Quality control technician jobs in Flint, MI

***$3,000 sign-on bonus*** ™ MediVera Compounding Pharmacy™ is a second-generation family-owned business that cares deeply about its employees. We are dedicated to providing personalized medication solutions to meet the unique needs of our patients. Our culture emphasizes hard work, positive team spirit, and embracing a growth mindset. We have a family-friendly work environment and are proud to offer an unrivaled culture based around our identified core values below. We collaborate closely with healthcare providers to ensure the highest quality and efficacy of our compounded medications. We offer full benefits, generous PTO, tremendous bonus opportunities, and aggressive growth potential. Job Overview The Sterile Lab Technician plays a critical role in producing safe, high-quality sterile compounded medications that directly impact patient health and outcomes. Operating within MediVera's USP / cleanroom suite, this role performs aseptic compounding, maintains regulatory compliance, and safeguards the integrity of our sterile production environment. This position is ideal for someone who takes pride in precision work, thrives in a controlled and fast-paced setting, and brings a proactive, growth-oriented mindset to every task. As part of a highly collaborative team-including pharmacists, supervisors, and fellow technicians-you will contribute to continuous improvement, uphold MediVera's core values, and support our mission of helping one patient at a time live their best life. Job Responsibilities: Performs sterile compounding using validated aseptic techniques in compliance with USP , , and state/federal regulations, ensuring every product meets MediVera's high quality standards. Maintains the ISO-classified cleanroom environment through daily/weekly cleaning, sanitization, and environmental control tasks, demonstrating respect for all by ensuring patient-safe conditions. Executes production activities including equipment setup, labeling, calculations, filtration, and documentation with accuracy, detail, and pride in everything you do. Supports production planning by preparing batches, staging materials, and collaborating with pharmacists and supervisors to meet daily compounding goals. Participates in continuous improvement initiatives-such as 5S, root cause analysis, and waste reduction-to enhance workflow efficiency and embody a growth mindset. Conducts quality support activities such as visual inspection, sample handling, cleaning validations, and inventory rotation (FIFO), demonstrating positive team spirit. Ensures proper garbing, gowning, and adherence to cleanroom behavioral expectations at all times to protect product sterility and team safety. Communicates effectively with supervisors, pharmacists, and peers regarding workload, equipment issues, and process improvements, contributing to a collaborative and respectful work environment. Attributes & Skills Prior experience as sterile compounding pharmacy technician. Certified Pharmacy Technician (CPhT) or ability to obtain within required timeframe. Strong understanding of sterile technique, aseptic behavior, and cleanroom operations. Ability to follow detailed written procedures, compounding formulas, and batch records. Skilled in basic math calculations, measurements, and accuracy-driven tasks. Comfortable working in PPE, including masks, gowns, gloves, and sterile garb for extended periods. Excellent organizational and time-management skills with the ability to prioritize tasks in a high-paced production environment. Strong sense of ownership and accountability for work output and cleanroom compliance. This job description reflects our commitment to have respect for all, take pride in everything you do, embrace a growth mindset, work your hardest, and display positive team spirit in all aspects of our organization. MediVera is different. Here, you're not just another employee-you're part of a team that's rewriting what pharmacy work can feel like. We're family-owned, fiercely independent, and unapologetically built around people, not profits. At MediVera: You matter. Your work directly improves lives, not just corporate earnings. You're seen. Our leadership isn't hidden in glass towers-they walk the floor, know your name, and value your input. You belong. Our culture is non-negotiable: respect, passion, pride, growth, and teamwork aren't slogans, they're how we live. You make impact. Every idea, every contribution helps shape how we grow and how we serve patients. Here, you're not just filling prescriptions. You're filling a purpose. You're shaping lives. You're fueling a mission that matters. You're helping one patient at a time live their best life! If you're tired of being a number, tired of stress without meaning, and ready to be part of something real-this is where you belong.

