Quality control analyst jobs in Waukesha, WI - 145 jobs

As the Quality Control Technician (2nd Shift), you will perform laboratory tests to determine chemical and physical characteristics or composition of in-process batches, raw materials, and finished products for such purposes as quality control, process control, or product development. You will be seated at PPG's Oak Creek, WI plant, and report to the Quality Supervisor. PPG offers excellent Medical, Dental, & Vision Benefits; matching 401k + retirement savings; and Paid Vacation, Holiday pay. Paid training is provided! Responsibilities: You will verify formula and component specifications on batch tickets. Set up, adjust, calibrate, and operate laboratory equipment and instruments such paint guns, mixers, viscometers, chemical balances, pH meters, gloss meters, solids analyzer, spectrophotometer, and other equipment. Test samples of manufactured products to verify conformity to specifications. Record test results on batch tickets and on our computer operating system. You will manage quality records and retains of production batches. Evaluate retains of production batches in response to quality complaints. Perform routine production quality checks to ensure finished products are filled and packaged according to specifications. You will perform occasional quality audits of laboratory and production work instructions to ensure compliance with our Quality Policy. Qualifications: High School Diploma or equivalent required. 1+ years of chemistry or lab testing experience. Basic knowledge of mathematics and scientific principles. Product inspection, testing and evaluation. PPG pay ranges and benefits can vary by location which allows us to compensate employees competitively in different geographic markets. PPG considers several factors in making compensation decisions including, but not limited to, skill sets, experience and training, qualifications and education, licensure and certifications, and other organizational needs. Other incentives may apply. Our employee benefits programs are designed to support the health and well-being of our employees. Any insurance coverages and benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents.

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: The Associate Production Scientist - 1st Shift at MilliporeSigma is focused on manufacturing or evaluating products according to established protocols, provides technical support to others, leads safety and quality, and performs operations in support of the group and department. Additional responsibilities include: * Shift: 1st shift Monday - Friday, 6:00am - 2:30pm * Will involve 6-12 months training necessary to learn specifics of job adequately to work independently * Safely perform operations to meet quality expectations. * Perform safe chemical-handling techniques * Ensure safety and quality throughout the process. * Adequately trained to perform tasks/assignments. * Perform routine tasks, processes and/or unit operations. * Complete the volume of work required to achieve group/departmental goals and meet deadlines. * Contribute to support functions of the department (e.g., maintain equipment, prepare reagents, restock lab supplies, perform waste disposal, design & build chemical packaging apparatus, create & maintain work instructions, troubleshoot process/equipment issues, etc.). * Communicate the status of operations and bring deviations to the attention of supervisor. * Provide complete and accurate records consistent with quality guidelines (GDP). * Ensure all applicable documentation has been filled out completely (as required by current procedures). * Interact & liaise with other departments as needed, including QC, Manufacturing, Shipping, etc. * Participate as needed in quality & safety audits. * Accurately perform procedures independently. * Comply with change control procedures. * Identify & Improve processes through application of scientific knowledge, experience, and guiding principles. * Participate in process improvements under the guidance of a Supervisor, Scientist, or your own. * Take the necessary action to resolve any unsafe conditions. * Train personnel and act as a technical consultant as needed. * Perform and interpret analytical evaluations of products and intermediates. * Supply, Interpret, & Improve information based on experience and knowledge. * Perform public speaking as needed, including monthly safety meetings. * Participation in Medical Emergency Response Team and/or Emergency Spill Response Team. Physical Attributes: * Working with highly potent / hazardous materials and chemicals safely using proper PPE * Occasional lifting and pushing of up to 50 pounds. Who You Are Minimum Qualifications * Bachelor's Degree in Chemistry, Biochemistry, Chemical Engineering, or other Life Science discipline Preferred Qualifications: * Knowledge in chemistry, math, and general science * Independent lab research experience * Strong background in chemistry, experimental design, and/or lab/manufacturing safety. * Familiar with laboratory instruments and production equipment * Knowledge of process techniques and unit operations * Familiar with analytical techniques and equipment * Good oral and written communication skills * Ability to use various computer programs, including MS Office, inventory control software (i.e., SAP), and quality management software * Basic-to-intermediate mechanical skills (i.e., use of basic hand tools) * Strong troubleshooting, organizational and interpersonal skills * Laboratory, chemical manufacturing, and/or analytical skills * Knowledge of ISO Quality standards Pay Range for this position: $27.00 - $46.00. 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!

