Quality control inspector jobs in West Saint Paul, MN

**Department:** Engineering, Industrial & Quality **Electric Machinery Company, a division of WEG Electric Corp.** **Minneapolis, MN** ** **Quality Inspector / Electrical Manufacturing - 1st Shift** Department: Quality Team Department **Primary Objective of Position** 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:** 1. Inspect parts or products using appropriate instruments, following pre-established standards and procedures, and guide other inspectors in their activities. 2. Conduct nondestructive tests, including visual inspection, liquid penetrant testing, magnetic particle testing, and ultrasonic testing. 3. Interpret specifications relevant to your area of activity, such as standards, product drawings, electromechanical specifications, and catalogs. 4. Compare inspection results with specification values, making decisions on acceptance or rejection based on conformity. 5. Perform inspections on special products, monitor them, and address any issues that arise. 6. Analyze customer purchase orders, drawings, specifications, standards, and modifications to ensure product conformity and verify quality assurance conditions. 7. Coordinate with support areas (e.g., Sales, Product Engineering, PCP, Purchasing) to assess product and material conformity. 8. Identify inspected items with appropriate labels and inform the production area leader if necessary. 9. Prepare inspection reports detailing the quality of parts, finished products, or in-process items, highlighting relevant findings. 10. Calibrate measuring instruments and devices using reference standards for various inspections. 11. Maintain data on quality issues related to non-conformance. 12. Commit to Continuous Improvement by identifying and acting on opportunities in daily work. 13. 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**

Job DescriptionSalary: $26 - $31 /hr + 10% 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.

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

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.

TAK Broadband is a leading end-to-end U.S. fiber broadband network construction contractor operating in 42 states. It builds more than just networks; it connects communities to new valuable digital opportunities. TAK offers comprehensive service solutions, from construction to drops to fulfillment. TAK's ecosystem of partners allows it to successfully complete every project starting from the first point of conception. This includes engineering teams, distributors, and more than 100 qualified construction crews with extensive experience across all ISP types and markets; over 300 experienced bury drop crews; and more than 700 professional technicians. We are seeking a Quality Control Technician to join our team in the Minneapolis, MN area. In this role you will ensure timeliness, completeness and accuracy of work performed by technicians. You will perform inspections post-install to ensure compliance to client specifications and complete reviews to ensure proper restoration of the area. Why TAK? * Full Time * Paid Weekly * Compensation: $20 - $22 per hour, DOE * Full Benefits Package (Medical, Dental & Vision) * Paid Time Off * 401(k) with Company Match! * 25K Company Paid Life Insurance * Independent Work & Team Collaboration * Career Development & Advancement Opportunities! The Role * Ensures timeliness, completeness and accuracy of work performed by technicians * Performs inspections post install to ensure compliance to client specifications * Completes reviews to ensure proper restoration of area * Captures photos and attach to the inspection report * Performs white line excavations and collects locate data * Verifies the system is complying with all safety requirements * Performs work in a safe manner, following all OSHA and company guidelines * Prioritizes, organizes and efficiently completes tasks to meet deadlines * Works in a variety of outdoor environments * Drives Company vehicles responsibly and safely * Conducts and attends meetings as needed Requirements * 2+ years of telecommunications (i.e. cable, internet, telephone, wireless) installation or construction industry experience (sales, call center and IT roles are not considered) * Experience with quality control and verifications * Experience calling in Bluestakes a plus * Experience with underground locates and the ability to use a compass for directional instructions * Basic mechanical aptitude, ability to utilize hand tools for intended purposes * Ability to travel daily around the Chicago metro area and open to a variety of schedules * Excellent customer service, time management, problem-solving and troubleshooting skills * Ability to learn and operate testing equipment and software/programs * Ability to utilize hand tools, identify wire size/color and accurately utilize measuring devices * Ability to carry, climb, operate, and work upon an extension ladder (approximately 28 feet high and 75 pounds) * Ability to complete work indoors, outdoors, in tight spaces and elevated by bending, reaching, twisting, climbing, and working while standing up to 70% of the time * Ability to safely navigate various terrains, managing equipment and tools * A body weight of no more than 275 pounds to perform ladder work safely. Safety is our #1 Priority. If personal safety is not compromised, an accommodation may be available based on previous ladder experience in a similar role * Valid driver's license with a satisfactory driving record (no suspensions or revocations) * Passing of all pre-employment requirements (MVR, Background Check, Drug Screen) The compensation and benefits information is accurate as of the date of this posting. The Company reserves the right to modify this information at any time, with or without notice, subject to applicable law. TAK is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by law. We maintain full compliance with the Americans with Disabilities Act and are committed to providing equal access throughout our employment practices. Individuals with disabilities may request reasonable accommodations during the application and hiring process by contacting *****************************. Salary Description $20 - $22 per hour, DOE

