (clear vision at 20 inches or less), distance vision (clear vision of 20 feet or more), color vision (ability to identify and distinguish colors), peripheral vision (ability to see up, down, left or right while eyes are fixed on a given point), depth perception (3-dimensional vision, ability to judge distances and spatial relationships), and ability to adjust focus (ability to adjust the eye to bring an object into sharp focus). This position has exposure to wet, humid conditions (non-weather), work near moving mechanical parts or vibration, fumes, or airborne particles, and toxic or caustic chemicals up to 33% of the time. The noise level for this position will be moderate noise (Ex: Business office with typewriters and/or computer printers, light foot traffic). The Personal Protective Equipment requirements that are used in this position is a hair net, beard net, safety glasses, cut resistant gloves, and fume hood.

The Quality Control Chemist II plays a critical role in ensuring the integrity and compliance of pharmaceutical or chemical products through advanced analytical testing. This position requires a minimum of 5 years of laboratory experience in analytical chemistry, with demonstrated expertise in High-Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC). The ideal candidate will be proficient in Empower chromatography data software, capable of performing complex analyses, and contributing to method development and troubleshooting. Working in a regulated environment, the QC Chemist II is responsible for executing and documenting analytical procedures in accordance with cGMP, USP, and ICH guidelines. This role supports product release, stability studies, and raw material qualification, while also participating in investigations and continuous improvement initiatives. Our Pharmaceutical Diagnostics (PDx) business is a global leader in imaging agents, used to improve and enhance the images that radiologists use to diagnose and monitor disease. We support healthcare professionals in the administration of neurology, cardiology and oncology procedures that are used to image three patients around the world, every second. Job Description Key Responsibilities: * Conduct routine and non-routine testing of raw materials, in-process samples, and finished products using HPLC, GC, UV-Vis, FTIR, and other analytical techniques. * Interpret and report analytical data in accordance with regulatory standards (e.g., cGMP, USP, ICH). * Utilize Empower software for method execution, data acquisition, processing, and reporting. * Perform method development, validation, and troubleshooting as needed. * Maintain accurate and complete laboratory records, including notebooks, logbooks, and electronic data systems. * Participate in investigations related to out-of-specification (OOS) results, deviations, and laboratory errors. * Support continuous improvement initiatives and contribute to SOP revisions and training documentation. * Ensure compliance with safety protocols and maintain a clean, organized laboratory environment. Required Qualifications: * Bachelor's or Master's degree in Chemistry, Biochemistry, or a related scientific field. * Minimum of 5 years of experience in a regulated analytical laboratory setting. * Strong proficiency in HPLC and GC, including method execution and troubleshooting. * Hands-on experience with Empower software for chromatographic data analysis. * Familiarity with regulatory requirements (FDA, cGMP, GLP). * Excellent attention to detail, documentation skills, and ability to work independently or in a team. 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 $61,336.00-$92,004.00 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

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.