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. Responsibilities: The Sterility Assurance Scientist is a technical role that assists in development and implementation of the site's sterility assurance programs and provides technical guidance and expertise in environmental monitoring, contamination control, aseptic process simulations, gowning/aseptic techniques, and cleaning/sanitization strategies, including disinfectant efficacy. The principal role is a position that develops and implements a technical agenda and is responsible for providing technical leadership for the Parenteral Process Team. The principal role is also expected to serve as a mentor within the TSMS team and engage in upstream and external to site activities related to sterility assurance. Key Objectives/Deliverables: (Associate/Senior) Ensure and provide oversight and technical guidance for sterility assurance programs at the manufacturing floor level. Lead or provide technical oversight for Provide technical support for activities related to sterility assurance programs including but not limited to: Airflow Pattern Testing Environmental Monitoring Performance Qualifications Aseptic Process Simulations Cleaning, Sanitization, and Disinfection Gowning within GMP Classified Areas Aseptic Processing Techniques Contamination Control Assist in the development and implementation of processes and facility monitoring to ensure effective contamination control strategies are established. (Senior) Lead or assist in the development and implementation of processes and facility monitoring to ensure effective contamination control strategies are established. (Senior) Lead/assist with support and/or provide technical expertise for developing the site's contamination control strategy and cleaning and sanitization program/strategy, and disinfectant efficacy strategies. (Senior) Lead/assist with support and/or provide technical expertise for the facility's cleanroom gowning and aseptic technique strategy/program. (Principal) Knowledge in pharmaceutical Microbiology, related to microbiological media, microbiological enumeration techniques, and microorganism isolation and identification. (Principal) Lead/provide technical oversight for one or both the Environmental Monitoring (EM) or Aseptic Process Simulation (APS) program: (EM) Authoring EM Performance Qualifications (EM PQ) and overseeing the execution. (EM) Evaluating EM data and authoring EM Trend Reports. (EM) Assist with identifying facility environmental isolates and how to create and maintain environmental isolate cultures. (APS) Authoring APS protocols and overseeing the execution. (APS) Evaluating the APS data, including personnel qualifications, and authoring APS reports. (APS) Assist with tracking and tending APS to ensure all regulatory requirements and Global Quality Standards are met for each manufacturing line/process. Apply sterility assurance risk management to evaluate manufacturing processes and associated controls with respect to potential introduction of microbial, endotoxin, and particulate contamination. Analyze microbial and manufacturing data to identify trends, process discrepancies, and opportunities for continuous improvements. Lead or provide technical support for root cause investigations associated with sterility assurance programs. Participate and/or provide technical sterility assurance support during internal and external audits. Create, execute, review, and/or approve technical documents and change controls related to sterility assurance programs. Work within cross-functional teams to implement TS/MS objective and deliver on business and quality objectives. Basic Qualifications: Bachelor's Degree in Microbiology, Biology, Biochemistry, Biochemical Engineering, Chemical Engineering, or other related scientific discipline. Additional Skills/Preferences: Demonstrated understanding and relevant experience of scientific principles required for manufacturing of parenteral drug products within operations, microbiology, environmental monitoring, sterility assurance, validation, technical services, and/or quality assurance associated cGMP pharmaceutical manufacturing. 2+ years in pharmaceutical manufacturing preferred (Microbiology, TSMS, Sterility Assurance, or related dept). Possess strong interpersonal skills to work cross-functionally within a team. Possess strong self-management and organizational skills. Possess strong oral and written communication skills for communicating to colleagues, management, and other departments. Experience with data analysis and trending. Ability to wear appropriate PPE and other safety related equipment or considerations in manufacturing, warehouse, or laboratory areas. Ability to gown into facility dedicated cleanroom attire, as required to perform job responsibilities. Additional Information: Role is Monday through Friday based and will be phased from a project support role to a routine support role as the development facility and processes progress. Must be flexible in providing support to accommodate other inputs (production schedules, shutdowns, etc.). Occasional extended hour and / or off-hour work may be required. Tasks may require repetitive motion and standing or walking for long periods of time. Travel may be required during the project phase for training and implementation of sterility assurance programs 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 $66,000 - $171,600 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

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.