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: * 3rd shift: 10:00pm-6:30 am Sun-Thurs Responsibilities * Inspection of received materials, components, and assemblies relating to quality, appearance, and performance * Interpret and accurately document the results of the inspections and testing * Report and isolate non-conforming product * Use a variety of inspection measurement tools and gages (Micrometer, Caliper, Gage Pins, Indicators, Thread Gages, Profilometer, Optical Comparator, Microscopes) * Operate various precision testing equipment including but not limited to Tool Scope, CMM, and Vision systems * Support and comply with the company Quality System, ISO, and medical device requirements * Read, understand, and follow work instructions and standard work * Partner with other business segments: sales/marketing, customer service, engineering, quality, and finance * Understand customer needs and the core business markets we serve * Ensure business systems are implemented, maintained, and functioning properly * Participate in required company meetings * Maintain an organized work area (5S) * Participate in the Operational Excellence Program * Complete all other work duties as assigned * Ability to work in a manufacturing environment 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 *********************

The Quality Inspector is responsible for general and specific quality control functions related to the inspection of OEM-distributed components. This role ensures products meet defined standards, specifications, and customer requirements. Key responsibilities include inspecting, analyzing, interpreting, reporting, and ensuring quality assurance in alignment with ISO 9001 and AS9120 requirements. The Quality Inspector plays a critical role in delivering compliant products to customers in a timely and accurate manner. ESSENTIAL DUTIES AND RESPONSIBILITIES * Perform detailed inspections of incoming, in-process, and outgoing products using mechanical tools such as calipers, micrometers, thread gauges, and height gauges * Evaluate product against engineering drawings, specifications, and quality standards to ensure conformance and fitness for use * Accurately document inspection results, findings, and disposition decisions using internal quality systems, ensuring traceability and compliance with ISO 9001 and AS9120 standards * Analyze data and inspection results to detect trends, recurring issues, or potential risks to product quality * Interpret quality standards and specifications to make informed decisions on acceptability and escalate issues when necessary * Generate non-conformance reports (NCRs), assist with root cause analysis, and support the development of corrective and preventive actions * Assist in internal audits, supplier evaluations, and quality system reviews * Collaborate with cross-functional departments to ensure timely resolution of quality concerns and support continuous improvement initiatives * Ensure all inspection tools are calibrated and properly maintained * Maintain a clean, organized, and safe inspection area that supports efficient and accurate work EDUCATION, QUALIFICATIONS, SKILLS & ABILITIES * High school diploma or equivalent required; technical or trade school training preferred * Minimum of 2 years of experience in a quality inspection or control role, preferably in an OEM distribution or industrial setting * Familiarity with ISO 9001 and AS9120 quality systems and documentation * Strong understanding of quality assurance principles and statistical sampling methods * Skilled in using precision measuring instruments and interpreting technical drawings and specifications * Ability to analyze and report inspection data accurately and consistently * Excellent attention to detail, communication, and organizational skills * Proficient with Microsoft Office and ERP/QMS systems for data entry and recordkeeping The Würth Difference: * Proactive supply chain solutions customized to your business, your industry * Industrial products and services delivered with prompt, personal attention * Inventory management solutions that keep your production line moving smoothly * Complete program support from initial design, to implementation, training, to ongoing analysis Why Würth: * Maternity/Paternal leave after 1 year of service * Tuition Reimbursement eligible after 1 year of service * Health benefits and programs - medical, vision, dental, life insurance and more * Additional benefits 401(k), short term disability, long term disability * Paid Time Off, accrued per pay period, additional day earned per year of service * 10 paid holidays EEOC STATEMENT: The Wurth Industry North America group of companies are Equal Opportunity Employers and do not discriminate on the basis of an individual's sex, age, race, color, creed, national origin, alienage, religion, marital status, pregnancy, sexual orientation or affectional preference, genetic trait or predisposition, carrier status, citizenship, veteran or military status, and other personal characteristics protected by law. All applications will receive consideration for employment without regard to legally protected characteristics. Wurth will consider qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state, and local laws.

