Quality control analyst jobs in Wisconsin - 473 jobs

ESSENTIAL JOB FUNCTIONS: Rust-Oleum Corporation is a worldwide leader in protective paints and coatings for both home and industry. We offer a wide product range including decorative fashion paints, durable industrial roof repair coatings and, of course, the famous rust-fighting formula that started it all. The primary result expected from the Quality Control Technician will be to assure product quality by preparing samples, conducting quality control inspection and testing of components, dispersions, and finished goods, determining adjustments for batches that do not conform to requirements, documenting inspections, and insuring calibration of testing equipment. Tasks PROFILE: Typical tasks for this position include (but are not limited to) the following: Perform testing of production batches, incoming raw materials, finished goods, and components to determine conformance to specifications. Judge as “fit for release” production batches, incoming raw materials, finished goods, and components that are in conformance to all specifications and visually acceptable. Determine and communicate batch adjustments for any batches that do not conform to requirements, utilizing batch history, adjustment guidelines, and consultation with the Senior QC Technician, Assistant Supervisor, or QC Manager. Perform validation testing during filling to insure integrity of finished goods, including labeling, packaging, and fill weights. Communicate current status of inspections to Senior Technicians, Assistant Supervisor, or QC Manager. Communicate issues with work instructions and procedures to Senior Technicians, Assistant Supervisor, or QC Manager. Document inspection results. Responsibilities/Expectations: Communicate with Supervisors, peers, or subordinates: provide information to supervisors and co-workers in written form or in person. Maintain a good record of attendance and punctuality. Learn all manual tasks performed within the department. Perform tasks assigned using specific operating procedures, and following department specific quality control processes and procedures. Treat people with dignity and respect. Conduct all business with integrity. Adhere to Rust-Oleum Corporation Quality principles and participate in all departmental and company-wide Quality activities. Follow all safety procedures and company policies. QUALIFICATIONS: KNOWLEDGE English Language - Knowledge of the structure and content of the English language including the meaning and spelling of words, rules of composition, and grammar. Production and Processing - Knowledge of raw materials, production processes, quality control, costs, and other techniques for maximizing the effective manufacture and distribution of goods. Skills Quality Control Analysis - Conducting tests and inspections of products, services, or processes to evaluate quality or performance. Reading Comprehension - Understanding written sentences and paragraphs in work related documents. Critical Thinking - Using logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions or approaches to problems. Science - Using scientific rules and methods to solve problems. Active Listening - Giving full attention to what other people are saying, taking time to understand the points being made, asking questions as appropriate, and not interrupting at inappropriate times. Active Learning - Understanding the implications of new information for both current and future problem-solving and decision-making. Speaking - Talking to others to convey information effectively. Writing - Communicating effectively in writing as appropriate for the needs of the audience. Operation Monitoring - Watching gauges, dials, or other indicators to make sure a machine is working properly. Shift: 6pm-6:15am; 2-2-3 shift rotation continuous operations schedule. Rust-Oleum is an equal opportunity employer. Employment selection and related decisions are made without regard to sex, race, age, disability, religion, national origin, color, or any other protected class.

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- Weekend Night Shift in Madison, WI is primarily focused on safe and efficient manufacturing of active pharmaceutical ingredients (API's) according to current Good Manufacturing Practice (cGMP) requirements. This role is lab-based and primarily focused on executing required production operations to support the end users and patients of the compounds produced at MilliporeSigma. These responsibilities include but are not limited to executing existing production procedures, updating supporting documents, and maintaining the safety and quality of the manufacturing environment. Additional responsibilities include: * D Shift: Rotating shift, Thursday - Sunday 6:30pm - 7:00am, then Friday - Sunday 6:30pm - 7:00am * Demonstrating proper lab safety practices, and work in accordance with FDA, OSHA, EPA, DNR, DOT, and other regulatory agency guidelines. * Functioning as a Primary Operator for a single group of GMP Production areas (i.e. Kilo Labs). Draft preliminary reports detailing deviations from written procedures and potential contributing factors. * Utilize and provide minor updates to a variety of written procedures, including operating procedures with assistance from a supervisor or SME. * Help to identify and immediately correct equipment, process, and safety issues in the lab. Mentor new employees by performing supplemental technical and on the job training. Participate in a team-based, multi-shift manufacturing environment by actively engaging in inter-shift communication and maintaining high quality in-lab housekeeping. * Take independent ownership over a departmental support responsibility. * Engage in personal and professional career development through active participation in development objectives. * Provide departmental support through additional tasks as directed by department leadership. Physical Attributes: * Working with highly potent / hazardous materials * Standing for long periods of time * Lifting and moving up to 50 pounds with the assistance of equipment or teammates * Utilizing proper personal protective equipment which could include but is not limited to; respiratory protection such as dust masks, half/full face respirators, supplied air, etc., and full body protection such as disposable coveralls, hazmat suits, etc., MilliporeSigma issued work uniforms and Lab Coats Who You Are: Minimum Qualifications: * Bachelor's Degree in Chemistry, Biochemistry, Chemical Engineering, or other Life Science discipline Preferred Qualifications: * Ability to read and understand written protocols. * Strong computer literacy (Microsoft Office and Outlook tools, Electronic Document Management Systems, etc.) * Effective oral and written communication skills * Mechanical and technical aptitude * Able to operate hand tools, calculators, and weighing / measuring devices * Strong mathematical skills * Possess a high degree of internal motivation * Ability to multi-task while paying close attention to detail Pay Range for this position: $27.00-$53.00 per hour The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. RSREMD RSRERSREMDMD RSREMD 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