Job Title: Sr. Technician, Quality Control As a **Sr. Technician, Quality Control** , you will drive product quality by executing advanced laboratory testing, analyzing results, and managing deviations to ensure compliance with internal and external standards. You will apply deep technical expertise to uphold product safety, reliability, and regulatory alignment. The Sr. Technician, Quality Control will actively contribute to departmental goals in a safety, health, environment, and quality, reinforcing customer trust and operational excellence. **Your Key Responsibilities:** - Independently perform quality control tests using various analytical and microbiological methods, ensuring accuracy and compliance with specifications. - Validate and document test results with precision and ensure timely and accurate date entry into designated systems such as log books and laboratory information management system (LIMS). - Identify, report, and process testing-related deviations in accordance with established protocols. Conduct initial laboratory investigations for validity and root cause. - Maintain responsibility for assigned laboratory instruments and maintain adequate stock of lab consumables to ensure uninterrupted operations. - Operate in full compliance with safety, health, environmental, and quality standards, meet defined performance metrics. -. Support broader performance by contributing to team goals and sharing technical insights. - Maintain a solutions-focused approach to analyze issues and troubleshoot problems both in laboratory and production environments. - Supports additional tasks, projects, and locations as required by business needs. **We Offer:** - A strong sense of accountability - you take initiative, speak up, and see things through. You are responsible and focus on what matters. - An innovator's instinct - you're always looking for better, smarter, more sustainable ways to make an impact. - Curiosity and an open mind - because you believe progress starts with asking, "Is there a better way?" - A collaborative spirit - you're at your best when working across teams, functions and countries. - A focus on unity - with stakeholders and customers. - A competitive compensation package - with comprehensive health and welfare benefits. **You Bring:** - Bachelor's degree in Biological Sciences or related fields. - 1-2 years of experience in quality control and/or laboratory. - Experience with LIMS/Sample Manager a plus. - LSS White Belt certification a plus. The hourly wage scale provided reflects the pay range dsm-firmenich expects to pay the successful candidate for the position. Individual pay offered will be based on the applicant's job-related skills, experience, relevant education, or training, and primary work location. The hourly rate is $27.00-$30.00. In addition to base salary, we also offer a comprehensive total rewards package, inclusive of annual incentive pay, a retirement savings plan, health care coverage, paid time off, recognition programs and a broad range of other benefits. All benefits and incentives are subject to eligibility requirements. **About dsm-firmenich:** At dsm-firmenich, we don't just meet expectations - we go beyond them. Join our global team powered by science, creativity, and a shared purpose: to bring progress to life. From elevating health to making fortified food and sustainable skincare, the impact of your work here will be felt by millions - every single day. Whether it's fragrance that helps you focus, alternative meat that's better for the planet, or reducing sugar without losing flavor, this is where you help shape the future of nutrition, health, and beauty for everyone, everywhere. And while you're making a difference, we'll make sure you're growing too. With learning that never stops, a culture that lifts you up and the freedom to move across businesses, teams, and borders. Your voice matters here. And your ideas? They're essential to our future. Because real progress only happens when we **go beyond, together** . **Inclusion, belonging and equal opportunity statement:** At dsm-firmenich, we believe being a force for good starts with the way we treat each other. When people feel supported, included, and free to be themselves, they do their best work - and that's exactly the kind of culture we're building. A place where opportunity is truly equal, authenticity is celebrated, and everyone has the chance to grow, contribute, and feel they belong. We're proud to be an equal opportunity employer, and we're serious about making our hiring process as fair and inclusive as possible. From inclusive language and diverse interview panels to thoughtful sourcing, we're committed to reflecting the world we serve. We welcome candidates from all backgrounds - no matter your gender, ethnicity, sexual orientation, or anything else that makes you, you. And if you have a disability or need any support through the application process, we're here to help - just let us know what you need, and we'll do everything we can to make it work. **Agency statement** : We're managing this search directly at dsm-firmenich. If you're applying as an individual, we'd love to hear from you. We're not accepting agency submissions or proposals involving fees or commissions for this role.