! Weee! is the largest and fastest-growing ethnic e-grocer in the United States, operating in one of the largest underserved categories in retail with affordable access to exciting ethnic food. By partnering with local suppliers, redesigning the value chain and leveraging social buying, Weee! is reshaping the grocery business entirely. You can read more about us on Business Insider, Reuters and TechCrunch. Weee! is headquartered in Fremont, CA, and is currently available coast to coast with exceptional growth (5x YoY) across geographies, categories and ethnicities. We have raised $800M+ in funding to date from leading investors including Softbank Vision Funds, DST, Blackstone, Tiger Global, Lightspeed Ventures, Goodwater Capital, XVC and iFly. The opportunity now is to join a rocketship as we prepare for the next stage of growth, and an eventual public listing. This role is onsite 5 days a week in Hodgkin, IL About the Role The ICQA Specialist will be responsible for overall inventory accuracy and managing shrinkage , including investigating customer complaint cases related to the inventory issues within the Fulfillment Centers. The location will be in Hodgkin, IL Responsibilities: Monitor and improve inventory accuracy and ensure inventory count completeness Oversee physical inventories, cycle counts, and audit reconciliations Investigate inventory variances and assist in resolving/reducing discrepancies, Coordinate with cross-functional teams (e.g. receiving, merchandising, customer service, etc.) to resolve inventory issues. Monitor inventory key metrics and provide accurate and comprehensive inventory performance reports. Responsible for ensuring proper handling of problem products (e.g. ensuring correct inventory adjustments) Must have the ability to investigate discrepancies in the cooler / freezer . Qualifications: 2 years of experience in warehouse, logistics or manufacturing preferred Bachelor's Degree preferred Experience with warehouse operations or WMS systems preferred Experience in reporting and analyzing operational performance in order to implement recommendations Proven track record of driving continuous improvement Experience in analyzing problems, identifying alternative solutions and implementing recommendations Communicate clearly using excellent written and verbal skills Able to work well under pressure while managing competing demands and tight deadlines Experience with excel / google sheets is preferred. Benefits Comprehensive health insurance package, including medical, dental, and vision. PPO/HMO packages 401k, 4% company match Equity and Bonus Vacation, sick and holiday time off Monthly mobile stipend Monthly Weee! Points credits Compensation Range The US base salary range for this full-time position is $21 - $25 an hour This role may be eligible to discretionary bonus, incentives and benefits Our salary ranges are determined by role, level, and location The range displayed on each job posting reflects the minimum and maximum base salary for new hires for the position across all US locations. Within the range, individual pay is determined by multiple factors like job-related skills, experience and work locations. Your recruiter can share more about the specific salary range during the hiring process. Please note that the compensation details listed in US role postings reflect the base salary only, and do not include any variable compensation elements. Weee! is an equal opportunity employer welcoming all qualified applicants regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status or any other basis prohibited by law. Discrimination or harassment of any kind is not tolerated at Weee!. If you need to inquire about an accommodation or need assistance with completing the application, please email us at applicantaccommodation@sayweee.com . For more jobs and to find out more about Weee!, visit our career page: ********************************* Softbank Vision Funds

Job Description The Quality Control Chemist is responsible for daily lab testing with the purpose of accepting or rejecting test samples based on pre-determined specifications. The successful candidate will be able to work quickly and safely and will assist the Quality Control Manager with other tasks, as needed. ESSENTIAL DUTIES AND RESPONSIBILITIES Include the following. Other duties may be assigned. • Performs laboratory tests including pH, fluoride, viscosity, specific gravity, color, and appearance. • Tests raw materials, bulk intermediates, finished products and stability samples for specific quality attributes. • Uses and maintains HPLC, GC, FTIR, and other instruments. • Assists in performing method validations. • Performs a variety of wet lab techniques including but not limited to: titrations, pH, ISE, etc. • Writes and revises SOPs and tests methods as needed. • Follows documented procedures: SOPs, test methods, transfer protocols. • Prepares reports and reviews data. • Follows lab safety procedures. • Performs other tasks, as assigned. SUPERVISORY RESPONSIBILITIES None 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 may be made to enable individuals with disabilities to perform the essential functions. EDUCATION and/or EXPERIENCE Bachelors of Science in Chemistry. LANGUAGE SKILLS Able to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations. MATHEMATICAL SKILLS Able to calculate figures and amounts such as proportions, percentages, area, circumference and volume. Able to apply concepts of basic algebra and geometry. REASONING ABILITY Able to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. Able to deal with problems involving several concrete variables in standardized situations. 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. Specific vision abilities required by this job include close vision and depth perception. 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.

