Quality inspector jobs in Maple Grove, MN

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

Kurita America is part of the Kurita Group, one of the leading water solutions providers in the world. Established in 1949, the Kurita Group is comprised of an international network of approximately 8000 employees located in 18 countries. Located in Minneapolis, MN, Kurita America brings innovations to market through a holistic water management approach, incorporating state-of-the art equipment, chemistries, engineering, and services to conserve natural resources for a better, more sustainable world. Kurita's corporate philosophy is to study the properties of water, master them and create an environment in which nature and humanity are in harmony We have an immediate need for a Quality Inspector in our Brooklyn Park facility. Title: Quality Inspector Location: Brooklyn Park MN Compensation: $35 to $40/hr Responsibilities Conduct visual inspections of welds to ensure compliance with industry standards and specifications Review welding procedures and specifications to ensure compliance with industry standards and customer requirements Provide guidance and support to welding personnel to ensure that welding activities are performed in accordance with industry standards and specifications Prepare inspection reports and maintain accurate records of all welding activities and submit them to the manager. Collaborate with other departments to ensure that welding activities are integrated into the overall project plan Inspection of fabricated vessels and skidded systems Installation of internal vessel components and assemblies Submits inspection, photos, and other reports as required for each inspection Maintain good working relationships with supplier quality control personnel In-house inspection of fabricated parts In-house fabrication of PVC internal vessel components and assemblies Review welding procedures and specifications to ensure compliance with industry standards and customer requirement Provide guidance and support to welding personnel to ensure that welding activities are performed in accordance with industry standards and specifications Qualifications Education: Diploma from trade school, preferably in welding. Experience: 3 - 5 years working in a manufacturing environment Experience of inspection of PVDF/PP piping welding for high purity (Semiconductor project) application. Experience in inspection of PVC piping/bonding. Knowledge of Welding procedure specification (WPS), Welder qualification test record (WQTR), Procedure qualification record (PQR). Proficient with MS-Office Products including Excel and Teams Able to read and interpret engineering drawings. Familiar with mechanical measuring equipment and tools. Knowledge, Skills and Abilities: Excellent knowledge of ASME B31.3, Must have knowledge of ASTM, ASME and D1.1.National association of corrosion engineers (NACE), good knowledge of computer skills. EEO/AA/F/M/Vet/Disabled

Responsibilities: Supervise and audit truck loading/unloading of 20-40 wooden book carts per truck. Verify compliance with Google's packing/handling instructions at pickup library sites. Observe loading process, document compliance, take photos, and prepare full report. Ensure professional representation of ProQC and CLIENT on-site. Recurring 1-2 inspections monthly at assigned location. Technical & Industry Experience: Minimum 3- 5 years in quality inspection, container loading supervision, or field audits. Strong understanding of container loading supervision and packing audits. Familiarity with auditing bulk/specialized cargo handling (wooden carts, books, or equivalent). Ability to verify compliance against written packing/handling instructions. Strong reporting and documentation skills. Logistics, warehousing, shipping, or field audit inspections. Experience with corporate clients, libraries, or academic institutions an added plus. Job Type: 1099 Contractor Project Duration: Monthly recurring inspections through approx. March-June 2026. Note: This is a 1099 contract role - project duration may vary based on client needs Shift Hours: Typically, during library pickup hours (daytime, exact times TBC with logistics partner).1 inspector per city per assignment. Note: As a 1099 contractor, project schedules may vary depending on site availability Location: Must be able to travel to Minneapolis, MN and nearby areas (exact CLIENT address can ONLY be shared once contractor joins) Compensation: $22.00 - $32.00 per hour About Us Since 1984, Pro QC International goes above and beyond the traditional roles of quality control. We assist clients to put better quality products on the market by resolving quality and production related challenges and reducing supply chain risk and cost. Pro QC offers solutions in over 88 countries. We manage our global operations from 18 Offices Worldwide. Our clients range from small start-ups to multinational companies in the Americas, Europe, Asia, the Middle East and Africa. Join Our Team We are always looking for talented candidates in Asia, Americas, Europe, Middle-East, and Africa. At Pro QC, we value quality over quantity. We value professionalism, dependability, and teamwork. We believe in building trusted partnerships that are earned through conscious efforts. In our strive for excellence, we are passionate about delivering quality solutions to organizations around the world. Leveraging an ever-expanding, interconnected group of people from diverse backgrounds, Pro QC offers an attractive and unique opportunity as part of a global family. Our Vision: To nurture the trust of our customers and our team through dynamic interactions, creative supply chain solutions, and integrated partnership.

