Quality control inspector jobs in Eau Claire, WI - 864 jobs

We are looking for 3rd shift availability. Shift hours are Friday through Sunday 5am to 5pm. • Coordinate between Veritas Steel Production and DOT Inspectors to ensure DOT witnessing of production operations and QC hold points are being completed. • Perform visual inspection of material as required. • Perform layout checks as needed. • Perform rotational capacity tests on bolts prior to use in shop. • Work with outside inspectors to resolve quality issues on the floor. • Monitor welder qualification tests. • Monitor and record welding parameters to insure compliance to approved WPS. • Be able to read and understand the Welding code and Specifications. • Perform Dimensional checks on lay downs and shop assemblies. Use Total Station as needed. • Develop improvements in the quality control process to facilitate flow of work through shop. Primary Responsibilities: How will you accomplish the Objectives? • Perform in a manner that will assure quality work flowing through the shop. • Work with welders and leadmen to maintain quality. • Be available, by use of a radio, etc. to perform needed checks. • Maintain a log of work done, and complete required reports. • Interpret the Specifications and applicable Codes. • Ability to be flexible to work either early or late within assigned shift as needed. • Coordinate inspection of QC hold points between production and DOT Inspectors. • Use and encourage safe working habits. Must have CWI Certification NACE or BCI Certification is desired Ability to be conscious of Specifications and Company standards Ability to be organized and precise in maintaining a diary and reports Must have good people skills in dealing with difficult situations Ambitious person to help meet department and company goals and schedule. Competencies/Skills To perform the responsibilities, you must have the ability and skills to: • Effectively communicate with the crews, supervisors, and Quality Manager the results of your work, evaluate problems, proposed acceptable corrections, solutions, and schedules. • Coordinate your work with shipping department to assure loads have been inspected and ready to ship. • Work with supervisors to plan your work and time in each shop to facilitate the flow of quality work through the shop. • General working knowledge of Total Station to assist crews as needed and finalize assemblies during off shifts as needed. Measures of Success: Objective facts that demonstrate great performance. • Outstanding work record, great attendance record and always-on time. • No accidents. A safe worker is an asset to both their fellow worker and the company. • Increase throughput in the area that work being performed being able to streamline the required work and constantly making positive improvements. • Accept positive feedback from fellow workers and supervisors, on performance and competencies. HOURS - Friday - Sunday 5am - 5pm

Salary: Based on skills and experience Schedule : 5pm-5:10am on a 2-2-3 rotation, including every other weekend We are looking to add a Quality Assurance Technician to our water bottling plant to carry out our company mission of maintaining an inclusive culture of trust, honesty, humility, integrity, and candor in our dealings with others, ourselves, and our communities. Who are we? Premium Waters is the 2nd largest bottler of private label bottled water products in the U.S.A. We are committed to providing high quality bottled water in an environmentally friendly manner. Our Teams focus on proactively supporting safety, understanding sustainability, and building lasting relationships. Your part in our story: The QA Tech is responsible for conducting micro testing, wet chemical analysis of water, testing and maintaining the RO, enforcing GMP policies, quarterly CFR testing for bottles and closures, and various other tasks as they arise. Responsibilities include: Performs daily and quarterly micros Performs wet chemical analysis of product. Performs Quality checks and calibrations. Maintains quality forms and may do cleaning. Performs daily Plant checks/walkthrough checking Presage quality checks and cleanliness. Writes Process deviations and Non-Conformances. Over sees corrective actions are being implemented Makes sure that Plant personnel are adhering to corporate GMP policies Maintains chemical inventory Must be able to communicate at all levels Must follow all established Good Manufacturing Practices. Work 5am-5:10pm on a 2-2-3 shift schedule: Work: Monday & Tuesday - Off: Wednesday & Thursday - Work: Friday, Saturday & Sunday Off: Monday & Tuesday - Work: Wednesday & Thursday - Off: Friday, Saturday & Sunday Why work with us? We strive to foster an environment that celebrates differences in our teams at all PWI locations. We recognize that a diverse and inclusive workforce results in better decision-making, faster and more innovative problem solving, and creates a safe and welcoming environment for everyone. Benefits include: Medical, Prescription Drug, and Vision Program -on DAY ONE Dental - on DAY ONE A generous PTO program -112 hours in your first year! Paid Parental Leave Gym Reimbursement Program and Company Paid Wellness Coach Online Virtual Care Company Paid Life Insurance for Employee, Spouse, Children Company Paid Long and Short-Term Disability Company Paid Employee Assistance Program Flexible Spending Account Education/Tuition Reimbursement Program - to supplement your current skillset or advance to a higher position. 401(K) - Company Match 100% up to 4% Bereavement Leave Volunteer Time Off Program Holiday Pay Employee Water Program - Free Water Referral Bonus Daily Pay FREE physical therapy on site FREE employee medical care at our near-site clinic starting on 1/1/26 About you - preferred requirements for this role High School diploma or equivalent, undergraduate degree preferred Food, beverage, or liquid consumer product manufacturing a plus. Ability to work a flexible schedule as needed Basic reading, writing, and math skills Functional Knowledge of Excel, Word, Power Point Excellent verbal and written communication skills Safety - Everyone at Premium Waters, Inc. must be involved and committed to safety. This must be a team effort. Together, we can prevent accidents and injuries and keep each other safe and healthy in the work that provides our livelihood.