Job Description Title: Quality Supervisor Job Type: Full-time | On-site | Mount Prospect Radienz Living is a leading North American manufacturer of home and personal care products, such as unit dose, all-purpose cleaners. The company provides customers with private label solutions and contract manufacturing services for products found in retail and institutional markets. Radienz Living is passionate about providing its customers with exceptional manufacturing capabilities through its commitment to agility in innovation, trust and reliability, and sustainable creation that supports a cleaner way of living. Through acquisition, the company expanded into liquids products, unit dose packaging for dish, laundry, and other home care products, including detergents, fabric softeners and other cleaners. Throughout the years, the company has built robust quality systems, multiple GMP certifications, and in-house FDA/EPA microbiology, quality control, chemistry, and R&D labs. Background: The Quality Supervisor works in a supervisory role in all quality activities. The Supervisor reports to the Quality Manager and supervises QC Technicians. This position ensures safety standards are being upheld and GMP and GLP are followed. Responsibilities: This position is a working supervisor that oversees daily QC inspections and in-process testing. Implementation of Quality In-Process Inspection (QAPI) programs in accordance with ISO and GMP guidelines. Develops, establishes, and validates routine in-process testing methods and procedures. Manages quality workload and work of technicians across 1st, 2nd and 3rd shifts. Supervise QC Technicians and ensure training for the team is updated. Review and approve reports. Facilitates nonconforming product, OOS investigations, and CAPA investigations. Maintains in-process and receiving inspection, test equipment calibration program. Collaborate with manufacturing and engineering teams to establish and verify critical process parameters and problem-solving activities. Maintain the quality control program together with Production and Operations. Provides QC inspection trends and weekly reports to Quality Manager. Ensure adherence to company quality standards, policies, and procedures. Work closely with production, QA, and QS teams to ensure product quality and customer satisfaction. Provide support for Bensenville operations and other facilities when required. Stand in for the Quality Manager and other QC Techs when they are unavailable. Qualifications: Associate or bachelor's degree with a background or at least 5 years' experience in QA/QC. Required Experience: Five+ (5) years' experience in quality assurance/quality control in pharmaceutical, food, medical device or manufacturing of detergent industry preferred. Strong leadership and training skills. Knowledge of GMP, ISO and related guidance documents. Knowledge of Statistical Sampling Plans and Methods including AQL Inspection Method Knowledge of Statistical Process Control Methods including process capability and control charting. Strong communication skills required. Works with all levels of employees. Strong attention to detail required. Project management skills. Proficient in troubleshooting QC equipment and processes. Strong communication, critical thinking, and problem-solving skills. Computer Skills - ERP Programs, Microsoft Excel, Word, Power Point, and Adobe Acrobat. Physical & Work Environment Requirements: Ability to work in a manufacturing/production environment. Ability to multitask. May require standing, walking, lifting, or operating QC equipment during shift. Flexibility to adjust schedule to meet departmental needs across shifts. Must be able to lift and carry a minimum of 20 lbs.

Job Description1st Shift Quality Control Schedule: 7:00 AM - 3:00 PM, Monday through Friday; Saturdays as needed Pay Rate: $18.00-$22.00 per hour Responsibilities Inspect incoming materials, assemblies, and finished installations for defects, damages, or missing parts. Verify walls, fixtures, and assemblies are installed according to drawings, measurements, and specifications. Use QC tracking tools (such as Smartsheet or logs) to record issues by project, store, or display. Assign corrective actions to the responsible team or individual. Take photos and detailed notes of defects or incomplete work. Flag issues on-site (red stickers, tags, or markings) to prevent project delays. Re-inspect corrected work to confirm compliance before final approval. Approve completed work with visible indicators (e.g., yellow stickers or QC tags). Communicate findings with project managers, leads, and team members. Ensure compliance with safety standards and company quality policies. Qualifications Previous experience in construction, carpentry, fixture installation, or manufacturing preferred. Strong attention to detail with ability to identify defects and deviations. Proficient with documentation tools (spreadsheets, Smartsheet, mobile QC apps). Ability to read blueprints, shop drawings, and installation guides. Good communication and teamwork skills. Problem-solving mindset with focus on continuous improvement. Contact Information To apply, please visit our website at Midwaystaffing.com or stop by our office located at: 1460 N Farnsworth Ave, Aurora, IL 60505You can also reach us by phone at 331-212-5187. When calling, ask for Claudia, or Jaime for more information.To ensure your application is processed quickly, please have your resume ready, as the position requires both a resume submission and an interview. We look forward to hearing from you!What We Offer Midway Staffing offers a comprehensive benefits package including: Medical Dental Vision Life/AD&D benefit options to all eligible employees About Midway Staffing Midway Staffing is a dynamic and rapidly growing enterprise dedicated to connecting top talent with leading organizations. Specializing in innovative staffing solutions, we are committed to delivering exceptional service to both clients and candidates.With a strong presence spanning multiple locations nationwide and recognition on the prestigious Inc. 5000 list of Fastest-Growing Private Companies in America from 2019 to 2024, Midway Staffing exemplifies excellence and growth.We are equally dedicated to fostering internal development and supporting career advancement opportunities for our team members.