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

About Us: SMC Ltd. is a globally recognized premium supplier to the medical market with locations throughout the world. People committed to speed, technology, and exceptional performance are the cornerstone of our organization. Comprised of dedicated people and decades of manufacturing experience, we have continued to experience strong growth and currently have outstanding career opportunities for equally dedicated people. Job Summary: Perform routine visual and dimensional inspections of received, in-process, and finished components, subassemblies, and device products to pre-defined dimensions and specifications. Monitor and verify inspection data in accordance with specifications, statistical process, or other control procedures. Provide effective communication regarding product quality status to manufacturing teams. Regular attendance with occasional overtime and other duties as assigned. Essential Job Duties and Responsibilities: Pharma • Perform incoming receiving inspection of pharmaceutical products ensuring accuracy of paperwork and physical sampling. • Perform in-process and product testing inspections with attention to critical accuracy of data entry through either manual or direct data import actions.• Initiate MRB's, properly contain product for any nonconformances.• Perform accurate review and closure of BHR & DHR's, including yield, reconciliation, and OOS. • Responsible for verifications of rework activities independently. • Problem solves inspection equipment and program issues for inaccuracies or poor performance. Essential Qualifications: • Experience in Pharmaceutical Device manufacturing / drug handling• Class 7/ISO 10,000 Cleanroom experience • Critical attention to detail. • Demonstrate strong decision-making abilities. • Proficient knowledge of Good Documentation and Good Manufacturing Practices. • Proficient use of the ERP system. ADA Requirements: • Stand, walk, bend, squat, twist, reach or otherwise move frequently.• Occasional repetitive motion and grasping• Occasional climbing to reach areas on machines or racks.• Lift, move or otherwise transfer up to 30lbs. occasionally, >20.frequently• Typically sits, grasps items, or performs keyboarding for occasional operation of a computer.• Exposure to typical machine shop physical hazards which may require respiratory protection. What SMC has to offer? Clean, Climate-Controlled Environment Stable schedule Paid holiday and PTO Health, dental, and vision insurance 401(k) retirement savings Life and disability insurance Promotional opportunities Training and career growth programs Amazing co-workers Tuition reimbursement Employee Assistance Program At SMC Ltd. we recognize that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. We know that our differences often can bring about innovation, excellence and meaningful work-therefore, people from all backgrounds are encouraged to apply to our positions. Please let us know if you require reasonable accommodations during the interview process. SMC Ltd. is an equal opportunity employer. M/F/D/V; this organization uses E-Verify. Applicants may be subject to pre-employment screening which may include drug screening, reference checks, employment verifications, background screening and/or skills assessments. #IND #LI-HN1 1st shift, 6:00AM - 2:30PM Monday through Friday.