Elephas, a Madison, WI-based biotechnology start-up company, is seeking a highly motivated Scientist to support Manufacturing (MFG), Quality Control (QC), and equipment oversight within our Operations team. This individual will assist in MFG and QC of reagents and consumables utilized with our Elephas platform. This individual will support equipment preventative maintenance (PM) and calibrations (CAL) ensuring documentation is maintained in the computerized maintenance management system (CMMS). The individual will work closely with the lead scientists, technical transfer team, R&D, Quality, and Operations to ensure successful production and release of products into inventory and management of all equipment onsite. This role will utilize appropriate inhouse systems and tools to execute the production runs based on sales and operating plans (S&OP) and will work closely with outside vendors to complete all PMs and CALs where needed. This candidate will be self-motivated to learn, and comfortable in a fast-paced and highly collaborative environment. Essential Duties and Responsibilities Assist in labeling, manufacturing, dispensing, and quality control of Elephas products Partner with lead scientists and technical transfer team to execute manufacturing, analytical testing methods, and quality control assays for production and release of the products to inventory Support scaling activities for manufacture of reagents, consumables, and testing methods Follow protocols, procedures, and work instructions to support manufacturing and quality control capabilities in compliance with RUO, GMPs, FDA 21 CFR 820, and ISO13485 guidelines Draft and review Standard Operating Procedures (SOPs) and related manufacturing process documentation as required aligned with the Quality Management System (QMS) Assist in troubleshooting production and quality control related performance issues and out of specifications working closely with senior scientists to identify root cause and develop process improvements to reduce and mitigate risk Support CAPAs, non-conformances, deviations, and investigations with Quality partners and Operations leaders to drive action and mitigations going forward Follow proper lab processes and documentation including equipment use and safety practices Comfortable working with biological and chemical materials, and instrumentation Execute PMs and CALs as required working with outside vendors or internal employees to ensure proper documentation and completion of records and tracking in the CMMS Support onboarding of new equipment assets into lab spaces Education/Experience/Skills Bachelor's degree in Life Sciences field or related discipline Computer proficiency of Microsoft Office Suite Strong attention to detail Ability to problem solve with good analytical skills Excellent verbal and written communication skills We offer our employees competitive compensation and benefits, including paid time off, health insurance, life insurance, flexible spending accounts, a 401(k) plan, and stock options. DISCLAIMER The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job. We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class.

Full-time Description The Quality Control Technician I plays a key role in maintaining American Phoenix, Inc.'s reputation for excellence in rubber manufacturing. This position is responsible for performing precise tests on rubber compounds using specialized laboratory equipment to ensure product integrity and compliance with customer specifications. Accuracy and attention to detail are critical to maintaining our quality standards. This position reports to our Quality Manager. Summary of Duties and Responsibilities Follow all company and laboratory safety procedures at all times. Maintain a neat, organized, and clean work area. Perform testing of rubber compounds in accordance with customer and internal specifications. Analyze and interpret test data to assist in determining material release status. Prepare rubber samples as needed (cutting, milling, curing, and stamping). Troubleshoot issues such as test failures, retesting, or data discrepancies. Enter test results accurately into data systems and complete customer data packets. Tag and release finished goods after testing and approval. Shift Information This is a full-time, 8-hour afternoon shift position: Monday - Friday, 3:00 PM to 11:00 PM Probationary and Training Period All new Quality Control Technician I employees will undergo a 90-day probationary period. During this time, employees are expected to demonstrate proficiency in the required laboratory testing procedures and safety practices. Successful completion of this period, including supervisor sign-off, is required to continue employment in this position. This 90-day period may be adjusted by management depending on business demands, employee leave, or other applicable factors. If management does not observe satisfactory progress or improvement within this period, proper communication and feedback will be provided to the employee to support development and clarify expectations. Our Benefits Include: Health Insurance Dental Insurance 401(K) with Company Match Company paid Short-term and Long-term Disability Company paid Life Insurance 9 Paid Holidays Employee Assistance Program Immediate PTO Accrual 2 Personal Days Annually Optional Paid Shower Time at the End of Each Shift Requirements Required: High school diploma or equivalent. Preferred: Working knowledge of Microsoft Excel and other Windows-based software. Previous laboratory experience or familiarity with material testing environments. Skills, Knowledge, and AbilitiesCandidates should demonstrate the following: Strong safety awareness. Exceptional attention to detail, accuracy, and precision. Ability to learn and follow laboratory procedures. Effective communication and teamwork skills.