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.

rms Company provides contract manufacturing of high-quality, tight-tolerance medical implants, components and sub-assemblies using cutting-edge technology. rms is part of the Cretex Medical family of companies. Learn more at ******************** and ********************** Quality Inspector Position Summary The Quality Inspector supports the production floor & reports to the Production Supervisor, ensuring product compliance to quality and industry specifications. 1st Shift: Monday - Friday 6:00am - 2:30pm Responsibilities Quality Inspector Responsibilities: * Conduct mechanical and visual inspections, reporting and isolating non-conforming product * Perform in-process inspections and document findings as required * Inspect finished products to determine conformance through inspections to specifications; conducting visual and dimensional testing; creating rejections for nonconforming products and confirming re-work. * Perform and document inspection results through paperwork review, completion of IP forms (inspection plan documents), enter data into data base when required, create shipping packets * Communicate quality issues to Supervisor Qualifications Desirable Requirements/Qualifications: * High school diploma or equivalent * 1 year of experience in a manufacturing environment * Understanding of ISO 13485 * Experience with measurement and testing equipment * Vision System experience a plus * Proficient in blue print reading rms Company Benefits As a Cretex Medical company, rms offers a full benefit package to its employees. Benefits include medical, dental, vision and life insurance options. rms also offers a 401(k) retirement plan with employer match, profit sharing, short- term and long-term disability insurance, paid time off, holiday pay, and an onsite medical clinic. rms Company also offers company specific benefits, such as: * Onsite Clinic * Paid Parental Leave * Monthly Social Events * Annual Employee Appreciation Week * Volunteer Opportunities * Training and Development Opportunities * Tuition Reimbursement * Wellness Program Cretex Companies use cutting oils, solvents, and other chemicals in the manufacturing process. Testing is conducted on a periodic basis to ensure that all chemicals are kept well below the OSHA permissible exposure levels. Pay Range USD $17.75 - USD $24.09 /Hr. Pay Range Details This pay range reflects the base hourly rate or annual salary for positions within this job grade, based on our market-based pay structures. Actual compensation will depend on factors such as skills, relevant experience, education, internal equity, business needs, and local market conditions. While the full hiring range is shared for transparency, offers are rarely made at the minimum or maximum of the range. Company Benefits All Employees: Our 401k retirement savings plan with a company match contribution; onsite health clinics, discretionary holiday bonus program (based on years of service), Cretex University, 24/7 employee assistance program with access to five confidential visits with a licensed counselor at no cost, wellness program with incentives, an employee death benefit, and employee sick and safe leave are available to all Cretex employees. 20+hours: Cretex's medical benefit package includes: comprehensive medical insurance with access to virtual providers; dental insurance (Little Partners Dental benefit covers services 100 percent for children 12 and younger when seen by a Health Partners in network provider); vision insurance; a pre-tax health savings account, healthcare and dependent care pre-tax reimbursement accounts; paid holidays, paid time off; and our discretionary profit sharing program are available to employees working 20+ hours/week. 30+ hours: Parental Leave, accident and critical illness benefits, optional employee, spouse, and child life; short and long term disability; company provided life insurance; and tuition assistance programs are available to employees working 30+ hours per week. (Some benefits are subject to eligibility criteria.) Applicants will receive consideration for employment regardless of their race, color, creed, religion, national origin, sex, sexual orientation, gender identity, disability, age, veteran status, marital status, family status, status with regard to public assistance, or any other protected status as required by law. Our company uses E-Verify to confirm the employment and eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit *********************

Electric Machinery Company, a division of WEG Electric Corp. Minneapolis, MN Quality Inspector / Electrical Manufacturing - 1st Shift Department: Quality Team Department Responsible for acting in the quality control process, performing activities such as visual and dimensional inspection of parts, and other activities. Major Areas of Accountability WEN: Inspect parts or products using appropriate instruments, following pre-established standards and procedures, and guide other inspectors in their activities. Conduct nondestructive tests, including visual inspection, liquid penetrant testing, magnetic particle testing, and ultrasonic testing. Interpret specifications relevant to your area of activity, such as standards, product drawings, electromechanical specifications, and catalogs. Compare inspection results with specification values, making decisions on acceptance or rejection based on conformity. Perform inspections on special products, monitor them, and address any issues that arise. Analyze customer purchase orders, drawings, specifications, standards, and modifications to ensure product conformity and verify quality assurance conditions. Coordinate with support areas (e.g., Sales, Product Engineering, PCP, Purchasing) to assess product and material conformity. Identify inspected items with appropriate labels and inform the production area leader if necessary. Prepare inspection reports detailing the quality of parts, finished products, or in-process items, highlighting relevant findings. Calibrate measuring instruments and devices using reference standards for various inspections. Maintain data on quality issues related to non-conformance. Commit to Continuous Improvement by identifying and acting on opportunities in daily work. Adhere to ISO 9001 Quality Standards and comply with OSHA and EPA regulations. Knowledge, Skills, and Abilities Education and Experience: High School Diploma or equivalent required; advanced certification or degree in a related field preferred. Ability to read and interpret blueprints, including geometric tolerances, and specifications (e.g., process specifications, NEMA, IEEE, ASTM, ASME, API). Knowledge of welding, machining, painting, and assembly processes. Proficiency in shop math for calculating dimensions such as bolt circles, chords, tapers, thread forms, and true position. Desired computer skills; experience with SAP system or vibration software (e.g., ADRE) is a plus. Ability to work independently with minimal supervision and be self-motivated. Effective teamwork and independent work skills. Strong oral and written communication skills. Ability to partner and communicate effectively with internal and external customers at all organizational levels. Ability to follow written inspection plans. Salary: 1st shift salary range $21.00 hourly to $25.00 hourly Will compensate with experience. Position is full-time. Pay Types Voluntary weekend overtime. Saturday is paid at time and a half, Sundays are paid at double time! Benefits: Medical, Dental & Vision Insurance eligible your 1st day on the job 401K with Match 1st month following hire Quarterly Bonus Program payout potential Company paid Holidays (12) and Paid Birthday (1) (use anytime throughout the year) Paid Time Off (PTO) available immediately Company paid Short- & Long-Term Disability Company paid Life Insurance $6,000 annual Tuition Reimbursement program Company provided tools Company provided uniforms (laundered) Company reimbursement for Safety Shoes & Safety Glasses Secure, onsite free parking Physical Requirements: Routinely lift and move objects up to 20 lbs. Occasionally lift and move objects up to 50 lbs. Occasionally ascend/descend ladders and stairs. Occasionally work at heights or on platforms. Occasionally work in low, tight, or confined spaces. Routinely stand or sit for extended periods. Occasionally use repetitive motions (e.g., wrists, hands, fingers) to operate machinery or tools. Occasionally operate machinery and power tools. Routinely move between workstations to complete tasks. Company cannot provide sponsorship for this position Please, no agencies