Job Title: Production ChemistJob Description We are seeking a dedicated and detail-oriented Production Chemist to join our team. The ideal candidate will be responsible for managing and handling all raw materials for chemical operations and ensuring the creation of new chemical compounds by operating chemical manufacturing equipment. Responsibilities * Manage and handle all raw materials for chemical operations. * Operate chemical manufacturing equipment following specific chemical formulas. * Collaborate with engineers, production personnel, and the analytical team to ensure product specifications are met. * Work with chemical engineers and R&D personnel to scale up processes. Essential Skills * Bachelor's degree in Chemistry or a related science field. * Experience in precise chemical manufacturing processes. * Proficiency in chemistry, chemical processing, and chemical synthesis. Additional Skills & Qualifications * Experience working in a laboratory setting. * Ability to work collaboratively with R&D personnel, scale-up, and process teams. Work Environment The role involves working in a chemical manufacturing environment. Initial training will be conducted from Monday through Friday during first shift hours (6 am to 2:30/3:30 pm). After three to four weeks, the position will transition to a weekend day shift, working from 6:00 pm to 6:00 am on Friday, Saturday, and Sunday. Job Type & Location This is a Contract to Hire position based out of Milwaukee, WI. Pay and Benefits The pay range for this position is $29.50 - $29.50/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Milwaukee,WI. Application Deadline This position is anticipated to close on Jan 23, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Quality Control $18-$22 ph1st shift 7am-330pm2nd shift 3pm-12am Breakdown of daily activities is generally as follows: 30% Part inspection (on manufacturing floor) 50% Assembly inspection (on manufacturing floor) 20% Processing and analysis of data Candidates should be aware that the majority of time will be spent on the manufacturing floor. Responsibilities:The position's main responsibility is inspection and documentation of parts and assemblies. Once the data is collected, it will be turned into reports that would be used to develop training and/or process improvement strategies. Secondary tasks could fill up all or part of a business day at times. These tasks could vary greatly in day-to-day activities. Examples could include discussing issues with engineers, calling vendors, updating SOP's, or addressing anything that is out of the ordinary or with which there is an issue. Requirements: Prior experience with weld and paint inspection Ability to follow directions is extremely important and then to follow through in a timely, accurate manner Strong attention to detail is extremely important Proficiency with MS Word and Excel (write reports in Word, create and use spreadsheets in Excel for analysis) Basic math skills necessary to include fractions and decimals* Strong ability in blueprint reading* Ability to read and use a tape measure* Possess mechanical ability/aptitude Prior experience using Pareto Charts preferred Prior experience in quality assurance preferred Engineering Technician experience very helpful

Urgently Hiring! 2nd Shift Quality Control Hours: 2pm-10pm (Mon-Fri) Pay: $17 Get Hired! Advance Services is hiring motivated workers to join our team with a leading plastics manufacturer in the Janesville area! We're offering competitive pay at $17 an hour, advancement opportunities, and great training. Job Duties: Read and comprehend instructions on the Quality Requirements Sheet Review and comprehend instructions on part drawings Inspect and approve existing products(visual, functional, and dimensional) Carton and pallet inspections Approve and sign-off on pallet transfers Record visual, functional, and dimensional inspections of products Complete required paperwork for red tagging non conforming materials and nonconforming finished product Perform audits and/or sorting of nonconforming finished product Setup and operate testing equipment Assist with training for new hire auditors Carry out special projects assigned Requirements: High School Diploma or GED Minimum 1-2 years of quality control/assurance experience; manufacturing environment preferred Strong computer skills (Word, Excel, Powerpoint, etc.) Ability to read and understand blueprints Excellent oral and written communication skills Strong attention to detail Data driven Self- Motivated Why work for Advance Services, Inc. Advance Services is for and about people; we are your employment specialists. Enjoy our easy application process. You NEVER pay a fee! Weekly pay. Fun Safety and attendance incentives. Health Benefits to keep you and your family healthy. Great Referral Incentives. Advance Services partners with the top companies in the area! Apply Now! #TK2 Advance Services is an equal opportunity employer

Ensures products meet all customer and company standards through the performance of line inspections, product inspections, and observation and training of Machine Operators. Essential duties and responsibilities include the following: • Examines material or product for defects. • Compares product with customer/company specifications and quality standards to ensure proper quality and completion of assembly. • Verifies specified dimensions of product. • Assures that each workstation is equipped with a specification sheet at all times. • Rejects defective parts. • Performs function test on products. • Maintains detailed system of recordkeeping. • Assists in training other employees in product specifications and configurations, safe production methods and company standards. • Observes production lines to recommend changes in working methods or conditions that would improve the product quality. Analyzes quality problem areas and develops recommended solutions. • Reads actual cycle times of injection molding machines. • Maintains clean work area. Qualifications: Required Education and Experience: • High School diploma or equivalent • 6 - 12 months of production work experience Knowledge of: • Basic math • Knowledge of simple measurement Ability to: • Ability to perform oral and written communication 2nd shift Monday - Friday 2:30pm - 11:00pm $17.40 an hour incentive of a $25.00 bonus first 80 hours worked with perfect attendance incentive .25 cent increase once worked 30 days with perfect attendance EOE