The Quality Inspector II performs basic audit, inspection, test, and measurement duties on standard products and processes to ensure conformance to requirements. Essential Functions Performs basic visual and mechanical inspection of product and components per documented procedures; specification; drawings; or generally accepted good manufacturing practices, using measuring equipment (i.e., caliper, micrometer, ruler, measuring scope, and laser micrometer) Responsible for controlling, monitoring, and quarantining of non-conformant product and materials Understands the requirements of the Quality System such as best documentation practices, quality standards, and basic ISO requirements Acquires or provides training as needed Responsible for receiving inspections and in-process inspections Support company finance, accounting, human resources, quality, regulatory, and clinical departments as necessary to ensure compliance with requirements Requirements Education, Experience, Required Skills 3-5 years of quality experience, including basic blueprint reading and basic understanding of GD&T principals Reliable, motivated self-starter with an aptitude for development Working knowledge of inspection techniques and instruments, quality control terminology and competency in the use of ISO 13485 Standard Proficient in Microsoft Office Word & Excel Ability to define problems, collect data, establish facts, and draw valid conclusions Flexible and able to handle multiple projects in an organized, timely manner Ability to problem-solve, work under pressure, and to effectively manage stress Physical Requirements Prolonged periods sitting at a desk and working on a computer. Ability to sit, stand, lift, bend and stoop numerous times throughout the day. Must be able to lift 25 pounds at times. Must have manual dexterity. Must have excellent hand-eye coordination. Must wear gown, gloves, and ear protection if applicable. Summary of Benefits Company-paid benefits: Employee Life Insurance & Accidental Death & Dismemberment (AD&D), Long Term Disability (LTD), Kavira (requires participation in medical plan). Voluntary, employee-paid benefits: Employee Supplemental Life & AD&D, Spouse and Dependent Life & AD&D, Short Term Disability (STD), Accident, Critical Illness, and Hospital Indemnity, Employee Assistance Program. Accrued Paid Time Off (PTO) & Floating Holidays Paid Parental Leave Paid Holidays Benefits and incentive compensation may be subject to generally applicable eligibility, waiting period, contribution, and other requirements and conditions. Compensation The typical base pay range for this role is between $25.00-31.00/hour. Compensation may vary based on individual job-related knowledge, skills, expertise, and experience. This position is eligible for a discretionary annual incentive program driven by organization and individual performance. Company-provided Safe Harbor Contribution of 3% of eligible earnings.