Setting: Hospital? Are you ready to take your expertise as a cardiovascular technologist to new heights? Join Jackson HealthPros as a cath lab tech (Cardiovascular Invasive Specialist) and play a vital role on a team that values your expertise-while enjoying the excitement of a new location. Earn full time pay and benefits while you assist physicians and other Cath lab personnel in conducting vital diagnostic tests and procedures; and operate advanced medical equipment to capture crucial images and data of the heart and blood vessels. What You'll Need: ARRT certified Radiologic Technologist Registered Cardiovascular Invasive Specialist (RCIS) certification from Cardiovascular Credentialing International (CCI) preferred. Must have 2 years' experience in a Cath Lab hospital setting BLS & ACLS Certification (American Heart Association preferred) State specific licensing when required Apply now and you'll be contacted by a recruiter who'll fill you in with the details. Benefits Designed for Travelers We deeply value your commitment to impacting others, that's why we offer a comprehensive and competitive benefits package starting your first day. Weekly, On-Time Pay because that's how it should be Full Medical Benefits & 401k Matching Plan 24/7 Recruiter: Your main point of contact available by text, phone or email Competitive Referral Bonuses 100% Paid Housing Available Travel & License Reimbursement Impacting the Quality of Care for Patients Nationwide As a healthcare professional with Jackson HealthPros, you get the flexibility, stability and growth you need with the satisfaction of impacting communities nationwide. Choose from a variety of career options including direct hire, temp-to-hire, and travel contracts in cities coast to coast. Get full-time pay, benefits, and relocation assistance (at no cost to you) in travel contracts that give you the freedom to explore, with the stability of a full-time job. Find your perfect match with ProVenture, our AI enhanced career app designed just for you. EEO Statement Jackson Healthcare and its family of companies are an EEO/AA Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sexual orientation, gender, gender identity and expression, national origin, age, disability or protected veteran status. We celebrate diversity and are committed to creating an inclusive environment for all of our associates. Join our team as a traveling Physical Therapist where you'll help patients recover from injuries and manage chronic conditions while experiencing life in a new location. Apply now and we'll connect you with a recruiter who'll reach out with more details.

Kelly is hiring an Associate Laboratory Technician for a 6 -month Contract role with one of our prestigious clients based out in Troy, MI 48083. Job Title: Associate Laboratory Technician Employment Type: 6-month contract Pay rate: $21-23.50/hr. Shift: 7 am - 4 pm Qualifications: • Excellent safety record and fundamental knowledge of pilot plant and or laboratory safety • Experience in lab operations, including use of computer control • Mechanical aptitude for operating and troubleshooting lab equipment • Ability to run or learn to run analytical tests required to support pilot plant operations • Excellent teamwork with the ability to manage all aspects of executing test plans supporting required by run engineers/technical liaisons. • Commitment to data quality • Attention to details • Flexibility to adapt to changing priorities Responsibilities: • Safely operate and maintain Lab equipment • Provide support for third party vendors performing required equipment calibration • Conduct lab test according to lab testing procedures • Record test results on computerized SPC charts • Communicate with operators and business group representatives • Maintain lab supplies • Attend unit pre-trial meetings • Participate in equipment safety reviews • Work independently as the only testing technician in the lab Conduct polymer property testing using the following equipment: Hardness Gauges APA LCR Tensile Tester Moisture analyzer Mahr tester Run small extruder Color use Hunter Lab scan Die Cutter Density Tester Injection molding If you believe you are a good fit for this opportunity, please submit your application through the job posting link. We also encourage you to share references if you have them.