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

PCB Manufacturing | QC Inspector Scope: Inspect and evaluate final products to ensure compliance to customer requirements prior to delivery. Essential Job Function: Be able to complete AS 9102 Reports Perform Final Inspection on finished product to ensure compliance to customer requirements. Read customer drawings Perform measurements with measurement tools such as calipers, micrometers, and pin gages. Perform rework as appropriate, which may include mask touch-up, material removal with an x-acto knife, burnishing, soldering irons, final finish brush plating, sanding Verify acceptability of rework after completion Identify and mark non-conforming product to ensure it is not delivered Prepare standard and AS9102 First Article Reports as needed Verify certifications and reports are complete and accurate and can be used for final acceptance and certification of product Complete Deliverables for Customers and ensure they are complete and accurate Complete department logs and record yield data as required Perform preventative maintenance as defined by department maintenance schedule Support other work areas or departments as required by production or management. Ability to work overtime as requested Keep work area clean and organized Requirements Essential Qualifications, Education and Experience: High school diploma or equivalent One year of Quality Control experience Knowledge of AS 9100 Strong work ethic Ability to work effectively in a team environment Physical Requirements: Prolonged periods sitting and performing visual and manual tasks. Fine motor skills Ability to use microscopes for long periods of time performing job duties AdvancedPCB is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, status as a protected veteran, marital status, genetic information, medical condition, or any other characteristic protected by law (EEOC).Compensation: Exact compensation may vary based on skills, experience, and location. About AdvancedPCB, AdvancedPCB is a leading manufacturer of high-reliability printed circuit boards. The company features 6 total manufacturing sites: Santa Clara, our headquarters in the heart of the Silicon Valley; 2 in Southern California, 1 in Maple Grove, Minnesota, Aurora, Colorado and Chandler Arizona. Currently, the company is viewed as over $100 Million; 180,000 sq. ft. of manufacturing space with over 480 employees, making APCT one of the largest privately held printed circuit board manufacturers in North America. Visit us!********************* Salary Description $20-$25.00/hour