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.

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.

Laboratory Analyst 1 Imagine your future with us At ALS, we encourage you to dream big. When you join ALS, you join a purpose and values-driven team that empowers you to innovate, create, and thrive. Our global team turns up each day with passion and commitment to do amazing things, always challenging our thinking to find ways to solve some of the world's most complex problems for a safer, healthier world. Responsibilities About the role ALS Food Safety provides an extensive range of food analytical testing services, including food production environments and raw and cooked meat, dairy, produce, seafood, and animal feeds. We work closely with our clients to ensure their needs are met now and in the future. Due to growth, ALS is currently recruiting for Laboratory Analysts in our Marshfield, WI Food Lab. We will train the right candidates! Entry Level Laboratory Analysts perform basic laboratory tests. Analysts receive, log, and prepare samples and perform analysis according to procedures and test methods. Duties include: Perform calculations as required when conducting analytical preparations. Calibrate equipment as required. Maintains an understanding of and ensures compliance to Quality System including the manual, system procedures (QMSPs). Perform housekeeping duties as required. About you High school diploma or equivalent Good communication and collaboration skills (Teamwork!) Multi-tasked, organized, and detail oriented. Problem solving capabilities. Previous experience working in another laboratory on in the food safety sector. Life Science degree a plus! Working conditions 4/10 work schedule. Position requires significant time working in a laboratory environment between ten to twelve (10-12) hours per business day. Must be able to stand, bend, push, pull, stoop and crouch up to 80% of the time while performing the duties of this position. Must be able to lift (with both hands) and/or move up to 50 pounds and occasionally lift and/or move heavier loads with assistance. Qualifications Working at ALS Our people are our most valuable asset and drive our success at ALS. We are a diverse community of dedicated professionals united by our passion to make a difference in the world. We reward excellence and uphold our values in our work and how we treat each other. At ALS, you'll be supported to expand your skills and develop new ones so you can reach your full potential. We invest in our people with a range of programs and provide opportunities across the company, giving our people scope to grow diverse careers and develop as leaders. We want everyone to have a safe, flexible and rewarding career that makes a positive impact on our people, the planet and the communities where we work. Our benefits include: Structured wage increases Food Safety Incentive program Comprehensive benefit package including medical, dental, and vision coverage, life and disability insurance, retirement plan with company match, employee assistance and wellness programs, access to company perks) Additional vacation days for years of service Business support for education or training after 9 months with the company Learning & development opportunities (unlimited access to e-learnings and more) About ALS ALS is a global leader in scientific testing, providing comprehensive testing solutions to clients in more than 60 countries across a wide range of industries, including environment, food and beverage, mining, personal care, pharmaceutical, healthcare and equipment reliability. Using state-of-the-art technologies and innovative methodologies, our dedicated international teams deliver the highest-quality testing services and personalized solutions supported by local expertise. We help our clients leverage the power of data-driven insights for a safer and healthier world. Everyone matters ALS is proud to be an equal opportunity employer committed to achieving and maintaining a workforce which reflects and affirms the diversity of our society ALS is a VEVRAA Federal Contractor. EOE AA Minority, Female, Veteran, Individuals with Disabilities. Click Here to view the EEO is the Law poster Click Here to view the FMLA Law poster Click Here to view the EPPA Law Poster Click Here to view the Pay Transparency Provision Click Here to view company E-Verify Participation Poster ALS also welcomes applications from people with all levels of ability. Accommodation is available on request for candidates taking part in all aspects of the selection process.

Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. The Position The Quality Control Intern will support quality operations at Arrowhead Pharmaceuticals by assisting with raw materials supplier qualification and analytical method verification activities. This internship offers hands-on experience in a GMP laboratory environment while contributing to critical quality processes that support manufacturing timelines. The intern will work alongside QC analysts to execute testing, documentation, and verification activities that ensure raw materials meet quality and regulatory standards. This is an 11-week Summer Internship Program paying $21.00 per hour and requires full-time, onsite work five days per week at the designated location. Responsibilities Read and understand the QC training program, procedures, and associated documentation. Observe and shadow trainers during QC laboratory procedures, including analytical techniques and instrumentation. Perform and execute QC procedures and documentation as instructed by trained QC personnel. Evaluate the training program to identify gaps, unclear steps, or opportunities for improvement. Assess training effectiveness across multiple QC techniques to develop a comprehensive understanding of QC processes. Compile findings into a detailed report with recommendations for potential updates and improvements to the training program. Follow all GMP, safety, and quality requirements while working in the laboratory Requirements Currently enrolled student at an accredited university or college, with a minimum of two years completed toward a degree in Chemistry, Biochemistry, or a related scientific discipline. Understanding of laboratory environments and interest in analytical testing and method verification. Interest in learning and applying a variety of laboratory instrumentation and techniques. Excellent verbal and written communication skills, including comfort presenting in group settings. Strong problem-solving and organizational skills. Proficiency in Microsoft Office applications. Preferred Prior experience in a QC, analytical, or laboratory setting. Familiarity with QC procedures, instrumentation, or analytical methods. Interest in quality systems, training programs, or continuous improvement. Motivation to pursue a career in Quality Control or Pharmaceutical Sciences. Comfort working in a regulated GMP environment. Wisconsin pay range $9,240-$9,240 USD Arrowhead provides competitive salaries and an excellent benefit package. All applicants must have authorization to work in the US for a company. California Applicant Privacy Policy

Selene Holdings is a multiple-lines business financial services firm with a mortgage servicing company, a loan diligence company, a title company, an insurance brokerage, and a real estate owned company. We have office locations in Dallas, TX, Jacksonville, FL, and Salt Lake City, UT. Founded in 2007 to address needs in the mortgage industry, Selene strives to provide amazing client and borrower experiences. A positive attitude coupled with proven creative thinking and actions are all attributes we seek in every one of our employees. If you want to make a difference, then Selene is the place for you! Position Summary: Diligence Quality Control II (Part-Time) is focused on controlling a high quality product, enhancing loan review processes and developing specialist expertise for long term career growth. Essential Duties and Responsibilities include the following. Other duties may be assigned. Responsible for the Quality Control examination of loan reviews completed by Loan Review Analysts. Provide real time loan kick back feedback to Loan Review Analysts pertaining to errors and determining corrective actions. Ensure regulatory compliance for loans reviewed. Escalate error trends to management. Develop deep understanding of specific client guidelines. Handle escalated and countered client conditions with minimal guidance. Assists with loan review system testing and enhancement. Ongoing development of subject matter expertise - aim to become go to subject matter expert for various specialist loan review QC topics. Assist with problem solving, issue resolution and loan review guidance. Assist in providing guidance on daily matters, such as, questions regarding Underwriting Guidelines or Compliance questions relating to TRID, Reg X, TILA or others to LRAs. Maintains high level of confidentiality to protect privacy rights. Adheres to internal controls to reduce errors and customer complaints. Responsive to internal and external customers' needs in a timely, accurate and professional manner. 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. The qualified candidate must have: Maintains a current knowledge of underwriting guidelines, investor guidelines, regulatory compliance and TRID practices. Minimum 3-5 years mortgage underwriting and mortgage quality control within the origination or due diligence space. Strong understanding of condition clearing processes and their impact on loan grades. Basic understanding of the credit rating agency requirements. Knowledge of USPAP standards, supplemental valuation products and reconciliation. Ability to produce underwriting reports, analyze results, identify issues and take corrective actions. Experienced with reading, analyzing and understanding various loan servicer pay histories and servicing documentation. Developing leadership skills with the ability and experience to manage people. Effectiveness as a team player. Ability to easily prioritize job duties according to the needs of the company. Strong sense of professionalism and positivity. Excellent oral and written communication skills. Ability to develop rapport with all levels of associates and establish credibility. Excellent listening skills and the ability to use good judgment. Strong interpersonal/relationship building skills. Problem solving and decision making ability. Ability to produce quality work. Ability to think and solve problems strategically. Strong analytical and organizational skills. Excellent attention to detail. Ability to multi-task and consistently meet multiple deadlines. Education/Experience: Minimum 3-5 years' experience with emphasis on non-agency underwriting and QC desired. Experience in second level reviews; escalations and performance management required. Bachelor's degree preferred. Computer Skills: Working knowledge of and experience with Microsoft Office (Word, Excel, and Outlook). Previous experience with mortgage due diligence software, Andor, MSP, Black Knight/LPS and Fiserv preferred. Why Selene? Benefits Selene Finance LP is committed to the total wellbeing of its employees and therefore offers one of the best benefits packages available in the industry today, which includes: Paid Time Off (PTO) Medical, Dental &Vision Employee Assistance Program Flexible Spending Account Health Savings Account Paid Holidays Company paid Life Insurance Matching 401(k) Plan The job requirements listed above are representative of the knowledge, skills, and/or abilities required. This job description is not an inclusive list of all duties and responsibilities of this position. Incumbents will be required to follow any other job-related instructions and to perform any other job-related duties requested by any person authorized to give instructions or assignments. Selene reserves the right to amend and change responsibilities to meet business and organizational needs. Privacy Policy - Selene (seleneadvantage.com)