Company Overview: Biomerics is a world-class manufacturer and innovative polymer solutions provider for the medical device and biotech industries. As a vertically integrated company, we specialize in the design, development, and production of medical devices for diagnostic and interventional procedures. We are focused on next-generation solutions for the vascular access, electrophysiology, cardiac rhythm management, neurovascular, structural heart, and cardiovascular markets. At Biomerics, we are dedicated to our diverse employee base. We understand that a strong, skilled, and engaged workforce is the foundation of our continued success as a business. We strive to live up to the Biomerics values in all our interactions. It is an exciting time to be part of our collective team. There is no limit to the impact that can be achieved here at Biomerics. We improve and advance our employees' lives, and the lives of the patients that depend on our products. At Biomerics we believe in integrity, partnership, empowerment & accountability, trust, agility, teamwork, excellence, and we care. Our team-oriented, customer-focused corporate culture places a premium on building strategic, mutually beneficial partnerships with customers as well as our team members. Biomerics is a leading provider of laser processing services and contract manufacturing of medical components and assemblies to a wide range of customers throughout the United States and internationally. The company develops and implements leading-edge part-specific manufacturing processes utilizing such high-tech manufacturing tools as rapid prototyping, automation, PLCs, robotics, and vision systems. The company offers a uniquely friendly and supportive environment and strongly encourages its employees to learn and grow in their careers. The company offers its eligible employees a range of benefits which include medical and dental benefits, 401K, and paid time off. JOB RESPONSIBILITIES: · Quality product support including; but not limited to; Receiving Inspection and verification, Final Product Inspection and Batch Release certifications, Internal Audits, Quality Documentation and Records activities. · Support the management team and production associates to ensure established product/component requirements are met. · Provide component and material inspections and final product inspections in a timely manner to ensure Production and R&D schedules are met. · Being a liaison between Operations and Quality departments. · Support the Internal Audit Team to perform scheduled audits. Requirements Requirements · College or Technical College education preferred · Minimum 5-yrs experience in the medical device manufacturing environment preferred · Competent experience with MS-Office (Word, Excel, Power Point, etc.) · Competency with handheld dimensional inspection equipment and Automated Test Equipment · Competency with Geometric Dimensioning and Tolerancing · Experience performing/programming inspections with a CMM preferred · Experience in performing open dimensional inspection setups a plus · Must be able to follow written instructions and procedures · Must possess good organizational skills · Must show initiative taking on and completing projects including other assignments as requested ·Must possess good verbal and written communication skills · GD&T knowledge preferred · Zeiss Machine knowledge preferred