Cadrex is searching for a Quality Technician III to directly support our manufacturing practices through development, evaluation, and continual improvement of processes using quality concepts, principles, and methodologies with the goal of consistently meeting or exceeding customer expectations of quality. KEY RESPONSIBILITIES Release product for shipping by ensuring proper documentation/certifications are provided as outlined by customer requirements Understand and apply basic GD&T concepts Proficient in dimensional verification of PPAP and first article parts Provide direct support to the production floor by assisting with interpretation/development of manufacturing related documentation and providing or teaching proper measuring techniques Provide technical inspection of manufactured and raw materials at “receiving” as outlined by the process Collect data, evaluate, and present quality metrics Program and operate FARO & Micro-Vu measurement equipment proficiently Attend department meetings as required Prioritize work order tasks for QA lab Audit internal processes including dimensional workmanship and documentation verification Develop calibration procedures and provide calibration of measuring equipment as outlined by ISO standards Work to establish closed loop cause and corrective action in reaction to customer complaints and internal process failures Trained and efficient in all aspects of the position Work quickly, efficiently, and without quality issues Provide on-the-job training for new quality inspectors with daily responsibilities Support management through implementing and communicating ideas, projects, practices, and decision outcomes to the Quality team? Suggest and complete Continuous Improvement Projects Guide, train and develop new hires in Quality Lab for all aspects of the position including work center tasks and Quality tools Administer employee development training for the QA department Lead or participate in Quality Walk Audits in Work Center Areas identify and implement continuous improvement process and project improvements Requirements PREFERRED QUALIFICATIONS 5+ years working preferably in a metal fabrication environment under a continuous improvement QMS with hands on inspection or an equivalent combination of education and experience Read and comprehend simple instructions, short correspondence, and memos. Write simple correspondence Effectively present information in one-on-one and small group situations to customers, clients, and other employees Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals Ability to compute rate, ratio, and percentage and to draw and interpret graphs Knowledge of word processing software, spreadsheet software, e-mail software and the use of the Internet Certification as a Quality Technician preferred Programming for FARO and Micro-Vu Measurement Equipment desired EDUCATION Associate degree in related field preferred LOCATION Onsite SCHEDULE M-Th; 6:00AM - 4:30PM WORK ENVIRONMENT While performing the duties of this job, the employee is frequently exposed to work near moving mechanical parts and vibration. The employee is occasionally exposed to the risk of electrical shock. The noise level in the work environment is usually moderate and occasionally loud. PHYSICAL DEMANDS While performing the duties of this job, the employee is regularly required to stand, sit, use hands and fingers, handle or feel, and talk or hear. The employee is occasionally required to sit; climb or balance; stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, peripheral vision, color vision, depth perception and ability to adjust focus. CADREX'S CORE VALUES Safety first, rising to the challenge, collaboration, accountability, and doing the right thing TOTAL COMPENSATION INCLUDES Health/dental/vision coverage Employer-paid and supplemental life insurance Short- and long-term disability insurance Generous paid time off and holiday pay Monthly remote work stipend (for remote employees who qualify) 401(k) investment plan, with an employer match of up to 4% Education support program Safety eyeglasses/shoe reimbursement Referral bonuses Bonus plan for all full-time employees ABOUT US CADREX Manufacturing Solutions is a leading provider of complex sheet metal and machined production parts, assemblies, and weldments for a variety of end markets, including electrical transmission and distribution, warehouse automation, technology, aerospace & defense, medical, food, and industrials. With locations in Colorado, Pennsylvania, Illinois, Washington, Wisconsin, Minnesota, Michigan, Indiana, Massachusetts, Oklahoma, and Monterrey Mexico, CADREX offers numerous in-house manufacturing capabilities, including laser cutting, sheet metal fabrication, complex assembly, CNC punching, CNC machining, forming, robotic welding, stamping, fastener insertion, and tool and die manufacturing, to effectively serve customers with lights-out manufacturing capabilities for mid- to high-volume production. For more information, visit *************** Cadrex provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Medical Cretex Medical is a leading contract manufacturer of precision components and assemblies for the medical device industry. Our customers view us as a trusted partner in the areas of injection molding, laser processing, metal stamping and device assembly. Learn more at ********************** Quality Inspector Position Summary The Quality Inspector performs first piece, in-process inspections, and final inspections of components and assemblies per control/quality plans. The Quality Inspector will review and approve final release documentation. Performs incoming inspections per control/quality plans for received materials. This role will also complete appropriate quality records within company and GMP guidelines, policies and procedures. Shifts Available: 9th: 6:00pm-6:30 am Thurs-Sat, every other Sunday Responsibilities Inspection of injection molded parts relating to quality, appearance and performance Inspection of assemblies relating to quality, appearance and performance Inspection of received materials relating to quality, appearance and performance Inspection and audit of final product documentation prior to release Determine reasons for defects Read and understand quality control plans, blueprints and specifications Check parts dimensionally by using precision testing equipment, including Tool Scope, CMM, OGP and various other metrology tools and equipment Effective organizational, oral and written communication skills Read and comply with work instructions, set up sheets, and checklists Accurately records and reports hours worked Maintain an organized work area (5S) to include workstations, equipment, walkways, and locker areas Participate in the Operational Excellence Program Understand and comply with the Cretex professional competencies, company policies, and employee manual Adhere to all safety policies; includes wearing personal protective equipment when Support and complies with the company's Quality System, ISO, and medical device requirements Complete all other work duties as assigned Qualifications Basic knowledge of inspection equipment use and maintenance Read and comprehend customer supplied drawings and specifications Communicate inspection results with team members Manage multiple requirements and deadlines Quickly shift priorities in support of production inspection needs High school diploma or equivalent degree (GED) Experience with measuring instruments, methods and practices including hand tools and machine devices including CMM and Vision Systems Basic knowledge of Microsoft Office (Outlook, Word, Excel) Ability to read, comprehend, follow and document work instructions, standard operating procedures, and training documents Mechanical aptitude Dexterity and hand and eye coordination Attention to detail Strong problem-solving skills Ability to prioritize work and manage multiple tasks Quality Inspector Preferred Knowledge, Skills and Abilities Knowledge of ISO 9001/13485 Quality training/certifications What is it like to work at Cretex Medical? We recognize the contribution of every individual and promote growth, safety and security for all our employees. Cretex Medical values performance and pays competitive wages along with a rich benefit package. We offer a positive work environment with a focus on continuous improvement. Here are some of things that employees have said about working for Cretex Medical: “The culture at Cretex is collaborative. Everyone here is willing to help you whether it is a director, a machinist, or your boss. Everyone is always willing to help you figure out a project and get it done right.” “I would tell potential interns that Cretex is a great company to work for. It has set a high bar for corporate culture as well as the quality of work you can do. I would definitely recommend it.” “I learned that I really like the medical device industry. The importance and the gravity of what we do here is felt by the employees. You can have that passion in your work because you know what you are striving for is to save lives.” We encourage you to explore the many opportunities Cretex Medical can offer you as a valued team member. Pay Range USD $18.00 - USD $26.49 /Hr. Pay Range Details This pay range reflects the base hourly rate or annual salary for positions within this job grade, based on our market-based pay structures. Actual compensation will depend on factors such as skills, relevant experience, education, internal equity, business needs, and local market conditions. While the full hiring range is shared for transparency, offers are rarely made at the minimum or maximum of the range. Company Benefits This position is eligible for shift differential. Pay Range Details: Quality Inspector I- $18.00-$24.09 Quality Inspector II- $18.89-$26.49 All Employees: Our 401k retirement savings plan with a company match contribution; onsite health clinics, discretionary holiday bonus program (based on years of service), Cretex University, 24/7 employee assistance program with access to five confidential visits with a licensed counselor at no cost, wellness program with incentives, an employee death benefit, and employee sick and safe leave are available to all Cretex employees. 20+hours: Cretex's medical benefit package includes: comprehensive medical insurance with access to virtual providers; dental insurance (Little Partners Dental benefit covers services 100 percent for children 12 and younger when seen by a Health Partners in network provider); vision insurance; a pre-tax health savings account, healthcare and dependent care pre-tax reimbursement accounts; paid holidays, paid time off; and our discretionary profit sharing program are available to employees working 20+ hours/week. 30+ hours: Parental Leave, accident and critical illness benefits, optional employee, spouse, and child life; short and long term disability; company provided life insurance; and tuition assistance programs are available to employees working 30+ hours per week. (Some benefits are subject to eligibility criteria.) Applicants will receive consideration for employment regardless of their race, color, creed, religion, national origin, sex, sexual orientation, gender identity, disability, age, veteran status, marital status, family status, status with regard to public assistance, or any other protected status as required by law. Our company uses E-Verify to confirm the employment and eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit *********************

