Quality assurance technician jobs in Sterling Heights, MI

contract( 6-12 months) with possible extension Pay Rate $26/hr on w2 with Benefits Working schedule - 2-2-3 working structure - (2 days on, 2 days off, 3 days on, 2 days off) Requirements: Associate degree or higher from an accredited college or university with a major in chemistry, engineering, or related science Valid Michigan Driver's License Responsibilities: Collect field samples of wastewater, sludge, polymer, etc. from various process areas of the Plant and the outfall, and perform chemical, microbiological, toxicological, and physical analyses that include reagent and media preparation, instrument operation, calibration, maintenance checks, and quality assurance/quality control (QA/QC) Become knowledgeable in laboratory analyses and treatment processes. Become proficient in training new hires in process analyses and sampling. Contribute to the record-keeping and reporting of laboratory data, regulatory reporting, operations reports, plant meetings, etc. Validate accurate readings from monitoring equipment, maintain analyzers and perform analyzer reagent change/replenishment. Work Night and Day shifts as assigned. Work in an industrial setting supporting 24-hour operations. Support a large team where needed with a high degree of flexibility. Precisely and diligently follow complex procedures and guidelines. Work overtime if needed to achieve compliance and support operations. Communicate frequently with team members and other units across the organization about the process, equipment, or potential problems. Physical Requirements: This position requires the ability to climb, bend, twist, carry, stack, push, pull and other efforts requiring considerable physical strength. This position also requires the ability to lift a minimum of fifty (50) pounds, walk, stand, or work for long periods of time, demonstrate normal color perception, hear audible alarms, detect abnormal equipment sounds, visually inspect equipment and processes at any time of the day or night.

Job Title: Quality Inspector Technician Job Summary:The Quality Inspector Technician is responsible for ensuring that products and processes meet defined quality standards. This role involves inspecting, testing, and measuring materials and products, identifying defects or deviations, and working closely with production and engineering teams to ensure continuous improvement and compliance with company and regulatory standards. Key Responsibilities: Perform inspections of incoming materials, in-process components Finished products using measuring tools and visual checks Interpret engineering drawings, blueprints, and technical documents to verify product conformance Use tools such as calipers, micrometers, gauges, and CMM (Coordinate Measuring Machine) Document inspection results and maintain accurate records in accordance with quality standards Identify, report, and help investigate non-conformities or defects Support root cause analysis and corrective/preventive actions (CAPA) Ensure compliance with ISO, FDA, or other industry standards (as applicable) Communicate quality issues to relevant departments for resolution Participate in internal audits and continuous improvement initiatives Maintain a clean and organized inspection area in line with safety standards Requirements: High school diploma or GED; technical training or associate's degree is a plus 2+ years of experience in a quality inspection or manufacturing environment Proficient in the use of inspection tools and equipment Basic understanding of quality control procedures and statistical methods Ability to read technical drawings and specifications Strong attention to detail and documentation skills Familiarity with quality standards such as ISO 9001, AS9100, or similar Good verbal and written communication skills Ability to work independently and as part of a team Preferred Qualifications: Experience with GD&T (Geometric Dimensioning & Tolerancing) Knowledge of SPC (Statistical Process Control) Previous use of quality software (e.g., Minitab, QMS systems) Experience in manufacturing and aerospace Shift: 1st shift Pay: $19-22 an hour-based on experience About Cardinal Staffing Services:Cardinal Staffing Services, Inc. has over 25 years of experience being recognized as leaders in the staffing industry. Founded in Port Clinton, Ohio in 1994, we have grown and expanded into 5 states with 11 offices, delivering custom staffing and recruiting solutions to diverse markets. We leverage technologies, tools, and human connections to create the perfect environments to link employers and employees.We understand that finding the right job is about more than just a paycheck - it's about finding the opportunity that fits your skills, goals, and lifestyle. Here are the benefits you'll enjoy when you partner with us: Access to a wide range of job opportunities Competitive pay Health and Wellness Programs (including EAP) Medical benefits including medical, vision, dental, and prescriptions Electronic weekly pay Employee Advocacy & Personalized Job Support Cardinal Staffing also follows all applicable state and local laws regarding sick time, paid time off, and retirement savings programs. Cardinal Staffing is an equal opportunity employer.Our commitment to speed-to-hire means we work efficiently to get you placed in the right role, fast. If you're ready to take control of your career, explore exciting opportunities, and gain experience that lasts, then Cardinal Staffing is the place for you. Let's get started today! #IND1