We are seeking a skilled and experienced R&D Technician to join our team at our facility located in Milwaukee, WI, 53224. As an R&D Technician, you will play a crucial role in our research and development efforts, contributing to the design, testing, and improvement of our products (boilers and burners). This is an exciting opportunity to work in a fast-paced manufacturing environment and utilize your electrical and mechanical troubleshooting skills. Responsibilities Conduct electrical troubleshooting to identify and resolve issues in product prototypes and existing designs Perform mechanical troubleshooting to diagnose and fix problems in machinery and equipment Collaborate with the R&D team to develop and test new product concepts and prototypes Assist in the design and modification of existing products to enhance performance and functionality Conduct experiments, collect data, and analyze results to support product development and improvement Maintain accurate documentation of test procedures, results, and any modifications made Assist in the installation, setup, and calibration of equipment and instruments Ensure compliance with safety regulations and protocols during all R&D activities Fabricate special parts or equipment. Qualifications Strong electrical troubleshooting skills, with the ability to diagnose and repair complex electrical systems Proficiency in mechanical troubleshooting, including the ability to identify and resolve mechanical issues in machinery and equipment Prior experience working in a manufacturing environment, preferably in an R&D or product development role Knowledge of HVAC systems and their components a plus Ability to read and interpret technical drawings, schematics, and specifications Excellent problem-solving and analytical skills Strong attention to detail and ability to work with precision Good communication and teamwork skills Ability to adapt to changing priorities and work under tight deadlines You should be proficient in: HVAC Electrical Troubleshooting Skills Mechanical Troubleshooting Skills Experience in a Manufacturing Environment

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. This position will have responsibility for supporting activities in the QC Sample Management group, which includes use of material control procedures and specification documents, raw material sampling & inspection, participation in the coordination of testing with internal and external resources, and collection of data and material certificates for review by QA. Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The essential duties and responsibilities include the following but other duties may be assigned. Review all incoming material receipt packets to assess testing needs Schedule and perform sampling of raw materials across the PCI Madison, WI Sites Request quotes and purchase orders for testing performed externally Assist with regular communications with 3 rd party labs performing external testing Complete and submit all applicable sample submission paperwork to the appropriate testing labs Escalate testing failure or safety concerns to management in a timely fashion Assist in deviation, out-of-specification or aberrant result investigations, as needed Assist with the writing and revision of cGMP documents and Raw Material Specifications documents to meet industry standards Assist with reviewing testing results to ensure accuracy and compliance. Perform routine cleaning of sampling facilities Routinely perform aseptic sampling inside a Biological Safety Cabinet Perform dimensional inspections on packaging components Perform routine data generation and problem solving Order/restock laboratory and office supplies, as needed. Complete assigned training in a timely fashion Special 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. The employee must be physically capable to perform the duties listed below with or without reasonable accommodations which may be made to enable individuals with disabilities to perform the essential functions. Must be able to walk and drive between local sites Must be able to physically wear laboratory protective attire and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves Must be comfortable working with and handling hazardous materials in safety cabinets 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. Laboratory, manufacturing, warehouse Qualifications: The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. 0-3 years relevant business experience Proficient in MS Office. Must have strong attention to detail as well as ability to work in a cross-functional team environment Professional interpersonal skills and the ability to communicate well orally and in in writing Ability to multi-task in a dynamic environment with changing priorities Ability to work independently as well as on a team, with limited supervisory oversight Master Control experience a plus cGMP experience a plus Join us and be part of building the bridge between life changing therapies and patients. Let's talk future Equal Employment Opportunity (EEO) Statement: PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