GENERAL DESCRIPTION The Quality Control Technician I is responsible for inspecting and testing our products to ensure conformance with PCI standards and design specifications that are detailed on the pour sheet. This position is critical to ensuring the quality and safety of our products. Salary range ($25.00-27.00). Based on experience. WHY WORK FOR US? At Wells, we empower our team members to deliver an exceptional client experience. Our employees are talented problem solvers that shine in preconstruction, engineering, operations, and project management. They bring innovative solutions that yield outstanding results. In the design and construction industry, we focus on honesty and hard work to build trust that lasts beyond individual projects. Our team is consistently working to improve building processes and raise industry standards. We meet our partners' needs through collaborative efforts that ensure safe and certain results, reducing risks along the way. Together, we help businesses and individuals succeed and change our communities for the better. WHAT WE HAVE TO OFFER Wells values our employees and is committed to providing a competitive and comprehensive benefits package. Please note that the benefits listed here are for non-union employees. Benefits for union employees are covered under separate collective bargaining agreements which can be obtained through their union business agent or their HR representative. Health, dental and vision insurance Paid premiums for short- and long-term disability, and life insurance Wellness Incentives Paid holidays Flex spending for medical and daycare Health savings account (HSA) 401(k) plan with profit sharing Access to Nice Healthcare Employee Assistance Program Paid Time Off (PTO) Wishbone Pet Insurance Critical Illness Benefit Plan Accident Insurance Plan Voluntary Hospital Indemnity Plan Other benefits include Health and Family Care leave for both union and non-union employees. ESSENTIAL FUNCTIONS AND RESPONSIBILITIES Performs pre-pour inspections including dimensions of member, position of reinforcement, location of tensioning strand, and quality of forming. Post-pour inspection of cast product Perform wet and hardened required testing on the materials used in the manufacturing of product. Prepares concrete specimens for testing. Regularly performs test for slump, temperature, unit weight, air content, and cylinder strength. Involved with tensioning of cable to record elongations and ensure cable is tensioned as designed. Perform cylinder strength tests to ensure they meet intended strength. Conduct aggregate gradations and sieve analysis. Compliance with safety policy and procedures. Maintains complete Quality Control documentation for inspections and testing performed. Identify and record quality issues and works with Production to resolve those issues. Acts in professional manner that demonstrates the individual has good character and can be trusted by all employees. Complete special projects as requested and performs other duties as assigned. Willingness to work outside all year long (Location Specific) EDUCATION, SKILLS, AND ABILITIES REQUIRED High School Diploma or GED. Must have interpersonal communication skills to interact with co-workers, supervisors, and managers. Experience with Microsoft Office. Must be able to solve problems quickly and efficiently. General math skills, be able to read a tape measure. Strong attention to detail and organizational skills. Knowledge of safety procedures that need to be followed. Ability to work with others to get the project completed efficiently. Must be motivated and self driven to complete a task. Understand and accepts changes that are implemented to become best in Class. PHYSICAL REQUIREMENTS/ ADA ESSENTIAL FUNCTIONS Physically able to lift up to 75 lbs, occasionally. Physically able to push, pull, lift, bend, climb, kneel, twist, squat, crawl and use hands/forearms repetitively and frequently. Ability to move around for up to 12 hours per day. Ability to work from ladders, scaffolding, swing stages and man lifts at various heights frequently. WORKING CONDITIONS Moderate to high risk of exposure to unusual elements. Moderate to high risk of safety precautions. Moderate to high exposure to production environment. Wet, hot, humid, and wintry conditions (weather related) (plant specific) Ability to work outside year-round (plant specific) This position profile identifies the key responsibilities and expectations for performance. It cannot encompass all specific job tasks that an employee may be required to perform. Employees are required to follow any other job-related instructions and perform job-related duties as may be reasonably assigned by his/her supervisor. Equal Opportunity Employer, including Veterans and Individuals with Disabilities . Wells participates in E-Verify and will provide the federal government with your I-9 Form information to confirm you are authorized to work in the U.S. #INDLABOR

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.

Quality Inspector - Electrical/Manufacturing 1st Shift Department: Engineering, Industrial & Quality Location: Minneapolis, MN START YOUR APPLICATION Electric Machinery Company, a division of WEG Electric Corp. Minneapolis, MN Quality Inspector / Electrical Manufacturing - 1st Shift Department: Quality Team Department Primary Objective of Position 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 START YOUR APPLICATION

Job DescriptionSalary: $22 - $28 /hr + 10% 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.

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 required * 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 *********************

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!*********************

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

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.

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 required 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 *********************