At AAM, the POWER is in our people. We believe that an equitable and inclusive workplace benefits everyone, and that the diversity of our Associates drives creativity and innovation. Our global team is made of dreamers, doers and innovators who are Delivering POWER for a safer, brighter and more sustainable tomorrow. Job Posting Title Quality Tech Summary The successful Coordinate Measuring Machine (CMM) Programmer is one that is conscientious, detail orientated, and a self-starter able to work from a verbal or written instruction. They are committed to quality, precision, and timeliness in their deliverables. These deliverables are achieved while maintaining a safe and organized working environment. Job Description Final and in process inspection of tooling, components, and prototype parts using CMM and various gauges as required Ability to program and operate Zeiss CMM using Calypso software Ability to read blueprints and understand product specifications and requirements Ability to perform measurements of precision components to ensure specifications are met Ability to perform general shop math Ability to measure close tolerances Completion of customer inspection reports per instructions and requirements Performs preventive maintenance tasks as required Required Skills and Education High School Diploma About AAM: As a leading global Tier 1 Automotive and Mobility Supplier, AAM designs, engineers and manufactures Driveline and Metal Forming technologies to support electric, hybrid and internal combustion vehicles. Headquartered in Detroit with over 80 facilities in 18 countries, we are Bringing the Future Faster for a safer and more sustainable tomorrow. To learn more, visit AAM.com. Why Join #TeamAAM: As a member of #TeamAAM, you'll get to make a difference on day one. From your first day with us, you'll have the opportunity to grow, embrace challenges, build your skills, and bring your authentic self to work every day, all while helping to shape the future of mobility for AAM…and the world. AAM will not discriminate against any Associate or applicant for employment because of age, race, color, gender, religion, weight, height, marital status, sexual orientation, genetic history or information, gender identity or expression, disability, protected veteran status, national origin, or other characteristic protected by law. AAM will take affirmative action to ensure that applicants are employed, and that Associates are treated equally during employment, without regard to their age, race, color, gender, religion, weight, height, marital status, sexual orientation, genetic history or information, gender identity or expression, disability, protected veteran status, national origin, or other characteristic protected by law. For the Disabled Job Seeker: We offer reasonable accommodations for qualified disabled individuals who are applicants for employment. To request assistance or accommodations, please e-mail *************************. AAM is an equal opportunity/affirmative action employer.

Job Purpose Content for Job Profiles is a work in progress. If you need content to finalize this requisition for posting, please send a message to *************************. Job Duties and Responsibilities Job Description Content for Job Profiles is a work in progress. If you need content to finalize this requisition for posting, please send a message to *************************. Education and Qualifications Skills and Competencies Join our team of 40,000 problem solvers who are fostering a culture of innovation by leveraging the diverse perspectives of our global team. We believe in facing challenges head-on by finding opportunity and uncovering possibility, where roadblocks and barriers become targets instead of obstacles. We are One Dana with limitless opportunity. Our Values * Value Others * Inspire Innovation * Grow Responsibly * Win Together

Preferred Qualifications * Self-directed approach * Ability to communicate effectively * Proficiency in the Microsoft Office suite, including Excel, PowerPoint and Word Interns at the Rock Family of Companies gain priceless hands-on experience. Here, they learn how it feels to be in the workplace, participate in events and become a valuable member of our team. Responsibilities * Learn about our business by attending meetings, huddles and trainings * Share creative ideas that will help improve our business * Deliver reports, analyze metrics and summarize information to help drive our team forward * Assist in creating materials and/or presentations for meetings * Take notes during meetings and provide recaps Disclaimer This is an outline of the primary responsibilities of this position. As with everything in life, things change. The tasks and responsibilities can be changed, added to, removed, amended, deleted and modified at any time by the leadership group.