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

Benefits: * 401(k) * Bonus based on performance * Flexible schedule * Training & development Doping Control Officer I or II (DCO I or DCO II) USADA is seeking a dedicated and driven person to help our organization fulfill its mission to "Stand with athletes to champion their right to clean sport, inspire true and healthy sport, and promote the integrity of sport." This is an incredibly exciting time to join Team USADA, as we continue to grow our Anti-Doping program and work to support major international competitions such as the Olympic and Paralympic Games in 2026 (Milan), and 2028 (Los Angeles). New team members will have the chance to help ensure USADA is well-positioned in the near and long term for these opportunities as we look to the future with our efforts to protect clean athletes. With the 2028 Games on domestic soil, there will also be opportunities and growth potential over the years for USADA team members to underpin the organizing committee's commitment to a clean Games. REPORTS TO: DC Ops Manager & Asst Manager FLSA: Non-Exempt SUPERVISES: N/A Last revised: July 2025 LOCATION: Madison, WI (Must reside w/in 50 miles) Anticipated # of Tests/Year: 10-15 JOB SUMMARY: Responsible for sample collection from athletes. Tasks performed by the Doping Control Officer (DCO) include preparation for, execution of and post-collection administration as it relates to Doping Control both at events and in the out-of-competition setting. DCOs are the field facing representatives of USADA. The primary objective of the DCO is to conduct Doping Control throughout the United States, under direction of the Doping Control Operations team, for Olympic, Paralympic, and Client Services testing teams, in support of USADA's mission and vision. The DCO works with the HQ team to uphold USADA's goals of creating and maintaining a fair and healthy environment for all athletes. The role will include both local and national travel to conduct Doping Control assignments. The following job expectations, responsibilities, and qualifications apply to both the DCO I and DCO II positions, however, in order to qualify for a DCO II level, one must have a valid phlebotomy credential in good standing, as further outlined below. A DCO II is able to serve as a doping control officer that can draw blood. RESPONSIBILITIES: * Conduct sample collection sessions in support of the testing programs for the Olympic/Paralympic, and Client Services testing teams, as well as on behalf of other agencies, when requested by USADA. * Accept, plan and manage doping control assignments, in accordance with the minimum requirements of the WADA/International Standards, and any minimum criteria established by USADA. * Execute logistics aspects as they relate to the doping control process to facilitate successful completion of missions. * Conduct doping control, including processing of Samples, in accordance with USADA's protocols and procedures, and in accordance with the WADA Code/International Standards. * Recruit and onboard independent contractors to serve in the capacity of a Chaperone*. *(Chaperones may be required in the event the athlete is a minor and/or if the gender of the DCO is not the same as the gender of the athlete being tested) * Witness sample collection or overseeing the witnessing of the sample collection process. * Travel (car, plane, train etc.) to various locations to perform sample collections (by the most economical route). * Ensure accurate documentation/completion of the doping control process. * Ship and submit processed Samples to the specified WADA certified laboratory. * Assist in the onboarding and training of new doping control officers. * Accountable to the most current version(s) of the DCO Manual, sample collection. documentation and other training resources. * Participate in DCO evaluation and support program, continuing education and re-accreditation. * Ensure adequate control of document, record and sample collection equipment. * Schedule and manage all travel, as well as associated expense reports. * Provide witness testimony in Legal cases, such as whereabout failures, other Anti-Doping Rule Violations. * Enforce infection control processes at all times that you are working with equipment or athletes. GENERAL: * Maintain confidentiality at all times. * Have no affiliation with sample collection organizations outside of USADA. * Keep USADA aware of issues in the field and/or any conflicts of interest. * Recommend necessary updates and revisions to USADA protocol and procedures as related to Doping Control. * Projects and other duties, as assigned. REQUIRED QUALIFICATIONS: Skills: * Excellent oral and written communication skills. * Excellent organizational skills and attention to detail. * Demonstrated high proficiency in utilizing technology such as tablets, multiple software platforms, and various applications. Demonstrated ability to: * Make decisions in accordance with USADA's protocol and procedures. * Multitask and work accurately under pressure. * Interact with internal and external customers professionally and in line with USADA's values. * Travel, possibly at short notice, to conduct test assignments. * Work flexible hours, as needed. * Access the internet for daily communication. * Values integrity, respect, and justice among internal and external constituents. * Perform effectively and collaboratively in a team environment. * Meet deadlines and operate with limited supervision. * Stand, bend and lift 50 pounds, on a regular basis. Certification: * Successful completion of all USADA certification/recertification requirements. * Pass bi-annual written and practical exams. * Attend DCO training sessions, meetings, conferences. * Valid Driver's License in good standing with state requirements where you reside. * Must be fully vaccinated against COVID-19. DCO II Additional Requirements: * *National Phlebotomy certification from one of the following accredited agencies: * ACA- American Certification Agency (certified on/after July 2003) * AMT -American Medical Technologists (certified on/after April, 2003) * ASCP - American Society of Clinical Pathology (certified on/after June, 2003) * NHA- National Healthcareer Association (certified on/after February 2005) * NCCT/MMCI- National Center for Competency Testing (certified on/after February 2003) * Applicants who are certified before the above dates must re-take the certifying examination. A more advanced, applicable credential such as RN, NP or PA will satisfy this requirement. * CPT I & II in California are acceptable credentials as they require successful completion of a national exam by one of the certifying bodies outlined above. * In addition to a current national certification, individuals will be required to ensure compliance with state specific phlebotomy training requirements for the state in which they reside. * At least 3 years phlebotomy experience, preferred. Additional Certification(s): * Obtain SafeSport Certification (post-offer) DESIRED QUALIFICATIONS: * Work experience in Allied Health Professions w/certification and/or License (Athletic Trainer, Physical Therapist, Registered Nurse, Paramedics, etc.) COMPENSATION & TIME COMMITMENT: * Compensation is on a per-test basis(piece rate) for out-of-competition (OOC) missions, with compensation typically ranging from $130 to $180 per test dependent on the test parameters. OOC test sessions can vary in length, but generally take 1 to 2 hours for successful completion. * In Competition (event) testing is paid at a daily flat rate, typically at $250 per day. * Onboarding is anticipated to begin in December/January with a more significant time commitment up front for training. Expect a time commitment of 24-30 hours of time during the first 60 days of onboarding. After that it should only be 2-3 hours of training and updates per quarter, plus the necessary time to complete test assignments.