We are seeking an experienced, detail-oriented Quality Control Chemist to add to our 2nd-shift team. The ideal candidate has a strong background in chemistry and thrives in a fast-paced and team-oriented laboratory environment. QC Chemist Hours: Approximately 2p - 1a, Monday - Thursday, some occasional work outside of normal schedule may be required. Reports to: Quality Manager Summary: The QC Chemist will support the manufacturing process by performing laboratory analysis of raw materials, intermediate blends, and finished goods. The QC Chemist will have strong complex instrumentation knowledge and support calibration and maintenance of lab instruments, as well as assisting in the transfer of customer test methods as necessary. Responsibilities: · Follow standard operating procedures and quality directives as outline by the IKI Quality Manual. · Perform raw material, intermediate blend, and finished product testing to ensure quality on all manufactured goods. · Prioritize workload and schedule testing to align with production and distribution plans. · Support the transfer of customer test methods, as needed. · Assist in the development and review of standard operating procedures for laboratory equipment, instruments, and processes. · Complete the required preventative maintenance on lab instruments and equipment, as necessary. · Document all test results in written and electronic format where appropriate. · Assist in the training of other lab personnel on laboratory instruments and new test methods. · Perform other duties as assigned. Required Skills & Abilities: · Attention to detail and thoroughness. · Ability to thrive in a fast-paced environment. · Maintain clean and organized workspace. · Effective prioritization and self-motivation skills. · Ability to read, interpret, and correlate data. · Excellent math skills and familiarity with MS Office suite, especially Excel. · Ability to communicate effectively cross-functionally. Education & Experience: · B.S. in chemistry, or similar discipline, required. · Minimum of 3 years of lab experience required. · Experience with HPLC, GC, pH, UV-vis, FTIR, Karl Fisher, and other wet chemistry techniques required. · Experience with HPLC, GC, and general analytical test method development and transfer highly preferred. · Experience with microbial testing and/or procedures is highly preferred. · Experience with contract manufacturing and testing preferred. Work Environment: Laboratory environment with exposure to chemicals. Proper PPE must be worn, and safety precautions must be followed. Physical Demands: Stands 75%, sits 25%, occasional lifting up to 50 lbs.

We are seeking an experienced, detail-oriented Quality Control Chemist to add to our 2nd-shift team. The ideal candidate has a strong background in chemistry and thrives in a fast-paced and team-oriented laboratory environment. QC Chemist Hours: Approximately 2p - 1a, Monday - Thursday, some occasional work outside of normal schedule may be required. Reports to: Quality Manager Summary: The QC Chemist will support the manufacturing process by performing laboratory analysis of raw materials, intermediate blends, and finished goods. The QC Chemist will have strong complex instrumentation knowledge and support calibration and maintenance of lab instruments, as well as assisting in the transfer of customer test methods as necessary. Responsibilities: · Follow standard operating procedures and quality directives as outline by the IKI Quality Manual. · Perform raw material, intermediate blend, and finished product testing to ensure quality on all manufactured goods. · Prioritize workload and schedule testing to align with production and distribution plans. · Support the transfer of customer test methods, as needed. · Assist in the development and review of standard operating procedures for laboratory equipment, instruments, and processes. · Complete the required preventative maintenance on lab instruments and equipment, as necessary. · Document all test results in written and electronic format where appropriate. · Assist in the training of other lab personnel on laboratory instruments and new test methods. · Perform other duties as assigned. Required Skills & Abilities: · Attention to detail and thoroughness. · Ability to thrive in a fast-paced environment. · Maintain clean and organized workspace. · Effective prioritization and self-motivation skills. · Ability to read, interpret, and correlate data. · Excellent math skills and familiarity with MS Office suite, especially Excel. · Ability to communicate effectively cross-functionally. Education & Experience: · B.S. in chemistry, or similar discipline, required. · Minimum of 3 years of lab experience required. · Experience with HPLC, GC, pH, UV-vis, FTIR, Karl Fisher, and other wet chemistry techniques required. · Experience with HPLC, GC, and general analytical test method development and transfer highly preferred. · Experience with microbial testing and/or procedures is highly preferred. · Experience with contract manufacturing and testing preferred. Work Environment: Laboratory environment with exposure to chemicals. Proper PPE must be worn, and safety precautions must be followed. Physical Demands: Stands 75%, sits 25%, occasional lifting up to 50 lbs.