Job Title: Quality Technician - Injection Molding Company: Atomic Industries Reports To: Quality Manager Atomic Industries is reinventing how the world makes things. From cars and aerospace systems to medical devices and packaging, most physical goods begin life in a mold or are shaped by a manufacturing tool. Producing these tools has always been slow, manual, and dependent on scarce expertise, taking weeks or months. We're changing that. At our Detroit headquarters, we combine the industrial DNA of America's manufacturing heartland with the speed, intelligence, and precision of Silicon Valley. Our AI-driven platform tackles the hardest problems in geometry, process planning, and fabrication, collapsing production timelines from months to days and soon, minutes. We don't just build software; we run a fully operational factory where our technology produces production-grade tooling every week, enabling tight feedback loops and rapid iteration. Backed by top-tier investors, we're restoring speed, flexibility, and capability to the American industrial base. Our mission is to make manufacturing as agile and scalable as the digital world, and in doing so, rebuild the infrastructure of the physical economy. Position Overview We're seeking a detail-oriented and dependable Quality Technician to support quality control and inspection across our injection molding operations. You'll be on the floor inspecting parts, maintaining records, and working closely with process engineers and toolmakers to ensure every part meets Atomic's exacting standards. This is a key hands-on role as we scale high-volume production and build out our ISO-compliant quality systems. Key Responsibilities Perform visual and dimensional inspections of molded parts (first piece, in-process, and final) Use precision measuring tools (calipers, micrometers, height gauges, etc.) Assist with part qualification processes: FAI, PPAP, capability studies Record and maintain accurate inspection data and non-conformance reports Support containment, root cause analysis, and corrective actions Calibrate and maintain inspection tools per Atomic's calibration program Collaborate with operators, engineers, and quality manager on continuous improvement Follow and enforce safety and cleanliness standards on the shop floor Qualifications 2+ years of experience in a quality role in injection molding or precision manufacturing Proficient in reading technical drawings and GD&T Familiar with ISO 9001 quality systems and basic quality documentation Strong attention to detail and documentation discipline Comfortable using Microsoft Excel, Google Sheets, and quality tracking systems Bonus: experience with digital inspection equipment (CMM, vision systems) Work Environment Fast-paced, collaborative production floor Hands-on engagement with operators, engineers, and software teams Opportunity to grow into Quality Engineering or leadership roles as Atomic scales What You'll Get Competitive pay, benefits, and equity opportunity Exposure to next-gen manufacturing systems A seat at the table in building quality systems from the ground up

Department: Quality Assurance Job Title: Quality Assurance Associate Reports to: Quality Assurance Manager General Description The Quality Assurance Associate is a member of the Quality Assurance department responsible for overseeing and assisting in all aspects of Quality Systems Management. The QA associate role will function in two capacities: 1) Document generation, review, approval, and/or training in support of CGMP quality systems and operations, 2) QA on the floor during all manufacturing operations. DUTIES AND RESPONSIBILITIES Essential Duties and Responsibilities: 1. Develop, review, approve, and/or maintain documents that support both Quality Assurance and Operations. This may include Batch Records, Protocols and Reports (Engineering, Validation, Qualification, Stability, etc.), Risk Assessments, Process Flow Diagrams, Standard Operating Procedures (SOP's), Investigations, and any other technical documents as required, 2. Lead/represent QA on project teams in support of new product and manufacturing activities, 3. Review and approve incoming materials including but not limited to active pharmaceutical materials, excipients, components, and packaging materials, 4. Perform Quality oversight during manufacturing operations, including identifying and implementing process improvements through change control, investigations of non-conforming material, equipment, processes, etc., and review of the manufacturing documentation (batch records, logbooks, analytical testing data, protocol(s), etc.), 5. Perform review and approval of executed documents, 6. Assist in the identification, action, and resolution of changes and issues during manufacturing activities, 7. Develop and implement SOPs specifically related to CGMP quality systems, operations, and the facility, including training and training file maintenance, 8. Assist in management of quality systems on a company-wide basis, including document control, vendor quality, training, CAPA, change management, auditing, validation/qualification programs, and non-conformance investigations, 9. Other duties as defined by Biovire. Behavioral Expectations: 1. Strong work ethic and ability to accomplish tasks without supervision, 2. Demonstrate leadership both by words and leading by example to foster Biovire One Team culture, 3. Strong organizational skills and the ability to focus on multiple projects in a fast-paced work environment, 4. Excellent interpersonal skills with the ability to communicate effectively, 5. Basic computer skills (proficient in Microsoft Office applications), 6. Excellent communication skills, both written and verbal, 7. Possess honesty and integrity with a commitment to the highest legal and ethical standards, 8. Treats every person with courtesy and respect, 9. Knowledge of CGMP and regulatory principles, 10. Commitment to quality in the manufacturing process, 11. Ability to independently analyze and resolve complex issues, 12. Strong sense of initiative, accountability, and responsibility WORK EXPERIENCE AND EDUCATION REQUIREMENTS · BS in scientific discipline · 3+ years experience in the biotech/pharmaceutical industry preferred · Demonstrated knowledge and understanding of CGMP and CGMP Quality Systems