Anteris is a science-driven structural heart company that is redefining expectations and advancing the field through cutting-edge solutions focused on restoring native-like physiology versus treating symptoms of structural heart disease. We are currently developing a new class of TAVR designed to mimic the performance of a healthy aortic valve. With offices in Minneapolis, MN, US; Geneva, Switzerland; and Brisbane and Perth, Australia, we have a growing and inclusive team. The Quality Control Inspection team plays a key role supporting our manufacturing operations at the Maple Grove site. This role is involved in a wide range of inspection tasks, where the primary goal is to assure that the products we produce are conforming to specifications and properly evaluated for compliance to visual, dimensional, functional, and various other specified requirements. The QC Inspector will be responsible for performing inspections in a highly regulated medical device development and manufacturing environment across all areas of standard work for the team (receiving inspection, first article inspections, label verifications, valve inspections, tissue inspections, pre-sterile product inspections, and sterile product inspections). This is a high visibility role with daily interactions across a wide range of peer groups in the Maple Grove site. Shift: Day Shift, Monday through Friday, 6:00 a.m. - 2:00 p.m. At Anteris Technologies, you'll be part of a team dedicated to enhancing the quality of life for patients with aortic stenosis through groundbreaking medical devices. Join us in our mission to revolutionize structural heart solutions. Primary Duties and Responsibilities Perform all duties listed below in strict compliance with the Anteris Quality Management System including Good Documentation Practices. * Responsible for performing receiving inspection on material / products supplied to Anteris to ensure conformance to requirements and specifications. * Perform microscope and other aided visual inspections on biological tissue based medical device products to ensure conformance to processing requirements and specifications. * Perform machine / software-controlled inspections on products to ensure conformance to processing requirements and specifications. * Perform inspections, as required by procedure, in support of first article inspections and label verifications. * Perform physical and visual inspections on material, products, and/or packaging being processed for sterilization. * Make an informed decision, based on training to tasks assigned, on the acceptance of materials, products, and inspected features, requirements, and specifications in all standard work tasks. * Complete and maintain accurate records of inspection activities, including measurements, observations, results, conclusions, nonconformance issues, and full completion of quality record fields in support of standard work tasks. * Collaborate with peers in Operations to effectively stay on plan, be mutually organized to goals, and communicate effectively through escalation channels as required. * Other tasks assigned by group lead or designee. Skills, Knowledge, Experience & Qualifications Required Skills and Knowledge: * High School diploma or equivalent. * 2+ years' overall experience in Medical Device (ISO 13485, FDA QSR) manufacturing environment. * 1+ year's equivalent work experience directly applicable to Primary Duties and Responsibilities listed above. * Strong attention to detail and experience in reading, interpreting, and comprehending product requirement documents and specifications. * Experience in learning and cross-training on widening set of responsibilities in a team-based environment. * Experience working directly with computers to input data, perform electronic based work tasks, complete training, and manage email communications. * Effective verbal and written communication * Ability to work in a fast-paced environment. * Effective problem-solving and troubleshooting skills. Preferred Skills and Knowledge: * Vocational or technical training in assembly, sewing, or inspection of biological tissue based medical devices. * Vocational or technical training in the use of microscopes, including the use of specialized reticles and/or tappi charts. * Vocational or technical training in the use of MicroVu optical inspection systems. * Vocational or technical training in Lean or 5S principles. * Vocational or technical training in GD&T principles and specification designs. What We Offer: * Opportunity to make a significant impact on the healthcare industry by advancing groundbreaking therapies. * Collaborative and dynamic work environment with a culture of innovation and excellence. * Competitive compensation package, including salary, performance-based bonuses, and stock options. * Career development opportunities and a chance to be part of a growing company that values its employees. Health and Wellness Offerings: * Medical, Dental, and Vision Plans * Flexible Spending Account (FSA) * 401k + Company Match * Life, AD&D, Short Term and Long-Term Disability Insurance * Bonus Plan Eligibility * Employee Equity Program * Paid Holidays & PTO * Employee Assistance Program * Inclusive Team Environment Note: We may require proof of COVID-19 vaccination to comply with the state, local municipality, and/or travel regulations. Anteris Technologies recruits, employs, trains, compensates and promotes regardless of race, religion, color, national origin, sex, disability, age, veteran status, and other protected status as required by applicable law. We have a clear vision: to be a place of belonging for all humans by promoting diversity, multiculturism and inclusion, as a goal and reflection across the organization. Diversity is more than a commitment - it is part of our mission to deliver the best structural heart products on a global scale. By applying to this position, you consent to receive text messages from the Anteris Talent Acquisition team regarding your application. Message and data rates may apply. You may opt out at any time by replying STOP.