Web Applicant Quality Control We are looking for experienced QA candidates in food manufacturing for Kenosha Resume and in-person interview required The QA Technician is responsible of ensuring that the manufacturing process is carried in a food safe and wholesome manner. The QA Technician is also responsible for identifying and resolving quality issues, working hand in hand with operations and checking that all products are manufactured according to the correct product specification and flow. The QA Technician needs to be familiar with HACCP and GMP. The QA Technicians reports to the SQF Practitioner. Required Skills: Bilingual - Can read/write in English Quality experience in a fresh food manufacturing environment Food Safety Skills: Recommended to have GMP's, HACCP, CCP experience. Experience with internal quality inspections and audits Maintain a positive work environment Must be willing to work designated shifts Note: Flexibility with schedule and available to work overtime when needed. Able to work in the cold Essential Duties and Responsibilities: Work standing or walking in cold environment (below 40 °F) for most working shifts. Perform very physical duties, including but not limited to pushing, pulling, lifting, twisting, and walking. Provide independent oversight of processes, verifying compliance to company standards and policies Maintain a clear understanding of Quality Assurance Programs and SOPs. Adhere to all regulatory rules and regulations, ensuring that Food Safety and product performance standards are met. Monitor HACCP critical control points Enforce GMPs Calibrate and maintain equipment Responsible for placing equipment and product on hold. Verify the concentrations of the chemicals and sanitizers. Perform daily Pre-operational inspections and Pre-op ATP testing. Conduct product and process testing. Monitor and assure compliance of allergen management, Organic processing, and USDA standards. Develop and maintain operational quality standards, traceability, batch sheets and specification sheets. Use all safety equipment and PPE the company provides according to instructions. Steel-toe shoe or boot/non-slip required for everyone in all departments. Shift: to be discussed in interview. Flexibility with schedule required 1st shift 7:00-3:30 2nd shift 2:00-Finish *** Everyone gets Sunday off and 1 random weekday off*** Call or text for more information ************ Labor Solutions LLC. Is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender, identity, national origin, veteran or disability status 18.00 Qualifications Quality in food production

As a Quality Control Technician (3rd Shift) you will perform laboratory tests to determine chemical and physical characteristics or composition of in-process batches, raw materials, and finished products for such purposes as quality control, process control, or product development. You will be seated at PPG's Oak Creek, WI plant, and report to the Quality Supervisor. PPG offers excellent Medical, Dental, & Vision Benefits; matching 401k + retirement savings; and Paid Vacation, Holiday pay. Paid training is provided! Responsibilities: You will verify formula and component specifications on batch tickets. Set up, adjust, calibrate, and operate laboratory equipment and instrument such paint guns, mixers, viscometers, chemical balances, pH meters, gloss meters, solids analyzer, spectrophotometer, and other equipment. Test samples of manufactured products to verify conformity to specifications. Record test results on batch tickets and in our computer operating system. You will manage quality records and retains of production batches. Evaluate retains of production batches in response to quality complaints. Perform routine production quality checks to ensure finished products are filled and packaged according to specifications. You will perform occasional quality audits of laboratory and production work instructions to ensure compliance to our Quality Policy. Qualifications: High School Diploma or equivalent required. 1+ years of chemistry or lab testing experience. Basic knowledge of mathematics and scientific principles. Product inspection, testing and evaluation. PPG pay ranges and benefits can vary by location which allows us to compensate employees competitively in different geographic markets. PPG considers several factors in making compensation decisions including, but not limited to, skill sets, experience and training, qualifications and education, licensure and certifications, and other organizational needs. Other incentives may apply. Our employee benefits programs are designed to support the health and well-being of our employees. Any insurance coverages and benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents.

Job Title: Production ChemistJob Description We are seeking a skilled Production Chemist to join our team and contribute to our chemical manufacturing processes. You will be responsible for handling raw materials, operating manufacturing equipment, and ensuring that all chemical operations are performed according to specific formulas to create new chemical compounds. Responsibilities * Handle and manage all raw materials for chemical operations. * Operate chemical manufacturing equipment and follow specific chemical formulas. * Collaborate with engineers, production personnel, and the analytical team to ensure product specifications are met. * Work closely with chemical engineers and R&D personnel to scale up processes. Essential Skills * Bachelor's degree in Chemistry or related scientific field. * Experience in chemical processing and manufacturing. * Ability to work with R&D personnel, scale-up and process teams, operations, and laboratory settings. Additional Skills & Qualifications * Experience in chemical synthesis. * Strong laboratory skills. Work Environment The role involves working in a chemical manufacturing setting. Initial training occurs Monday through Friday on first shift hours (6 am to 2:30/3:30 pm). After training, the schedule shifts to a weekend day shift from 6:00 am to 6:00 pm on Friday, Saturday, and Sunday. Job Type & Location This is a Contract to Hire position based out of Milwaukee, WI. Pay and Benefits The pay range for this position is $29.50 - $29.50/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Milwaukee,WI. Application Deadline This position is anticipated to close on Jan 21, 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 for other accommodation options.