Department: Quality Assurance Job Title: Quality Assurance Associate Reports to: Quality Assurance Manager General Description The Quality Assurance Associate is a member of the Quality Assurance department responsible for overseeing and assisting in all aspects of Quality Systems Management. The QA associate role will function in two capacities: 1) Document generation, review, approval, and/or training in support of CGMP quality systems and operations, 2) QA on the floor during all manufacturing operations. DUTIES AND RESPONSIBILITIES Essential Duties and Responsibilities: 1. Develop, review, approve, and/or maintain documents that support both Quality Assurance and Operations. This may include Batch Records, Protocols and Reports (Engineering, Validation, Qualification, Stability, etc.), Risk Assessments, Process Flow Diagrams, Standard Operating Procedures (SOP's), Investigations, and any other technical documents as required, 2. Lead/represent QA on project teams in support of new product and manufacturing activities, 3. Review and approve incoming materials including but not limited to active pharmaceutical materials, excipients, components, and packaging materials, 4. Perform Quality oversight during manufacturing operations, including identifying and implementing process improvements through change control, investigations of non-conforming material, equipment, processes, etc., and review of the manufacturing documentation (batch records, logbooks, analytical testing data, protocol(s), etc.), 5. Perform review and approval of executed documents, 6. Assist in the identification, action, and resolution of changes and issues during manufacturing activities, 7. Develop and implement SOPs specifically related to CGMP quality systems, operations, and the facility, including training and training file maintenance, 8. Assist in management of quality systems on a company-wide basis, including document control, vendor quality, training, CAPA, change management, auditing, validation/qualification programs, and non-conformance investigations, 9. Other duties as defined by Biovire. Behavioral Expectations: 1. Strong work ethic and ability to accomplish tasks without supervision, 2. Demonstrate leadership both by words and leading by example to foster Biovire One Team culture, 3. Strong organizational skills and the ability to focus on multiple projects in a fast-paced work environment, 4. Excellent interpersonal skills with the ability to communicate effectively, 5. Basic computer skills (proficient in Microsoft Office applications), 6. Excellent communication skills, both written and verbal, 7. Possess honesty and integrity with a commitment to the highest legal and ethical standards, 8. Treats every person with courtesy and respect, 9. Knowledge of CGMP and regulatory principles, 10. Commitment to quality in the manufacturing process, 11. Ability to independently analyze and resolve complex issues, 12. Strong sense of initiative, accountability, and responsibility WORK EXPERIENCE AND EDUCATION REQUIREMENTS * BS in scientific discipline * 3+ years experience in the biotech/pharmaceutical industry preferred * Demonstrated knowledge and understanding of CGMP and CGMP Quality Systems

Responsible for Day-to-Day Quality activities and inspection operations, quality data requirements, and customer special measurement, reporting, or record requirements. Assist in the decision-making process regarding measurement or gaging of product characteristics, inspection planning, and/or reporting. Responsible for the calibration system and related documentation. Reports to the Quality Manager in matters of technical authority and responsibility. Rotate duties from each quality area to become proficient, and maintain proficiencies in all areas. Principle Responsibilities Uphold quality standards, concepts, practices and maintain customer satisfaction Assist in the development of processes to ensure quality requirements have been satisfied Identify, document and report non-conforming products or workmanship Maintain rework and scrap operating metrics Maintain staging and holding areas for inspection and non-conforming products respectively Calibration of inspection and measurement equipment using established guidelines Perform incoming receiving inspection on purchased special and standard components Perform PPAP analyses on incoming products Other tasks as deemed necessary by the Quality Manager Skills Required Basic computer and CAD knowledge Familiarity with the use of precision measuring equipment such as micrometers, calipers, height gage, optical comparator, hardness testers, surface finish tester, and CMM (open DMIS) Able to read blueprints and interpret G.D. & T. Understanding of ISO-9001:2015 standard Well organized Attentive to detail Strong communication skills. Proficient with Microsoft Office and ERP systems Education High school graduate or equivalent. Associates degree in Metrology and Calibration or similar technical field desired but not essential. Work Experience 2 - 5 years or more of related experience. Privacy Notice for California Residents P.C.S. Company (“PCS”) complies with the California Consumer Privacy Act (“CCPA”), California Privacy Rights Act (“CPRA”), and other applicable privacy laws. We may collect the following categories of personal information for purposes of the application and hiring process: name and contact information (phone number; mailing address; email address(es)); education and qualifications; employment history and experience; LinkedIn profile; and other information voluntarily provided by the applicant. Under the CCPA and CPRA, California residents have the right to know, correct, delete, and/or limit the use of certain information collected by PCS. For further information, see our full privacy policy at PCS Company - Privacy Notice for California Residents (pcs-company.com). If you have any concerns, please send an email to ******************.