Anteris is a science-driven structural heart company that is redefining expectations and advancing the field through cutting-edge solutions focused on restoring native-like physiology versus treating symptoms of structural heart disease. We are currently developing a new class of TAVR designed to mimic the performance of a healthy aortic valve. With offices in Minneapolis, MN, US; Geneva, Switzerland; and Brisbane and Perth, Australia, we have a growing and inclusive team. The Quality Control Inspection team plays a key role supporting our manufacturing operations at the Maple Grove site. This role is involved in a wide range of inspection tasks, where the primary goal is to assure that the products we produce are conforming to specifications and properly evaluated for compliance to visual, dimensional, functional, and various other specified requirements. The QC Inspector will be responsible for performing inspections in a highly regulated medical device development and manufacturing environment across all areas of standard work for the team (receiving inspection, first article inspections, label verifications, valve inspections, tissue inspections, pre-sterile product inspections, and sterile product inspections). This is a high visibility role with daily interactions across a wide range of peer groups in the Maple Grove site. Shift: Day Shift, Monday through Friday, 6:00 a.m. - 2:00 p.m. At Anteris Technologies, you'll be part of a team dedicated to enhancing the quality of life for patients with aortic stenosis through groundbreaking medical devices. Join us in our mission to revolutionize structural heart solutions. Primary Duties and Responsibilities Perform all duties listed below in strict compliance with the Anteris Quality Management System including Good Documentation Practices. Responsible for performing receiving inspection on material / products supplied to Anteris to ensure conformance to requirements and specifications. Perform microscope and other aided visual inspections on biological tissue based medical device products to ensure conformance to processing requirements and specifications. Perform machine / software-controlled inspections on products to ensure conformance to processing requirements and specifications. Perform inspections, as required by procedure, in support of first article inspections and label verifications. Perform physical and visual inspections on material, products, and/or packaging being processed for sterilization. Make an informed decision, based on training to tasks assigned, on the acceptance of materials, products, and inspected features, requirements, and specifications in all standard work tasks. Complete and maintain accurate records of inspection activities, including measurements, observations, results, conclusions, nonconformance issues, and full completion of quality record fields in support of standard work tasks. Collaborate with peers in Operations to effectively stay on plan, be mutually organized to goals, and communicate effectively through escalation channels as required. Other tasks assigned by group lead or designee. Skills, Knowledge, Experience & Qualifications Required Skills and Knowledge: High School diploma or equivalent. 5+ years' overall experience in Medical Device (ISO 13485, FDA QSR) manufacturing environment. 5+ years' equivalent work experience directly applicable to Primary Duties and Responsibilities listed above. Strong attention to detail and experience in reading, interpreting, and comprehending product requirement documents and specifications. Experience in learning and cross-training on widening set of responsibilities in a team-based environment. Experience working directly with computers to input data, perform electronic based work tasks, complete training, and manage email communications. Effective verbal and written communication Ability to work in a fast-paced environment. Effective problem-solving and troubleshooting skills. Preferred Skills and Knowledge: Vocational or technical training in assembly, sewing, or inspection of biological tissue based medical devices. Vocational or technical training in the use of microscopes, including the use of specialized reticles and/or tappi charts. Vocational or technical training in the use of MicroVu optical inspection systems. Vocational or technical training in Lean or 5S principles. Vocational or technical training in GD&T principles and specification designs. What We Offer: Opportunity to make a significant impact on the healthcare industry by advancing groundbreaking therapies. Collaborative and dynamic work environment with a culture of innovation and excellence. Competitive compensation package, including salary, performance-based bonuses, and stock options. Career development opportunities and a chance to be part of a growing company that values its employees. Health and Wellness Offerings: Medical, Dental, and Vision Plans Flexible Spending Account (FSA) 401k + Company Match Life, AD&D, Short Term and Long-Term Disability Insurance Bonus Plan Eligibility Employee Equity Program Paid Holidays & PTO Employee Assistance Program Inclusive Team Environment Note: We may require proof of COVID-19 vaccination to comply with the state, local municipality, and/or travel regulations. Anteris Technologies recruits, employs, trains, compensates and promotes regardless of race, religion, color, national origin, sex, disability, age, veteran status, and other protected status as required by applicable law. We have a clear vision: to be a place of belonging for all humans by promoting diversity, multiculturism and inclusion, as a goal and reflection across the organization. Diversity is more than a commitment - it is part of our mission to deliver the best structural heart products on a global scale. By applying to this position, you consent to receive text messages from the Anteris Talent Acquisition team regarding your application. Message and data rates may apply. You may opt out at any time by replying STOP.

Job Description Product Quality Inspector - Contract (6-9 Months) Schedule: Full-time, 40 hours/week 7-4 Pay: up to $28/hour We have partnered with the Industry leader in cake decorations in the north metro and seeking a Product Quality Inspector. They are in the process of removing synthetic dyes from their edible products and replacing the dyes with natural substitutes that perform different than synthetic dyes. This requires a significant amount of testing for all edible product lines. Ideally someone with quality control, product testing, stability, or quality assurance experience. Key Responsibilities: • Design and execute product testing parameters • Document results in Excel and report findings • Collaborate with QA, R&D, and Product Safety teams Qualifications: • Minimum 1 year of experience in quality control, stability, or QA (3-5 years preferred) • Associate's degree or higher preferred • Proficient in Microsoft Office (Excel, Word, Outlook, Teams; Monday.com is a plus) • Must not be color blind • Food industry experience is a plus Ready to make an impact in a fast-paced, innovative environment? Apply now to be part of an innovative team driving product excellence!