At DuPont, our purpose is to empower the world with essential innovations to thrive. We work on things that matter. Whether it's providing clean water to more than a billion people on the planet, producing materials that are essential in everyday technology devices from smartphones to electric vehicles, or protecting workers around the world. Discover the many reasons the world's most talented people are choosing to work at DuPont. Why Join Us | DuPont Careers DuPont has an immediate opening for a Quality Control Laboratory Tester at our Healthcare Industries Materials Site located in Hemlock, MI. The DuPont Healthcare Industries Materials Site produces products for use in the Biopharmaceutical, Pharmaceutical, Medical, and Cosmetic Industries. The site has been in continuous operation since 1964, dedicated to Healthcare products. Our products are distributed globally and are recognized as World Class for quality. The Laboratory is staffed 12 hours per day, 365 days per year, excluding some holidays or other site shutdown events. The lab is staffed in a 2-3-2 non-rotating 12-hour shift schedule. The Lab Testers are on-call for in-process testing during the off-shift. RESPONSIBILITIES DESCRIPTION Your key responsibilities will be/what you'll do: Testing raw materials and finished products to ensure quality standards and specifications are met Inspection of incoming raw materials and chemical intermediates to assure quality before use in production Troubleshooting process problems and evaluating process improvements Testing includes use of complex and sensitive instrumentation and techniques including but not limited to: Gas Chromatography, Fourier Transform Infrared Spectroscopy, Physical properties of polymer by Instron Tensometer, Centrifuge, pH. Assay by solvent extraction, Titration, Penetrometer, Mixers, Balances, Pipettes, Computers, Ovens, Incubators, Microscope, Air samplers, Particle Counters, and X-Ray Fluorescence Spectroscopy JOB QUALIFICATIONS Requirements: A High School Diploma or GED is required; a Bachelor's degree in the Sciences, Engineering, or Computer Science is preferred 2+ years of lab experience with some experience in an industrial setting is required; Experience with SAP is preferred Familiarity with Good Manufacturing Practices such as 21 CFR 210/211/820, ICH Qx, United States Pharmacopeia (USP), European Pharmacopeia (PhEur), Chinese Pharmacopeia (ChP), Japanese Pharmacopeia, ISO 9001 2015, and ISO 14001 is preferred Please note that a minimum requirement for this U.S. based position is the ability to work legally in the United States; no visa sponsorship/support or relocation assistance is available for this position. Join our Talent Community to stay connected with us! DuPont is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information. DuPont offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page.

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 DescriptionDescription: Perform quality testing on products manufactured by organization and incoming products as required to ensure quality standards for the products are met. Primary Functions and Responsibilities Self-organized control of raw materials and finished polyurethane resins Conduct analysis of the samples Compile data and interpret the results using standard procedures to determine compliance with specifications. Document and record data evaluate correctness of results Product certificates of conformance Organization and storage of test samples Block raw materials if properties don't meet specifications Block finished goods if properties don't meet specifications and/or quality standards Perform periodic preventive maintenance and calibration of lab equipment Ensure that supplies and equipment are maintained at an adequate level. Works following all safety policies and procedures in the lab Report inconsistencies, malfunctions and/or variations Performs other duties as assigned Requirements: Knowledge, Skills and Abilities Ability to plan, organize and take initiative Good oral and written communication skills Knowledge of basic statistics Neat and organized Chemical knowledge helpful Minimum Qualifications Microsoft office suite Attention to detail Experience working in a lab setting preferred Work Environment Lab setting Hours will be 8am-5pm

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

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 ************.

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 ******************.

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.

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

Job Description 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

Temp About the job Team: Quality Control/Purchasing Reports to: Purchasing Type: Full-time (Mon-Fri) Be the front line for our customers and suppliers. The right person is organized, metals-literate, and results-oriented. What you'll do Keep the ISO 9001:2015 program audit-ready: documents, internal audits, corrective actions, and the annual surveillance audit schedule. Own training records and the skills matrix; track recertification's. Run day-to-day quality checks (incoming, in-process, final), hold/release, and basic calibration scheduling. Handle supplier & customer claims: NCR/RMA, root cause, corrective action, and cost recovery. Buy and coordinate metal (coil/flat-rolled) from approved suppliers: issue POs, confirm lead times, track deliveries, and expedite when needed. Keep ERP/MRP data clean (lot/heat traceability, certs/COAs) and share clear updates with operations & sales. What you'll bring 2-6+ years in a metals service center, stamper, coil processor, or similar quality and/or purchasing role. Working knowledge of ISO 9001:2015 and internal audits (formal auditor cert is a plus). Comfortable reading mill certs, alloys/tempers, gauges, and customer specs. Solid Excel/Sheets; experience with ERP/MRP (Epicor/Infor/NetSuite/JobBOSS or similar). Problem-solving chops (5-Why/8D/SPC basics) and clear communication with mills, customers, and the shop. Success metrics (first 6-12 months) Quote cycle time and win rate at/above target OTIF on your book = target; proactive communication on exceptions Accurate orders (right alloy/temper/gauge/packaging) and low rework Clean data hygiene: acknowledgments, confirmations, next steps always current Positive customer feedback; internal teams find you reliable and prepared Compensation (Michigan market guidance) Cross-trained role-quality + buying-great visibility and career growth (Senior Coordinator/Lead). Competitive hourly pay $26-$35/hr depending on experience. Benefits include: 401K with 3% company match; PTO; medical, dental and vision with company paying 70% of you and your families premium; bonus program; tuition reimbursement.