Quality Control Inspector - 1st Shift, 7am-3:30pmPay: $20-$24/hour (Based on Experience) At our client, they don't just build components-they ensure quality at every step. As a Quality Control Inspector, you'll play a critical role in maintaining the excellence our customers depend on. If you're detail-driven, reliable, and ready to grow within a fast-paced manufacturing environment, this is your opportunity to make an impact. We are seeking a meticulous and motivated Quality Control Inspector for our 1st shift team. You will be responsible for performing Incoming, In-Process, and Final Inspections, using traditional metrology tools to ensure components meet required specifications and quality standards. Essential Duties and Responsibilities: Inspect alignment and dimensions of parts using ID/OD micrometers, height stands, and calipers Perform manual drafting to document dimensional requirements Verify parts against product specifications, drawings, and part lists Visually examine parts and document production results Ensure all inspections and records comply with the Quality Management System and Customer Requirements Confirm assembly completeness and identify missing or incorrect hardware Participate in ongoing training and maintain equipment certifications Required Competencies & Skills: Proficient with manual inspection tools (Micrometers, Calipers, Height Stands) Ability to read and interpret manufacturing drawings and blueprints Strong verbal and written communication skills Solid mathematical knowledge including geometry, trigonometry, fractions, decimals, and layout functions Excellent critical thinking, problem-solving, and time management abilities Adaptable and able to work both independently and as part of a team Preferred Qualifications: Valid driver's license Prior experience in a manufacturing or quality control environment Exceptional attendance record (required) Completion of Overhead Crane and Forklift Training (training provided upon hire if needed) Physical Requirements: Frequent standing, walking, climbing, stooping, kneeling, bending, and lifting (up to 50 lbs) Frequent use of hands, tools, and inspection equipment Occasional talking or hearing in a production setting

Job Title: Senior Quality Control Technician Reporting to the General Manager, the Senior Quality Control (QC) Technician serves as a pivotal leader within our contract job shop environment, specializing in sheet metal fabrication. This senior role is responsible not only for meticulous inspection and documentation-including oversight of PPAP (Production Part Approval Process) and ISIR (Initial Sample Inspection Report) requirements-but also for driving a culture of continuous improvement across quality systems and production processes. In addition to performing all core QC duties, the Senior QC Technician is expected to be a proactive change agent, advocating for process enhancements and inspiring team members to speak up and initiate positive change. This role encourages open communication and collaboration to identify inefficiencies, recommend actionable improvements, and champion the adoption of best practices throughout the organization. Key Responsibilities • Lead and perform the preparation, review, and submission of PPAP and ISIR documentation for contract sheet metal jobs, ensuring all deliverables exceed customer and regulatory requirements • Audit welds and fabricated parts, validating adherence to specifications, tolerances, and quality standards • Mentor and train junior QC personnel, fostering a team oriented toward continuous learning and process excellence • Champion continuous improvement initiatives by identifying opportunities for process optimization and cost savings • Act as a change agent-proactively propose, communicate, and help implement new or improved quality procedures; encourage others to voice insights, observations, and concerns to enhance workflow and product quality • Lead root cause analysis and corrective action processes, especially as they relate to PPAP/ISIR non-conformances or customer feedback • Represent QC in cross-functional teams, bringing a solutions-oriented approach to meetings with production, engineering, and management • Support customer and third-party audits, ensuring all quality documentation, including PFMEA, Control Plans, and Process Flow Diagrams, is accurate and up to date • Maintain and improve systems for documentation, traceability, and reporting in compliance with ISO standards and specific contract customer requirements Required Skills and Experience • High school diploma or GED equivalent required; technical degree or relevant certifications in quality/manufacturing preferred • Minimum 5 years' experience in an ISO-certified contract job shop, with advanced expertise in sheet metal fabrication and quality systems • Extensive working knowledge of PPAP and ISIR processes, including documentation, review, and direct interaction with contract customers • Proficiency with advanced inspection tools (calipers, micrometers, CMMs), and a strong command of GD&T and blueprint interpretation • Demonstrated experience in leading quality improvement programs and successfully implementing process changes Physical Demands • Performing physical activities that require considerable use of your arms, hands, fingers, legs and moving your whole body, such as lifting, balancing, walking, stooping, handling of materials, and operating machinery • Perform repetitive motions using your hands and fingers such as, but not limited to, grasping, gripping, and holding • Carrying & lifting up to 50lbs. frequently • Specific vision abilities required by this job include close vision, distance vision, color vision, depth perception, and the ability to adjust focus Shift: Mon-Thur 5am -3:30pm We are an equal opportunity employer