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.

The INNIO Advantage: By combining a rich legacy in the power and gas compression space with pioneering technology, INNIO brings our customers affordable, reliable, and sustainable energy solutions for today-and tomorrow. As a very successful company, we are experiencing significant growth in the United States. Today, we help meet the world's energy needs with 64 GW of installed capacity and 48,000 of our powerful Jenbacher and Waukesha engines, which can be found in more than 100 countries. By harnessing our history of energy industry firsts, along with the power of digital innovation, we will continue to deliver for the future. Welcome to a World of Innovation and Inspiration. Welcome to INNIO! The Production Quality Associate for Engine Testing & Painting ensures that all engines meet INNIO's quality standards during the testing and painting phases. This role focuses on process optimization, defect prevention, and continuous improvement to deliver high-quality products. Key Responsibilities: Ensure adherence to quality control processes for engine testing and painting operations. Maintain quality standards, procedures, and documentation for both testing and painting. Monitor and perform inspections and quality checks during engine testing and painting. Conduct root cause analysis for process failures, defects, and non-conformities; implement corrective and preventive actions. Collaborate with production, engineering, and maintenance teams to resolve quality issues and improve process reliability. Participate in audits and continuous improvement initiatives. Support new product introductions and process changes by validating quality requirements. Utilize quality tools such as FMEA, 8D, SPC, and control plans to drive continuous improvement. Report and collaborate on key quality metrics, including defect rates, rework, scrap, and process capability. Ensure compliance with company policies, industry standards, and customer requirements. Qualifications: Education in engineering, manufacturing, or related fields. Experience in quality within manufacturing, preferably engine production and/or industrial painting. Strong knowledge of engine testing procedures and industrial painting processes. Familiarity with quality management systems (ISO 9001 or similar). Proficiency in quality tools and methodologies (FMEA, 8D, SPC, root cause analysis). Analytical mindset with attention to detail. Strong computer skills Excellent communication and teamwork skills. Ability to work independently and manage multiple priorities. #Waukesha INNIO offers a great work environment, professional development, challenging careers, and competitive compensation. INNIO is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, gender (including pregnancy), sexual orientation, gender identity or expression, age, disability, veteran status or any other characteristics protected by law.