Job Description Why Kendall Howard? We're a growing IT manufacturer with a no-nonsense attitude: stay humble, work hard, and take on challenges head-first. Around here, you won't just “do your job” - you'll be part of a team that builds, solves, and delivers products we're proud to put our name on. The benefits and pay are solid, but the real perk is being part of something that matters alongside people who care just as much as you do. Our Benefits We know benefits matter, and we've got you covered. Full-time employees enjoy: Medical, Dental & Vision coverage Supplemental insurance options 401(k) with company match Paid Time Off (PTO) Paid holidays Job Summary: The Quality Control Inspector is accountable for the practical application of the internal Quality Control System. This position ensures that the quality standards as defined by the designers are being met on the shop floor as well as with materials and services supplied by outside vendors. Essential Functions: Perform in-process and final inspection activities to ensure all products are manufactured in compliance with work order, traveler, and blueprint specifications. Develop and maintain inspection reports and documentation. Measures all parts according to blueprint using Vernier caliper, micrometer, protractor, height gauge, hole and thread gauge, and other tools as needed. Aids in troubleshooting problems during inspection activities and recommends corrective actions to resolve issues. Follow up on all cases involving product issues and provide resolution recommendations to Quality Manager, Lean Coordinator, Plant Manager, or Engineering Manager Maintain periodic inspection schedules to ensure spot checking of production quality. Maintain 3rd party inspection process. Maintain the returns and reject re-distribution and scrap procedures. Minimum Qualifications 1-4 years of experience in the quality field Experience with blueprints and calibrating measurement tools is required. Good Oral and written communication skills. Understanding of the manufacturing process. The ability to work with minimal supervision. Strong time management skills. Monday-Friday

Quality Inspector III are experienced inspectors who are able to perform more complex manual inspection tasks as well as train other inspectors in proper use of tools and print reading/Geometric Dimensioning and Tolerancing (GD&T). They have a demonstrated proficiency in the use of more advanced tools, such as optical comparators and profilometers. These individuals perform their daily work with minimal supervision and may supervise/guide the work of other inspectors. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Review and verification of supplier-provided paperwork to ensure correctness and completion. Visual inspection of parts, checking for completeness, damage, and foreign objects. Dimensional verification of parts for noted characteristics using both basic hand tools, such as calipers, micrometers, pin gauges, and thread gauges and more advanced tools, such as optical comparators and profilometers. Completion of inspection reports and other required paperwork. Verification of tool calibration prior to use. Acting as an example to the rest of the plant on use of procedures, following rules and policies, and cleanliness. Ability to provide guidance and clarification of work to less-experienced inspectors. SUPERVISORY RESPONSIBILITIES May be asked to provide guidance and direction to other inspectors. QUALIFICATIONS Education and Experience * A high school diploma or GED is the minimum education level for this position. * Three or more years of prior inspection experience is required. * Basic computer skills, particularly Microsoft Excel, is required. * A thorough understanding of print reading and Geometric Dimensioning and Tolerancing (GD&T) is required. * Attention to detail, organization, and a high degree of work ethics are essential. * The ability to provide training and guidance to less-experienced inspectors is required. Language Skills This position requires the ability to read, understand, and draft technical instructions. A thorough understanding of print reading and Geometric Dimensioning and Tolerancing (GD&T) is required. Bilingual in Spanish and English is a plus. Software/Analytical Skills Proficiency with Microsoft Excel is required. Experience with common Microsoft Office Suite applications (Word, Excel, Outlook, Teams) is required. The ability to analyze and interpret defect conditions is essential. Reasoning Ability The ability to make decisions based upon incomplete data is important in this position. PHYSICAL DEMANDS The employee should be able to move items up to 50 lbs. Employee will be required to pass an annual eye examination. WORK ENVIRONMENT The work environment for this position is on our production floor, which includes both areas of climate control and areas that are less controlled. This position may require extended periods of sitting or standing. All Job Posting Locations (Location) Lancaster Remote Type On-Site EEO Statement Boyd Corp is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Temp To Full-Time Perform regular quality assessments on all incoming materials from vendors and outgoing products for shipping. Reject all products and materials that fail to meet quality expectations. Read blueprints, plans, and specifications to understand the requirements of products and services. Measure product dimensions, examine functionality, and compare the final product to the specifications. Recommend improvements to the production process to ensure quality control. Document inspection outcomes by completing detailed reports and performance records. Teach the production team about quality control concerns to improve product excellence. Supervise the production process. Resolve quality-related issues in a timely manner.

SMS Staffing is Hiring - Quality Control Inspectors! Job Title: Quality Control Inspector Job Type: Temp to Hire Pay: Starting at $18/Hr.+ (based on experience) Shift: 2nd Shift | 4:00 PM - 12:30 AM (Monday - Friday) Job Summary We're looking for detail-oriented inspectors to help maintain product quality. As a Quality Control Inspector, you'll check components, in-process materials, and finished goods, keep accurate inspection records, submit samples to the lab, and report defects. You'll also have the authority to place materials on hold or halt production if needed. Key Responsibilities Inspect materials and products against standards Record inspection and test data Submit samples to the lab Report defects to Production, Shipping, and Quality management Place materials on hold or release as appropriate Halt production or shipment if safety or quality issues arise Maintain a clean and safe work area Follow all safety and food safety policies Requirements High school diploma required; training in industrial quality practices preferred Basic math skills Ability to read and follow job orders and specifications Strong attention to detail Ability to work independently Experience with inspection tools like calipers preferred Physical Demands Frequent standing, walking, bending, kneeling, crouching, and reaching Lift/move items 10-50 lbs regularly Visual acuity for close, distance, color, and depth perception Join the SMS team! It takes more than top-notch facilities, modern equipment, and innovative technologies to become our customers' most trusted supplier. It takes people who are committed to our customers' success and who are willing to go the extra mile to get the job done right. #SMS