We are seeking a skilled QC Chemist to perform wet chemistry testing on raw materials, including IR Spectroscopy, melting point temperature, and viscosity, while adhering to USP methodology. Responsibilities * Run identification tests like Thin Layer Chromatography and spectroscopic tests. * Perform limit tests for things like chlorides, sulfates, heavy metals, elemental impurities, and aluminum. * Carry out other tests and assays such as Karl Fischer, acid value, saponification value, iodine value, hydroxyl value, peroxide value, and oil-related assays. * Perform physical tests like viscosity, melting point, congealing temperature, and mid-IR and UV-Vis analysis. * Work with lab instruments like refractometers, densitometers, pH meters, auto-titrators, UV-Vis spectrophotometers, and FTIR. Essential Skills * Bachelor's Degree in Chemistry. * 1-3 years of experience in a GMP/regulated laboratory setting. * Familiarity with raw material testing. About Actalent Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021. Diversity, Equity & Inclusion At Actalent, Diversity And Inclusion Are a Bridge Towards The Equity And Success Of Our People. DE&I Are Embedded Into Our Culture Through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people Job Type & Location This is a Contract position based out of Downers Grove, IL. Pay and Benefits The pay range for this position is $25.00 - $25.00/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 Downers Grove,IL. Application Deadline This position is anticipated to close on Dec 12, 2025. 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 for other accommodation options.

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 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 - $25.00 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 Accountable Accepting Direction Attendance and Punctuality Attentive Listening Collaborative Communicating Effectively Critical Thinking Delivering High Quality Work Demonstrating Initiative Detailed Oriented Displaying Technical Expertise Following Policies and Procedures Interacting with People at Different Levels Managing Time Prioritizing and Organizing Work Problem Solving Working Safely Technical 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 Skills Proven 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)

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 - $25.00 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)

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

The Laboratory Technician I position has the primary responsibility to assist in all essential functions required for the Chemistry Group. ● Laboratory Technician I will report directly to the Chemistry Group Lead ● This position has no supervisory responsibilities. Essential Functions ● Ensures safe working conditions in the laboratory and offices, and supports Phigenics safety team objectives ● Has a general understanding of all Phigenics Analytical Services Laboratory (PASL) offerings and operations ● Understand and follow Standard Operating Procedures (SOPs) for the Chemistry Group. ● Receive and log chemistry samples ● Prepare materials for chemistry sample processing under direct supervision ● Process chemistry samples according to SOPs under direct supervision ● Record sample location data and results in the laboratory database ● Communicates with clients and the sales team to ensure accurate sample processing ● Perform quality control and quality assurance procedures; and maintain quality system records to comply with all accrediting agencies ● Assist with the receipt, inspection, and stocking of supplies ● Performs lab maintenance, including, but not limited to: - Clean lab equipment and wash glassware and vials - Clean and store materials used for testing ● Discard old chemistry samples ● All tasks require exercise of discretion and independent judgment in important scientific laboratory procedures and operations ● Performs additional tasks as assigned by the Chemistry Group Lead. Position Requirements ● 4-year chemistry degree or equivalent experience in chemistry or a minimum of 2 years experience in a relevant laboratory setting ● Strong time management skills ● Strong verbal & written skills ● Attention to detail ● Ability to work overtime frequently, sometimes with little or no notice. ● Ability to work with potentially sensitive biological or chemical ingredients ● Knowledgeable in the use of computers - MS Word, Excel, PowerPoint; LIMS Accountabilities ● Safety is our priority. No accident is acceptable ● Follow laboratory SOPs for preparing and processing chemistry samples ● Provide accurate sample analysis results and reports ● Ensure quality control and assurance is maintained ● Maintain logs and records accurately ● Perform laboratory maintenance tasks accurately and in a timely manner ● Receive, inspect, and stock supplies in a timely manner 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. Phigenics LLC is an Equal Opportunity Employer that does not discriminate based on actual or perceived race, creed, color, religion, alien status, age or national origin, ancestry, citizenship status, age, disability or handicap, sex, marital status, veteran status, sexual orientation, arrest record, or any other characteristic protected by applicable federal, state or local laws. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States, and to complete the required employment eligibility verification form upon hire.