Are you ready for a new beginning? We need your talent, knowledge and dedication to better our world with biology. Our purpose points the way In Novonesis, we know that solutions rooted in biology can help solve humanity's biggest challenges. Since we began more than a century ago, this has been our guide. It's how we've gotten so far. And it's how we'll impact the future. Now, more than ever, the world needs change. And with biosolutions, the possibilities for transformation are endless. We're here to better our world with biology. Join us as our new QC Lab Assistant The Quality Control Team ensures Novonesis delivers high-quality products by maintaining strict adherence to quality, safety, and compliance standards. Their work directly supports the company's mission of innovation and customer satisfaction. In this role you'll make an impact by: Collecting samples of raw materials, in-process materials, and finished products in accordance with SOPs. Performing physical inspections of incoming raw materials for cosmetic defects, contamination, and adherence to specifications. Conducting basic physical tests on samples as assigned. Preparing laboratory reagents, media, and test solutions according to established procedures. Verifying and calibrating laboratory and inspection equipment (e.g., scales, pH meters) as scheduled. Reviewing supplier Certificates of Analysis (COAs) against internal specifications and report discrepancies. Recording and tracking samples and test data in laboratory databases (e.g., LIMS, SAP) with accuracy and attention to detail. Communicating any non-conformances or deviations identified during testing or inspection to QC management. Maintaining cleanliness and organization of lab and sampling areas in accordance with GMP and 5S standards. To succeed you must hold: 1 to 3 years in Quality Control or Quality Assurance Ability to read, write, and speak English. Excellent oral and written communication skills; able to professionally communicate across departments and with auditors as needed. Strong understanding of Good Manufacturing Practices (GMP), quality systems, and compliance requirements. Ability to read, understand, and follow Standard Operating Procedures (SOPs), Work Instructions, safety rules, and technical documentation. Proficient in performing and interpreting basic mathematical functions and ability to work with metric units (e.g., mL, °C). Strong observational skills with keen attention to detail and accuracy. Able to operate a variety of laboratory equipment and instruments, as well as standard office equipment. Capable of managing multiple, changing priorities and responding to unanticipated issues without losing focus on core responsibilities. Strong problem-solving and critical thinking skills; able to interpret written, oral, diagram, or schedule instructions effectively. Location: Wausau, WI (On-Site) Application deadline: 1/30/26 Expected salary: $21 an hour Benefits you will enjoy: 401(k) with up to a 9% company contribution Minimum of 3 weeks of vacation plus 12 holidays and 2 weeks of Wellness Time Health, Dental, Vision & Life insurance Healthcare savings account option Employee assistance program Parental leave Tuition reimbursement All benefits begin on your first day Could our purpose be yours? Then apply today! At Novonesis we commit to an inclusive recruitment process and equality of opportunity for all our job applicants. We recommend you not to attach a cover letter to your application. Instead, please include a few sentences in your resume/CV about why you are applying. To ensure a fair recruitment process, please refrain from adding a photo in your resume/CV. Novonesis is dedicated to fostering a unique community by embracing and respecting differences. We make all employment decisions based on business needs, ensuring that every individual can thrive, regardless of identity or background such as ethnicity, religion, gender, sexual orientation, age, disability, or veteran status. Want to learn more? Learn more about Novonesis, our purpose, and your career opportunities at novonesis.com Not the right fit for you? Even if this job isn't the right fit for you, perhaps you know someone who might find it interesting. If so, please feel free to share the job link and encourage them to apply. Thank you for your referral! Please check out our other open positions. The right fit for you could just be a few clicks away. Stay alert: Avoid recruitment scams At Novonesis, we are committed to maintaining a safe and transparent recruitment process. Please be aware of potential scams targeting job seekers and take note of the following: Novonesis will never ask for sensitive personal information, such as bank account details, Social Security numbers, or passwords, at any stage of the hiring process. Novonesis does not make employment offers without conducting interviews with candidates. If you receive suspicious communication claiming to be from Novonesis, please do not share any personal or financial information. We encourage you to verify the legitimacy of the message by contacting us directly through our official channels.

Conduct the appropriate testing and quality inspections of all products thoroughly to ensure that our customers' standards are met. ESSENTIAL DUTIES AND RESPONSIBILITIES: Verify quality and maintain records for all raw materials to ensure the product meets vendor specifications prior to use in finished goods Perform tests on all products to ensure customers' requirements are met. Perform quality inspections at start-up to match quality pack standards and then regularly during the filling of the order to ensure that the quality of the product is still being met. Maintain proper documentation within the Quality Department and Production. Other duties as assigned Requirements EDUCATION, TRAINING & EXPERIENCE: Previous production experience preferred On the job training provided SKILLS, KNOWLEDGE & ABILITIES: Must possess good written and verbal communication skills. Must be self-motivated, detail oriented, and precise in their daily duties. Ability to function cooperatively and effectively in a team environment with peers and personnel in other departments Ability to keep company and customer information that is discussed or viewed while under employment with Truvant confidential Ability to adhere to all regulatory and company policies, procedures, work instructions including but not limited to: Truvant policies, customer specific policies, ISO, GMP's, USDA, regulatory food safety and food defense PHYSICAL AND ENVIRONMENTAL REQUIREMENTS: Must be able to read documents, printouts, computer screens and other communication Must be able to hear well enough to communicate with co-workers Must be able to reach, touch, grasp Must be able to stand and/or walk for prolonged periods of time Must be able to climb, stoop/kneel, lift, pull and push Must be able to conduct yourself in a safe manner to avoid accidents while on the production floor Must be able to work in various environments based on building location and products. Level of Physical Requirements: Sedentary to medium work level; lifting and positioning weight loads up to 35 pounds TRAVEL REQUIREMENTS: 0% - Optional travel may be offered to support business needs

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