Quality Technician Shift: 1st, 2nd, 3rd The Quality Technician uses specialized tools, skillsets, software and other implements to carry out quality activities at the direction of the quality supervisor. Technical activities like gaging parts, analyzing process capability/statistical process control data and controlling documents, gages and other vital records are just a few examples of what falls within the purview of the quality technician. ESSENTIAL FUNCTIONS: Collects, records, and disseminates data and information specific to quality functions such as Layered Process Audits, Document Control, Gage R&R and similar Responsible for updating production floor documents with performance data and distributing revised documents to the appropriate work centers/areas Coordinates with external vendors and suppliers for quality related activities such as calibration services, acquisition of certified standards, and other tasks as deemed necessary Assists in root cause analysis, corrective/preventative action implementation and identifying general continuous improvement opportunities within the scope of their responsibilities 5% Local travel; approximate 20-mile radius Additional duties with similar responsibilities may be assigned as necessary Requirements PHYSICAL DEMANDS/ENVIRONMENTAL CONDITIONS: The physical demands described below are representative of those that must be met by an employee to successfully perform the essential functions of this job. Able to stand/walk for the duration of shift (8+ hours) Able to lift up to 40lbs unassisted Able to perform frequent repetitive motions Able to withstand noisy environment Work station is in a shared and open environment TRAVEL REQUIREMENTS: 5% Local travel; approximate 20-mile radius EMPLOYMENT REQUIREMENTS: High school diploma or GED 3-5 years experience higher level of self-motivation and practical competence in the areas and activities for which they are responsible An intermediate understanding of quality standards, documentation and practices is also required Depending on the duties assigned, familiarity with specialized software such as Access, Minitab, Gage Track, QAD and others may also be necessary Reliable transportation Proficient in Microsoft Office Suite Able to read, write and speak English

Job Description Coplas Inc. an affiliate of Tiercon Corp. is an automotive supplier committed to the design, manufacture and assembly of quality exterior trim and assembled systems used as original equipment in the automotive market. Headquartered in Sterling Heights Michigan, Coplas employs approximately 50 employees. Coplas is seeking knowledgeable, self-directed, experienced and hardworking individuals interested in the automotive industry as a Quality Technician. Job Summary & Reporting Structure: Reporting to the Assistant Quality Manager or designate, the Quality Team Leader is responsible for ensuring quality requirements on the production floor are met. They will be responsible for maintaining workflows in production by monitoring steps of the process; training production employees, correcting quality concerns and at all times ensuring the ongoing adherence to the policies and procedures outlined in the ISO9001:2015 AND IATF 16949 Quality System and encouraging continuous improvement wherever possible. Responsibilities: Responsible for the quality of products in accordance with Company Quality Policy and Objectives Perform duties that reflect compliance to Company's Quality Management System (QMS) as recorded in the organization's Quality Manual Participate in PPAP, PFMEA, Control Plans and Gauge R&R Demonstrate conformance to regulations recorded in supplied Employee Handbook Perform quality inspection duties (first/last off, in process inspections) Train new and existing employees Maintain all controlled document files and test records in a timely and accurate manner Visually inspect produced parts for defects and reports flaws immediately to management Measure and check fixtures, record data in spreadsheets. Perform data analysis to ensure accuracy of production requirements. Disposition nonconforming parts into appropriate container to prevent contamination of finished goods Detect and report machine malfunctions promptly to management and immediately notify Supervisor or Quality of all discrepancies to established quality checks (ie, sample boards, inspection instructions, Quality Alerts, etc.) Package and transports produced parts as needed Participate in team problem solving activities (ie, 8D's, communication meetings, etc.) Responsible for following all internal and OSHA required safety procedures Resolve problems by analyzing data, investigate issues, identify solutions, recommend corrective action in accordance with continuous improvement initiatives Track and submits statistics on the cost of poor quality Track performance of layered audits (e.g. track number of audits completed) Troubleshoot equipment problems to ensure quality and efficiency Able to stand for long periods and lift up to 45 pounds Promote continuous improvement in all areas Other duties as assigned ISO9001:2015 AND IATF 16949 duties as required Qualifications: Demonstrated working knowledge in PPAP, PFMEA, Control Plan & Gauge R&R High School Diploma or Equivalent work experience at minimum 2 years prior work experience in plastics or automotive industry is an asset Manufacturing experience Supervision experience an asset Training Effective communication skills, verbal, and written Computer skills data analysis Ability to using various measurement techniques Strong prioritization skills Manual dexterity skills Good attention to detail Coplas Inc. is proud to be an inclusive and equal opportunity employer. At Coplas we are committed to ensuring the workplace is free from discrimination. Coplas welcomes and encourages applications from everyone including persons with disabilities. During our hiring process, we will notify job applicants that accommodations are available upon request. If a selected job applicant requests accommodation, Coplas will consult with the individual and provide or arrange for the appropriate accommodation taking into account the applicant's disability-related needs. Please contact Tiercon Human Resources at **************. The Prevue ATS uses AI technology to match candidates to job opportunities. Please see the Terms of Service for full details