Quality Technician (Production) III / IV Who we are… We are a team of scientists, engineers, technicians, and innovators dedicated to changing the world by developing medical isotopes to treat and eradicate cancer. We believe in building an environment where collaboration, curiosity, and camaraderie thrive. We also enjoy darts, cornhole, ping-pong, chili cook-offs, and other fun events that make our company a community where we make a life, not just a living. Who you are… You love details and precision. You find standardized work in which deviation could cause an undesirable outcome to be invigorating. Analyzing processes and results to control variations and discussing when improvements would best be introduced is a desirable pastime. Words that describe you are dedicated, efficient, and someone who contributes to making the workday fly by with engaging conversation and team comradery. How you make an impact… You'll provide instrumental support within the quality team and throughout the company to ensure timely product and compliance support. Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to our partners and patients. Our science and risk-based compliant quality culture is innovative and partner oriented. Whether you are involved in manufacturing, testing, or compliance, your contribution will directly impact patients. What you will achieve… Drive quality and compliance, adhering to all Quality Systems documentation requirements and establishing/supporting plans to exceed Niowave's goals for Quality, including Safety, Compliance, Six Sigma Quality, On-Time Delivery (OTD), and financial objectives. Support internal and external audits; support validation of test methods, monitoring processes, and equipment. Support new product introduction (NPI) quality activities including prototype testing, process validation, and technology transfer ensure successful product launches. Lead and participate in product/material hold, release, disposition, and traceability assessments, and implement improvements to reduce recurring deviations that lead to rework or scrap. Lead or support teams through out of tolerance, nonconformances, complaints, and CAPA investigations. Lead or support teams through change control that support continuous improvement and other needs. Lead or support Quality Assurance (QA) with completing quality checks and approvals on production records. What you need to succeed… Associates or Bachelor degree or equivalent in science or other related field. 5+ years related experience, with a solid understanding of regulatory compliance related to operations and quality procedures. Experience in quality assurance or quality control roles within a manufacturing or industrial environment. Knowledge and experience in eQMS, Inspection, Measuring and Test Equipment (IMTE) management systems, statistical process control (SPC), and root cause analysis methodologies (Six Sigma RCA). Embraces and models the Niowave Values of Teamwork, Courage, Integrity, and Upright Zeal. Understands how to integrate into a new team/organization - appreciates the history of current state, know how and when to make suggestions, as well as using just the right pace to reach the improved future state. Understands their own communication and learning styles, can assess others' styles, and is able to find the right path to connect the two. Great to have… Certification in quality management or related field (e.g., Certified Quality Technician/Engineer, Six Sigma). Experience in a facility with radiation regulatory requirements and or quality assurance experience with pharmaceuticals or medical devices. Experience with Minitab, JMP or other analytical tools. Experience in audits (internal, NRC, FDA, etc.). Knowledge of ISO 13485, 21 CFR 820, 21 CFR 210/211, and Nuclear Regulatory Commission (NRC) regulations or similar regulatory compliance experience. Work Environment The company's standard operating hours are Monday thru Friday 6a - 6p with production related activities requiring 24/7/365 shifts. This position will have regular working hours during M - F with an expectation of adjusting to operational commitments as needed. Niowave has multiple locations within the Lansing area. Travel between locations is expected in the role. While performing the duties of this job, the employee is occasionally required to: use hands to finger, handle, or feel objects, tools, or controls; reach with hands and arms; climb stairs; walk throughout all locations of the company; talk and hear; wear safety glasses, googles, gloves, lab coat and/or Tyvek suit. The employee must occasionally lift or move office products and supplies, up to 25 pounds. This position may stand and sit for prolonged periods. Please provide a cover letter specifically describing the nature of your interest & expertise.

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.

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

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