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 *********************

NOW HIRING: Millerbernd Manufacturing is looking for a Circular Products Quality Inspector 2 to join our weekend shift team. The Circular Products Quality Inspector 2 is responsible for the testing and inspection of products at various stages of production process in compliance with applicable codes and standards. Supporting first inspection through final inspection for all OEM products. Job Title: Circular Products Quality Inspector 2 Location: Winsted, MN Salary Range: $22.95 - 27.00 per hour (In compliance with Minnesota Pay Transparency Law, this range reflects the anticipated compensation for this role. Actual pay may vary based on experience, education, and other factors.) Shift Schedule: Weekend shift Friday - Sunday 5am - 5pm Shift Differential: Weekend shift - $2.50/hour As a Circular Products Quality Inspector 2, you will: Perform repetitive inspection following standard methods and procedures Visually inspect product using a variety of precision measuring instruments Check dimensions and finishes against blueprint or work order specifications Mark test parts with appropriate language per job specifications Initiate accept/reject decisions and know when to call more qualified individuals for marginal evaluations Contain defective material at source Keep accurate inspection records Inspect and calibrate test equipment; document dates and results Write formal inspection reports Lead problem solving activities to determine root cause Assist with production as required Assist with root cause investigation of material defects or other problem-solving activities Read blueprints Participate and support Continuous Improvement initiatives Maintains 5S guidelines Communicate relevant information and concerns positively and effectively to others in timely manner Perform work at the appropriate pace to maintain quality and productivity requirements Enter job data in production tracking system Role Qualifications as a Circular Products Quality Inspector 2: Preferred candidates will have background knowledge in inspection, be able to read a tape measure and blueprints, and use basic hand tools as well as a caliper and micrometer Other combinations of formal training and experience may be considered Knowledge of industry specifications (AWS, ASTM-123, DOT, etc) Knowledge of problem-solving activities and ability to apply those engineering/lean concepts Computer literate; particularly in word processing, spreadsheet, email, and shop floor control, applications Ability to read and understand required internal manufacturing paperwork Effective and appropriate oral communication skills including legible handwriting in English Able to work under limited supervision using standardized practices and/or procedures Ability to electronically record production information Why Millerbernd and Who We Are: We strive to create the best opportunities for our employees. Here you can discover your potential, turn your ideas into reality and become a part of a team with skills and experience in various disciplines. At Millerbernd, you will enjoy a fulfilling and dynamic work environment, exclusive professional development opportunities, exceptional benefits, and competitive compensation. Comprehensive Benefits Package At Millerbernd Manufacturing Company, we offer a benefits package designed to support your health, well-being, and financial security. Health & Wellness Medical Insurance: Choose from two high-quality plans, including PPO and High Deductible options, with company contributions to HSAs Prescription Drug, Dental, and Vision Coverage Health Savings Account (HSA) and Flexible Spending Accounts (FSA) for medical and dependent care expenses Income Protection Employer-paid Basic Life and AD&D Insurance Short-Term and Long-Term Disability Insurance at no cost to employees Voluntary Benefits Optional Life and AD&D Insurance, Legal and Identity Protection, Accident Insurance, and Critical Illness Insurance Retirement Savings 401(k) Plan: Employer matching contributions up to 4%, with immediate vesting Incentive-Based Compensation Eligible employees are included in one of our incentive programs, designed to reward performance and align with company profitability and goals. Incentive program eligibility and payout specifics are determined by the role and shift schedule. Work-Life Balance and Additional Benefits Paid Time Off (PTO) and Paid Holidays Tuition Reimbursement: Up to $5,250 annually for job-related education Employee Assistance Program (EAP): Free and confidential support services Onsite Training Programs: Skill-building opportunities, including leadership development, welding classes, and language courses Uniform Subsidy for applicable role Eligibility: Benefits are available to employees working 30+ hours per week. The 401(k) plan is available to all employees, regardless of hours worked. Equal Opportunity Employer Statement Millerbernd Manufacturing Company is an equal opportunity employer committed to fostering an inclusive environment. We encourage candidates from all backgrounds to apply. Note: We are unable to sponsor employment visas at this time. The Process: After you've submitted your application, here is what you can expect to happen next: Your application will be reviewed by our internal Talent Acquisition Team, not a robot or computer software program. Once our team has reviewed your application and your skills, qualifications, and experience match what we are looking for, we will reach out to set up a phone interview. After we've had a chance to chat with you, we will pass your application and our notes on to the hiring manager. From here, the hiring manager will review the information and determine next steps. Next steps would include an on-site interview and tour of the facility to see what you could be doing here at Millerbernd Manufacturing. From here, the hiring manager would discuss the interview with the Team Lead (if applicable) and determine to move forward or not. Throughout the process, you will receive communication from our Talent Acquisition Team regarding the status of your application and the next steps if applicable. On average, our hiring process takes 3-10 business days once your application is submitted. Apply Now if this sounds like you!

Advanced Volumetric Alliance (AVA) is a volumetric off-site building manufacturer that creates entire buildings in a factory environment. Our culture requires brilliant executers who thrive in a fast-paced and innovative team. AVA designs, engineers and manufactures industry-leading full volumetric modular units for the multi-family apartment and hospitality industries in a 180,000ft2 state of the art facility in Albertville, Minnesota. Job Description: The Quality Inspector role is instrumental in ensuring that AVA meets not only the quality expectations of our customers, but also the State and local authorities as well. This motivated individual will help establish systems and processes that ensure conformance to company quality standards, specifications, and applicable building codes, while maintaining a respectful but firm relationship with team members within production. Responsibilities: Develop a comprehensive working knowledge of functional documentation. This includes ensuring the constructed modules meet specifications, applicable codes, production drawings and technical details. Work with the Quality Supervisor on projects for technical document writing, data analytics, root cause determination and corrective action implementations. Participate in pre-build, post-build and active manufacturing design reviews by providing crucial QC feedback to the designers. Perform inspections by utilizing Inspection Checklists. Conduct examinations, witness testing of systems, sub-systems and components. Document and report results. Support cross-functional efforts to improve the condition of the finished product and ensure quality is built into the process to reduce waste such as rework. Conduct investigations and use problem solving skills to drive continuous improvement initiatives like 5S, internal audits, Inspection Sheet updates, new project development and more. Communicate feedback and preventative actions to production personnel on a regular basis, along with reporting of KPIs (Key Performance Indicators) when available. Support the Receiving group by sorting and handling defective materials and generate NCMRs in relation to said nonconformances. Learn and grow within an organization that provides continuous education opportunities to be implemented immediately at AVA, but also to stay with an individual as their career blossoms. Perform other related duties as assigned by the Quality Supervisor and/or Vice President of Construction.