Quality techs are needed at a brand new Automotive facility in Lake Orion. . You have to be able to use measuring devices like micrometers and calipers, gage the parts, report them and make sure production is running smoothly. At least 1 year of experience. Split shift and afternoon shift available. 1:30pm-10pm Monday-Friday at $18/hr Respond to this add or call ************.

Job DescriptionDescription: The Quality Technician supports the company's quality assurance and continuous improvement processes by performing inspections, maintaining documentation, and ensuring compliance with customer and company standards. This role is responsible for executing quality control activities, managing nonconformance documentation, and providing accurate data to support production and customer satisfaction. Requirements: Responsibilities: Input and maintain records for Nonconformances (NCs), Return Material Authorizations (RMAs), and Vendor Returns (VRs) in the quality system. Support communication with customers regarding quality issues, corrective actions, and compliance status. Review and validate orders for compliance with customer terms, specifications, and quality requirements. Operate and program Coordinate Measuring Machines (CMMs) to inspect components and verify conformance to specifications. Perform and record gage calibration and verification activities to ensure measurement accuracy and compliance. Participate in internal audits to verify adherence to ISO and company quality standards; document findings and support corrective actions. Create and maintain balloon drawings, inspection plans, and test documentation for production and quality processes. Assist in identifying opportunities to improve processes, reduce defects, and strengthen quality systems. Support Quality Inspectors by assisting with daily inspection activities and cross-train to perform inspection duties as needed. Other duties as assigned Qualifications: Associate degree or technical certification in Quality, Manufacturing, Engineering, or a related field preferred. 2+ years of experience in a manufacturing quality or inspection role. Working knowledge of CMM operation and metrology principles. Familiarity with ISO 9001 or other quality management systems. Proficient in Microsoft Office and quality software systems (ERP, QMS). Strong attention to detail, organization, and communication skills.

About Rhino Tool House: Our mission is to identify and deliver the world's most innovative industrial solutions. We provide superior service, local expertise, and a high degree of responsiveness to empower our customers to be more productive, build a better-quality product, and maintain a safe environment for their workers. Job Description: The Quality Technician is responsible for performing inspections, tests, and audits to ensure products and processes meet established quality standards. This role works closely with production, engineering, and operations teams to identify nonconformities, assist in root cause analysis, and support continuous improvement initiatives. Key Responsibilities: · Perform incoming, in-process, and final inspections on parts, assemblies, and finished products. · Verify products meet specifications by using precision measuring instruments (calipers, micrometers, gauges, etc.). · Document inspection results, maintain quality records, and prepare reports. · Assist in root cause analysis and corrective/preventive action activities. · Support calibration and maintenance of inspection tools and equipment. · Ensure compliance with company procedures, ISO standards, and customer requirements. · Collaborate with production teams to resolve quality issues in a timely manner. · Participate in continuous improvement, 5S, and lean manufacturing initiatives. · Escalate quality concerns and recommend improvements to reduce defects and scrap. Qualifications: · High school diploma or equivalent required; technical certification or associate degree preferred. · 1-3 years of experience in quality inspection or quality assurance within manufacturing or industrial environments. · Knowledge of ISO standards, quality systems, and inspection processes. · Proficient in using measurement tools (calipers, micrometers, height gauges, etc.). · Basic understanding of engineering drawings, GD&T, and specifications. · Strong attention to detail, accuracy, and problem-solving skills. · Proficiency with Microsoft Office; experience with ERP/QMS software a plus. · Strong communication and teamwork abilities. Physical Requirements: · Ability to stand, walk, bend, sit, and lift up to 50 lbs. as needed. · Comfortable operating forklifts, pallet jacks, and other warehouse equipment. · Work in a manufacturing / warehouse environment with varying temperatures and noise levels.