As a Development Chemist - Liquid Industrial, you will be responsible for customer-facing development opportunities in basecoats and clear coats for the Industrial Coatings Liquid OEM segment. You will work closely with the Associate Manager, S&T and sales managers in support of key customers while thoughtfully applying formulation expertise in a high-energy environment that encourages your growth! You will play a key role in formula design, product preparation and application, and the testing of coatings to meet challenging customer requirements. This is an onsite role in our Oak Creek, WI. facility. Key Responsibilities Follow all PPG EH&S and safety guidelines 100% of the time while working. Lead projects and directly oversee work of contractors and technicians. Prepare and apply liquid coating products for testing against customer defined specifications and requirements. With feedback from technical service, address customer complaints/concerns through root cause analysis and/or formulation changes. Communicate and ensure recordkeeping through written/verbal summaries, reports, and presentations to both internal and external customers. Act as a liaison to manufacturing by answering QC questions, working to maintain formula alignment, addressing problem formulas, and product quality concerns through experimental work. Positively motivate peers and associates in cooperative efforts 100% of the time while working on the team. With direction from the customer, formulate and test new ideas directed at improving coatings properties to add value through improved performance. Follow and maintain product formulation guidelines. The chemist will also be responsible for identifying new or alternative formulation tools that can be incorporated into the main product platform through extensive testing and validation. Able to handle multiple projects in a high-pressure environment with a demanding customer. Communicate updates as well as any issues, roadblocks, questions, or concerns quickly and effectively within the team environment so that solutions can be implemented as soon as possible. Stay up to date on new raw material product launches and material literature through engagement with suppliers. Network internally within PPG to build relationships and seek cross functional solutions to complex problems. Serve as a resource to troubleshoot issues both within the direct team and as part of the larger group supporting other chemists. Qualifications Bachelor's Degree in a Chemistry, Polymer Science, Coatings Science, or Chemical Engineering or global equivalent in related discipline. Master's degree, PhD, or global equivalent a plus. 5+ years of coatings formulation experience and proven laboratory experience. Only U.S. Citizens, Green Card holders, and political asylees or refugees are eligible to apply PPG pay ranges and benefits can vary by location which allows us to compensate employees competitively in different geographic markets. PPG considers several factors in making compensation decisions including, but not limited to, skill sets, experience and training, qualifications and education, licensure and certifications, and other organizational needs. Other incentives may apply. Our employee benefits programs are designed to support the health and well-being of our employees. Any insurance coverages and benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents.

Job Title: Production ChemistJob Description We are seeking a skilled Production Chemist to join our team and contribute to the creation of high-purity chemical compounds. This role involves working closely with our R&D personnel, scale-up and process teams, operations, and laboratory staff to ensure the precise manufacture of chemical products for a specialized customer base. Responsibilities * Manage and handle all raw materials for chemical operations. * Operate chemical manufacturing equipment and follow specific chemical formulas to create new chemical compounds. * Collaborate with engineers, production personnel, and the analytical team to ensure product specifications are met. * Work with chemical engineers and R&D personnel to scale up processes. Essential Skills * Advanced education in the sciences, such as a Bachelor's degree in Chemistry. * Experience in chemical operations and processing. * Proficiency in chemistry and chemical synthesis. Additional Skills & Qualifications * Experience working in a laboratory setting. * Knowledge of chemical engineering and manufacturing processes. Work Environment The work environment includes training from Monday to Friday on first shift hours (6 am to 2:30/3:30 pm). After three to four weeks, the schedule transitions to a weekend day shift from 6:00 am to 6:00 pm on Friday, Saturday, and Sunday. The role requires working in a chemical manufacturing setting. Job Type & Location This is a Contract to Hire position based out of Milwaukee, WI. Pay and Benefits The pay range for this position is $29.50 - $29.50/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Milwaukee,WI. Application Deadline This position is anticipated to close on Jan 26, 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 for other accommodation options.

Do you have an eagle eye for detail and a passion for ensuring top-notch product quality? We're looking for a diligent Quality Control Inspector to join our dynamic team!Daily Activities Breakdown: 30%: Part inspection (on manufacturing floor). 50%: Assembly inspection (on manufacturing floor). 20%: Processing and analysis of data. Responsibilities: As our Quality Control Inspector, you'll play a crucial role in inspecting parts and assemblies, ensuring they meet our exacting standards. Your keen eye and meticulous documentation skills will help us drive continuous improvement in our processes. From analyzing data to collaborating with engineers, your contributions will be integral to our success.Requirements: Experience with weld and paint inspection preferred. Strong attention to detail and ability to follow directions. Proficiency in MS Word and Excel for report writing and data analysis. Basic math skills and ability to read blueprints. Mechanical aptitude and prior quality assurance experience are pluses. Engineering Technician experience is advantageous. Why Join Us? Exciting opportunity to be part of a dynamic team committed to excellence. Competitive compensation and opportunities for growth. Collaborative work environment where your contributions are valued. Make a difference by ensuring top-quality products reach our customer