Job Description 2nd Shift - 3:15 PM - 11:45 PM This position requires individual to have ability to perform wet chemistry and instrumentation testing as defined in Essential Job Functions and any other testing as assigned by the supervisor. Ability to understand the organization Stability Program and QMS Program. Ability to accept projects as assigned and ensuring on-time execution. The position requires individual to follow Standard Operating Procedure (SOP) and Good Laboratory Practices (GLP) as well as any applicable industry standards. Ability to understand company nonconformance SOP and assist with performing investigations to determine root cause under supervision. Ability to understand and perform calculations as required in BAP. Other essential job functions, responsibilities and requirements are listed below. ESSENTIAL JOB FUNCTIONS Capable of effective communication skills for interactions with laboratory colleagues, and colleagues from numerous functional areas. Capable of listening actively and readily assumes responsibility for actions. Ability to perform wet chemistry and instrumentation testing (HPLC, GC, IR, Karl Fisher, etc.) in a regulated environment by following procedures and/or USP testing procedures for finished products and raw materials samples. Ability to use Dishwasher, Balance Micropipette, LC, GC, IR, Auto-titrator, Oven, Viscometer, pH Meter. Ability to perform Water Determination, Visual Comparison, Package Integrity, Density, Refractive Index, pH, Organoleptic. Ability to understand "deals" associated with various markets. Ability to correctly associate "deals' to various PAR(s). Ability to read and understand USP-NF. Ability to understand and follow cGMP requirements. Ability to understand the organization Stability program/schedule for retrieval, testing and documentation of Monthly Samples. Ability to perform testing as assigned. Ability to use and have knowledge of the organization QMS program. Ability to launch packets in MC to revise PAR/RMS/BAP/FRM under minimum supervision. Ability to perform peer reviews or document reviews. Ability to accept projects as assigned. Ability to execute projects under supervision. Ability to understand and to perform calculations as required in BAPs and perform basic statistical calculations such as % Difference, Average, Standard Deviation, % RSD. Ability to understand the company nonconformance SOPs and assist with performing the investigations in determining root cause under supervision. ADDITIONAL RESPONSIBILITIES Performs special projects, as assigned by the Supervisor and/or Manager Quality Control, which enhance and contribute to the growth of the Quality Control Department. Performs and assumes other duties and responsibilities, as may be required by the Supervisor and/or Manager, Quality Control. Supports the Winner's Circle and Blistex Quality System processes. REQUIRED EDUCATION, EXPERIENCE AND SKILLS Bachelor's degree in Chemistry, Biology, or related scientific discipline with 0-1 years of applicable laboratory experience preferable in the cosmetics/pharmaceutical OTC industry. Complies with all safety standards while on Company premises and during performance of job functions. Computer literacy in a Windows environment is required. Familiarity with Excel, Word and/or Access Database is preferred. Must possess a good understanding of the safety standards and hazards associated with a Quality Control environment. High degree of familiarity with and ability to use office machines. Must be flexible to work 1st, 2nd, 3rd shift or a modified work shift, as departmental needs demand. Willingness to accept other duties, as assigned. Must be discreet with confidential information of which he/she has access. Must possess the ability to develop and maintain an effective working relationship with internal and external customers, function as a team player, accept constructive criticism from management, and comply with Company policies. Knowledge of computerized data acquisition and analysis systems, such as Waters Empower or PE Totalchrom is required. Must possess good oral and written communication skills in Business English (spelling, grammar, and punctuation, etc.). PHYSICAL DEMANDS & ENVIRONMENT This position requires the individual to stand, walk, stoop, kneel, bend or crawl, reach with hands and arms overhead, and taste or smell 33 to 66% of the time. This position requires the individual to sit, talk or listen, and use hands to finger, handle or feel 66 to 100% of the time. This position requires the individual to climb or balance up to 33% of the time. This position will require the individual to lift up to 25 pounds 33 to 66% of the time. The vision requirements for this position includes close vision (clear vision at 20 inches or less), distance vision (clear vision of 20 feet or more), color vision (ability to identify and distinguish colors), peripheral vision (ability to see up, down, left or right while eyes are fixed on a given point), depth perception (3-dimensional vision, ability to judge distances and spatial relationships), and ability to adjust focus (ability to adjust the eye to bring an object into sharp focus). This position has exposure to wet, humid conditions (non-weather), work near moving mechanical parts or vibration, fumes, or airborne particles, and toxic or caustic chemicals up to 33% of the time. The noise level for this position will be moderate noise (Ex: Business office with typewriters and/or computer printers, light foot traffic). The Personal Protective Equipment requirements that are used in this position is a hair net, beard net, safety glasses, cut resistant gloves, and fume hood. 2nd Shift - 3:15 PM - 11:45 PM - Mon. - Fri.