Ohly is the third largest yeast extract producer in the world with sites in Germany and the USA. We develop, produce and deliver high-quality yeast-based flavours and specialty powders. Ohly is part of the $17.6bn turnover Associated British Food (ABF) Group. ABF is a broad portfolio of businesses which includes Primark, Ovaltine, Twinings, AB Enzymes, and is the world's second largest producer of both sugar and baker's yeast. ABF takes a long-term perspective on investment and performance, and stimulates entrepreneurship by giving high degrees of autonomy to operational businesses. This means that decisions are taken as close as possible to their point of impact allowing teams the freedom to act, in order to be successfully flexible and fast. ABF invests a great deal in selecting and developing the right people for Ohly and the broader ABF group of companies. Ohly has a great opportunity for a Quality Technician to join our team in Boyceville Wisconsin USA. This role ensures that all ingredients, in-process samples, and finished goods meet established product specifications and regulatory standards. You will play a key role in maintaining quality programs, implementing new testing procedures, and supporting continuous improvement initiatives. In this exciting role you will be responsible for: Analytical Lab * Analyze and approve incoming ingredients, in-process samples, and finished goods using established test procedures. * Implement new testing procedures and integrate them into daily operations. * Coordinate inline quality checks with Production Supervisors and the Production Manager. * Contribute to quality programs, including training personnel. * Initiate purchase requests for QC supplies and submit for approval. * Actively pursue cost reduction strategies for testing and supplies. * Conduct physical inventory of hold and rework items. * Maintain up-to-date product, raw material, and manufacturing SOPs. * Coordinate plant water testing, environmental sampling, and sanitation inspections; report results to the Quality Control Manager. * Update and write procedures based on customer specifications. * Review test results and recommend acceptance or rejection of materials and finished goods; report deviations to the Quality Control Manager. * Issue Certificates of Analysis for finished products. * Perform equipment and environmental audits as required. * Complete required reports and documentation to support manufacturing operations. Projects * Facilitate maintenance and repair of QC testing equipment. * Summarize and report on special projects; assist as assigned. Safety * Participate in Ohly Americas safety program, including safety meetings, GMP audits, and safety inspections. * Comply with Good Manufacturing Practices and the Food Safety Plan. * Report food safety issues to authorized personnel. You should have: * Associate Degree in Science, Chemistry, or related field (Bachelor's degree preferred). * Knowledge of HACCP, GMPs, and GLPs. * Proficient in PC applications. * Strong mechanical aptitude. * Excellent written and verbal communication skills. * Strong analytical, organizational, and time management skills. * Knowledge of fermentation, blending, spray drying, roller drying, and packaging preferred. * Experience in regulatory compliance. * Mechanical trade skills are a plus. We look forward to your application including information about your earliest possible start date and salary expectations!

As a valued Trelleborg team member, you will enjoy: Greater opportunity for impact Competitive compensation Generous benefits package: Health, Dental, Vision, STD, LTD, Life, 401k Paid time off Bonuses Pay and Schedule: $19 - $24 per hour Hours: 6:00am - 2:30pm Monday through Friday Qualifications: High School diploma or equivalent Required: 0-3 years' experience in manufacturing environment Desired: Experience with clean room manufacturing Responsibilities: Conducts inspections to ensure compliance with product specifications. Inspections include visual, dimensional, functional, and physical testing on product from all departments. Performs all duties per appropriate work instructions. Completes required documentation. Verifies packaging and documents for shipping parts. Performs accurate data entry. Collaborates and gathers documentation or data, tests product or materials for root cause analysis, investigations, and drives continuous improvement activities. Communicates orally in a professional, courteous manner. Written communications should be clear and concise. Serves as a good team player. Uses Lean Enterprise methods to reduce waste and complexity in all processes and organizes work area. Ensures work area is clean and safe. Assists with filing or scanning for QA Dept. Able to accurately scan processing records to computer files for archiving.

AMPI owns seven Midwest-based manufacturing plants where 10 percent of the nation's American-type cheese, processed cheese and butter is produced. The cooperative's award-winning cheese, butter and powdered dairy products are marketed to foodservice, retail and food ingredient customers. In 2019, the co-op launched its Dinner Bell Creamery brand and accompanying Co-op Crafted promise, highlighting more than 50 years of dairy farm families partnering with skilled buttermakers and cheesemakers. This internship will allow the qualified candidate to participate in a learning program designed around training into a potential full-time opportunity of a role similar to the one in the description listed below. DoD SkillBridge participants are not eligible for compensation from Associated Milk Producers, Inc, as they continue to receive military compensation and benefits as active-duty service members. ESSENTIAL RESPONSIBILITIES This list of duties and responsibilities is not all inclusive and may be expanded to include other duties and responsibilities as management may deem necessary from time to time: All AMPI employees have an obligation to report employee safety, food safety and food quality issues to personnel of authority. This position has a heightened food safety and food quality responsibilities. Execute required tests on finished product according to SOPs and customer requirements. Execute required test on incoming ingredients according to QMS (Quality Monitoring Scheme). Responsible for daily/weekly plating, reading, calibration, sample collection, Internal Control Plan, sample preparations, etc. Support investigations on improvement projects (e.g., holds, consumer complaints), helps to identify root causes, and helps to identify corrective actions and monitors for effectiveness. Support training for operators to ensure process checks are accurate and timely as state in QMS. Communicate out-of-specification product results to supervisor. Calibrate lab equipment such as pH meter and scales, etc. according to SOP's. Conduct daily routine sample analyses using lab techniques and other instrumentation following Good Laboratory Practices (GLP). Organize laboratory records and files. Ensures compliance to procedures and work instructions. Ensures correct recording of laboratory and quality records in compliance with SOP's including storage and retrieval of records. Support laboratory activities to ensure that a high quality of products, services, housekeeping, and hygiene standards are maintained and improved in laboratory and other analytical areas. Supports laboratory compliance (calibration, equipment testing, etc.) to SQF and AMPI requirements. Employee shall follow and carry out company policy on all required GMP, quality and food safety requirements and escalate quality or food safety findings or incidents. Support execution of GMP's throughout the plant and follow safety rules and procedures. Support improvement of GMP's throughout the plant and follow safety rules and procedures. Support improvement initiatives (e.g., complaints, holds) for facility. Other duties as assigned.