Our mission is to identify and deliver the world's most innovative industrial solutions. We provide superior service, local expertise, and a high degree of responsiveness to empower our customers to be more productive, build a better-quality product, and maintain a safe environment for their workers. Job Description: The Quality Technician is responsible for performing inspections, tests, and audits to ensure products and processes meet established quality standards. This role works closely with production, engineering, and operations teams to identify nonconformities, assist in root cause analysis, and support continuous improvement initiatives. Key Responsibilities: · Perform incoming, in-process, and final inspections on parts, assemblies, and finished products. · Verify products meet specifications by using precision measuring instruments (calipers, micrometers, gauges, etc.). · Document inspection results, maintain quality records, and prepare reports. · Assist in root cause analysis and corrective/preventive action activities. · Support calibration and maintenance of inspection tools and equipment. · Ensure compliance with company procedures, ISO standards, and customer requirements. · Collaborate with production teams to resolve quality issues in a timely manner. · Participate in continuous improvement, 5S, and lean manufacturing initiatives. · Escalate quality concerns and recommend improvements to reduce defects and scrap. Qualifications: · High school diploma or equivalent required; technical certification or associate degree preferred. · 1-3 years of experience in quality inspection or quality assurance within manufacturing or industrial environments. · Knowledge of ISO standards, quality systems, and inspection processes. · Proficient in using measurement tools (calipers, micrometers, height gauges, etc.). · Basic understanding of engineering drawings, GD&T, and specifications. · Strong attention to detail, accuracy, and problem-solving skills. · Proficiency with Microsoft Office; experience with ERP/QMS software a plus. · Strong communication and teamwork abilities. Physical Requirements: · Ability to stand, walk, bend, sit, and lift up to 50 lbs. as needed. · Comfortable operating forklifts, pallet jacks, and other warehouse equipment. · Work in a manufacturing / warehouse environment with varying temperatures and noise levels.

Our company specializes in manufacturing re-usable plastic packaging and is a leader in the thermoforming industry. We are currently looking for motivated individuals to join our team as a Quality Technician. Quality Technicians are in responsible for supporting the Quality Manager and production team to ensure parts are made to customer specifications. Technicians will utilize the MES to record their testing. Reports to: Quality Manager Shift: 3:30 PM - 2:00 AM Monday - Thursday Responsibilities: Assist Quality Assurance and Production staff by providing expertise to resolve quality issues Inspect and validate incoming parts from external companies Use hand tools such as tape measure and micrometers to inspect and test internally produced components/parts to ensure quality and system requirements are met Understand quality tolerance and GD&T Qualifications: Previous experience a quality position Strong Computer Skills Strong Organization Skills Familiarity with plant tools and equipment Strong troubleshooting and critical thinking skills Ability to Lift up to 50 pounds Ability to stand for 8+ hours Ability to thrive in a fast-paced environment Benefits: Starting pay: $19.00/hr plus .75 shift premium Health, Dental, Vision, Life Insurance after 60 days 401k with 50% employer match up to 6% after 90 days Paid Time Off, Holiday Pay, Paid Sick Leave Career advancement opportunities

As a Quality Technician, you have the understanding of and will perform intermediate SAP transactions, possess the technical knowledge to complete quality checks on multiple lines or areas in a department or site, depending on the size of facility, you may actively trains associates in the Quality Technician role and/or others, demonstrates the interpersonal skills needed to transfer job knowledge to trainees, will be a contributing member of the Internal Audit team. You Will · Be capable of Testing Product: o May create new product in SAP test plan o Conduct qualifications o Comprehends PPK, trends, runs, etc. o Create 1st article in SAP o Completes all measurement requirements per package o Identifies out of spec and out of control data o Uses all required testing equipment properly · Understand basic SAP/Iconics Transactions: o May modify test plans, including specs and test frequency o Comprehends PPK, trends, runs, etc. o Scrap heldware through SAP o Enter SPC data in SAP o Enter Near Miss/1 on 1 and Find It Fix It o Create shift reports o Basic understanding of Excel and other Office tools · Monitor Product Parameters o Review critical product charts beyond daily testing o Identify invalid data o Review product charts during daily testing · Handle Non-Conforming Product: o Place product on hold in multiple bins, including outside warehouse and bins that aren't the 210 hold o Correct heldware inventory discrepancies with the help of warehouse o Audit till defect free o Use Target, Acceptable, Marginal, Unacceptable inspections (TAMU)'s to identify visual defects · Resolve equipment issues and make minor adjustments: o Troubleshoot most issues on testing equipment, including the hot filler o Work with maintenance as needed to get equipment running o Identify when quality equipment isn't working correctly o Basic troubleshooting ability to get quality equipment operational · Participate in other aspects of the Quality Management System: o Conducts mock recalls with limited help o Conducts calibration on most equipment and works directly with vendor for external service o Understands the basics of a mock recall o Understands the basics of calibration · Miscellaneous duties as assigned o Capable of training quality You Have · Ability to work 12-hour rotational shift 7:48ampm - 8:00am (2B) · High School Diploma, GED, or equivalent · Minimum of one to three year(s) of related experience · Working knowledge of quality control methods & approaches · Superior attention to detail · Ability to walk & stand on production floor throughout work shift with or without a reasonable accommodation As a Plastipak Associate, you receive a benefits package offering the following: Wellness Programs Health Insurance Coverage, including Medical, Dental & Vision EAP, Employee Assistance Program Life Insurance Accidental Death & Dismemberment Insurance Disability Insurance: Short-Term & Long-Term Accidental Insurance Critical Illness Insurance Hospital Indemnity Insurance 401(k) Plan, with Company Matching Contribution & Profit Sharing feature Paid Time Off - 80 hours within 1st year & subsequent increases Paid Company Holidays Dependent Care Flexible Spending Account Caregiving via Care.com Pet Insurance Tuition Assistance Program Sons and Daughters Scholarship Program Travel Assistance Employee Discount Programs *Some benefits are subject to eligibility requirements Plastipak is an Equal Opportunity Employer In order to process your job application, Plastipak collects and stores the personal information that you submit via this website. Please refer to Plastipak's to understand how Plastipak uses and protects the information that you provide.