Brooklyn Park, MN | Direct Hire | $45-$55/hour We're seeking a skilled and detail-oriented Quality Inspector to support manufacturing operations in Brooklyn Park. This contract role focuses on inspecting welded and fabricated components to ensure compliance with customer specifications, industry codes, and internal quality standards. The ideal candidate will have strong mechanical aptitude, hands-on inspection experience in a manufacturing environment, and certification as an AWS Certified Welding Inspector (CWI). Responsibilities Perform visual inspections of welds and fabricated components to verify compliance with drawings, specifications, and standards. Review welding procedures (WPS), qualification records (PQR, WQTR), and related documentation for adherence to project and industry requirements. Provide technical guidance to welding and fabrication personnel to ensure proper techniques and quality practices are followed. Conduct inspections of fabricated vessels, skidded systems, and internal vessel components. Support in-house fabrication and inspection of PVC, PVDF, and PP components. Prepare and maintain detailed inspection reports, photos, and records for all quality activities. Collaborate with engineering, production, and quality departments to integrate inspection activities into project schedules. Qualifications Diploma or certification from a trade school, preferably in welding or a related discipline. 5-7 years of experience in a manufacturing or fabrication environment. Hands-on experience inspecting PVDF/PP piping welds for high-purity or semiconductor applications. Experience in inspecting PVC piping bonds and related assemblies. AWS Certified Welding Inspector (CWI) required. Familiarity with WPS, WQTR, and PQR documentation. Certified in Non-Destructive Testing (NDT) methods. Strong working knowledge of ASME B31.3, ASTM, ASME, and AWS D1.1 codes. Understanding of NACE (National Association of Corrosion Engineers) standards preferred. Be the first to learn about future positions by joining our Newsletter and following us on LinkedIn! Konik is an equal-opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as a qualified individual with a disability, or any other protected class status. Konik has been a leader in the technical staffing industry for more than 50 years, providing the fastest and easiest link between employees and employers. Konik has specialized in placing professional, qualified personnel in Minnesota and western Wisconsin businesses since its inception and maintains a strong commitment to customer service.

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.

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.

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

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: Monitor and verify quality in accordance with specifications, statistical process or other control procedures. Perform work involving measurement and physical quality comparison to predefined dimensions and specifications. Essential Job Duties and Responsibilities: Perform visual and dimensional inspections of received, in-process, and finished components, subassemblies, and products. Aide in completing inspection of product per predefined methods, to verify product quality meets customer specifications required. Provide information regarding product quality and conformance to specification to manufacturing team. Assist Quality, Engineering and Production teams in investigations of process related quality issues. Work with production to resolve Quality issues and verify documentation is complete. Maintain required information systems regarding quality, inspection reports, equipment maintenance, calibration logs and non-conforming material reports. Assist in completion of GR&R studies, capability studies and other inspection reports, employee evaluations and review process. Other duties as assigned. Essential Qualifications: High School Diploma or equivalent and 2 years of experience in the plastics industry, clean room / medical device assembly. Knowledge and practical understanding of various assembly Inspection methods and inspection equipment. Proficient with Microsoft Word and Excel. Desirable Qualifications: ASQC certification preferred. Experience with inspection equipment such as CMM, Vision System, and common dimensional inspection hand tools. Working knowledge of ISO, FDA, GMP, and OSHA standards. 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 to30lbs. 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 Weekday 2nd shift, Monday through Friday 2:00PM-10:30PM.

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

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.

**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: $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.

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.