Job DescriptionSalary: DOE Witco is looking for a talented and experienced addition to our quality team! The ideal candidate will have experience in a Quality Control environment working with machined components in all phases of inspection, and will have CMM experience. This position will be working on the floor and in the quality lab under the direction of the Quality Manager. If you like a day that flies by, the challenge of finding new ways to check parts, assisting with problem solving tasks, and are not afraid of paperwork, then this is your next adventure! Responsibilities: Calibrate measuring equipment First piece and in process inspections Receiving inspections Final inspections Supplier Certification Review Floor audits Document non-conforming material Create gage sheets Tag non-conforming material Create inspection reports Required experience: MUST be able to perform calibrations using all standard gaging to check tight tolerances. CMM programming and operation experience, ideally using Zeiss Calypso software or equivalent. A comprehensive understanding of AS9100 and/or ISO9001:2015 Quality Management Systems. Details: Full Time Employment with excellent benefits package including medical, dental, vision, and life insurance, 401K plan, pre-tax AFLAC offerings, and more. Monday Friday 6:00am 4:30pm Lunch 12:00pm 12:30pm Located near Yale, Michigan, Witco Inc. is a precision CNC Turning, Milling, and Gear Cutting company that services various global industries, including Aerospace, Medical, Defense, Metal Mining, Oil and Gas, and Outdoor Sporting Goods. We are a short run facility with typical build sizes ranging from 10-pieces to 1000-pieces. To Apply: Forward a resume by replying to this job posting. Witco Inc. is an equal opportunity employer and will not discriminate against any applicant on the basis of any characteristic that is protected by State or Federal law.

QUALITY TECHNICIAN 2nd SHIFT 2:30 PM - 11:00 PM MISSION To create new value, excite and delight our customers through the best automotive products and services. We value integrity, customer focus, creativity, with efficient and nimble actions and respect highly motivated people with team spirit. JOB SUMMARY: Support manufacturing by guiding, training, and covering floor receiving, shipping, and manufacturing activities to reduce customer exposure and excessive internal waste. ESSENTIAL FUNCTIONS: Supports manufacturing validation, and verification of product quality standards. Reviews daily shutdown / stop notices and reports trends / further actions as appropriate. Participates and leads floor audit activities and action plans. Verify equipment used for part validation is appropriate for use. CONTROL OF NON-CONFORMING PRODUCT: Monitors sort/rework activities and confirms product is identified during all stages and records are maintained. Trains sort staff and audits sort activities to validate effectiveness FINAL AUDIT: Performs sampling audit on all shipments, and maintains shipment audit records Verifies that containers are identified correctly Assures that suspect material is identified and placed in the designated quarantine area to prevent shipment EDUCATION AND EXPERIENCE: Minimum of 2 years of manufacturing quality experience. Quality systems experience or training required. Basic computer skills and required. Previous experience using Plex software preferred. Job Type: Full-time Benefits: 401(k) matching Dental insurance Health insurance Health savings account Life insurance Paid time off Referral program Vision insurance Schedule: 8 hour shift Day shift Monday to Friday Weekends as needed Experience: Quality: 2 years (Required) Stamping: 3 years (Required) Plex: 2 years (Preferred) Shift availability: 2 nd Shift (Required)