Travel Cath Lab Tech
Quality assurance technician job in Grand Blanc, MI
Company: Fusion Medical Staffing
Job Details
Fusion Medical Staffing is seeking a skilled Cath Lab Tech for a 13-week travel assignment in Grand Blanc, Michigan. As a member of our team, you'll have the opportunity to make a positive impact on the lives of patients while enjoying competitive pay, comprehensive benefits, and the support of a dedicated clinical team.
Required Qualifications:
One year's recent experience as a Cardiac Cath Lab Tech
Current BLS (AHA/ARC) certification
ARRT, RCES, or RCIS certification
Current ACLS (AHA/ARC) certification
Preferred Qualifications:
Valid Radiologic Technologist license in compliance within state regulations
PALS (AHA/ARC) or ENPC Certifications
Other certifications and licenses may be required for this position
Summary:
The Cath Lab Technologist is responsible for assisting in diagnostic and interventional cardiovascular procedures in the cardiac catheterization lab. This role involves preparing patients and equipment, monitoring hemodynamic data, assisting physicians during procedures, and ensuring patient safety throughout the process. The technologist operates specialized imaging equipment, maintains sterile technique, and collaborates with the healthcare team to provide high-quality patient care. This position requires technical expertise in cardiovascular procedures, critical thinking skills, and the ability to work efficiently in high-pressure situations.
Essential Work Functions:
Prepare and position patients for cardiac catheterization, angioplasty, stent placement, electrophysiology studies, and other interventional procedures
Assist physicians during procedures by passing catheters, wires, balloons, and stents, and operating fluoroscopy and hemodynamic monitoring equipment
Operate and maintain imaging equipment, contrast injectors, and hemodynamic monitoring systems, ensuring proper functionality
Scrub in and assist with sterile field setup, ensuring adherence to infection control and procedural protocols
Perform sheath removal and hemostasis using manual compression or closure devices as directed
Maintain accurate documentation, including patient records, imaging data, and equipment logs
Assist with inventory management, stocking supplies, and ensuring proper storage of sterile instruments and medications
Adhere to radiation safety protocols, ensuring proper use of lead aprons, shields, and dosimeters
Ensure compliance with hospital policies, safety guidelines, and regulatory requirements
Adhere to hospital safety protocols, infection control guidelines, and regulatory standards
Perform other duties as assigned within the scope of practice
Required Essential Skills:
Critical thinking, service excellence, and good interpersonal communication skills
The ability to read, write, and communicate in the English language
Ability to read/comprehend written instructions, follow verbal instructions, and proficiency in PC skills
Physical Abilities - Must be able to remain in a stationary position, move about, move equipment (50-100lbs), push, pull, and bend
Interpersonal Skills - Must be able to work effectively with a variety of personnel (professional and ancillary) to present a positive attitude and professionalism
Technical/Motor Skills - Must have the ability to grasp, perform fine manipulation, push/pull, and move about when assisting with procedures and/or using department equipment
Mental Requirements - Must be able to cope with frequent contact with the general public and customers while meeting deadlines under pressure. Must be able to work under close supervision occasionally, as well as working without assistance from other personnel. Must be able to contend with irregular activity schedules occasionally and continuous concentration to detail
Sensory - Must possess visual acuity and ability to effectively communicate
Benefits Include:
Highly competitive pay for travel professionals
Comprehensive medical, dental, and vision insurance with first day coverage
Paid Time Off (PTO) after 1560 hours
Life and Short-term disability offered
401(k) matching
Aggressive Refer-a-friend Bonus Program
24/7 recruiter support
Reimbursement for licensure and CEUs
Why Choose Fusion?
At Fusion Medical Staffing, our goal is to improve the lives of everyone we touch, and we're always looking for people like you to join our mission. Your passion for helping others deserves a partner just as committed to supporting you - that's why we offer day one insurance, $0 copay for mental health services, scholarships and awards, exclusive discounts, and more. From your personal recruiter to our clinical and traveler experience teams, we're here to guide and celebrate you along your journey. You take care of others; we take care of you.
Other Duties Disclaimer:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Other duties may be assigned. This job description is not a comprehensive list of all activities, duties, or responsibilities that are required of the employee for this job and is subject to change at any time with or without notice.
Start your rewarding career as a Travel Cath Lab Tech with Fusion Medical Staffing and join our mission to improve lives. Apply now!
*Fusion is an EOE/E-Verify Employer #pb10
Experienced Quality Technician
Quality assurance technician job in Chesterfield, MI
Quality
Technician
Auto-ApplyQuality Inspector/Tech
Quality assurance technician job in Roseville, MI
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
Quality Tech
Quality assurance technician job in Warren, MI
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.
Auto-ApplyQuality Assurance Specialist Intern - Summer 2026
Quality assurance technician job in Detroit, MI
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.
Manufacturing Technician (Operator)
Quality assurance technician job in Warren, MI
Dana is a global leader in the supply of highly engineered driveline, sealing, and thermal-management technologies that improve the efficiency and performance of vehicles with both conventional and alternative-energy powertrains. Serving three primary markets - passenger vehicle, commercial truck, and off-highway equipment - Dana provides the world's original-equipment manufacturers and the aftermarket with local product and service support through a network of nearly 100 engineering, manufacturing, and distribution facilities.
Current Starting Base Wage = $18.00
2nd & 3rd Shifts earn an additional $0.50 cents per hour for shift premium
JOB TITLE: Manufacturing Technician LOCATION: Production Warren
IMMEDIATE SUPERVISOR: Area Supervisor
POSITIONS SUPERVISED: N/A
GENERAL SUMMARY: Set-up, operate and maintain standard and complex manufacturing processes consistent with approved engineering standards and quality parameters. To be an active participant in line/cell teams, contribute to the company's vision and goals, while safely operating production equipment.
______________________________________________________________________
JOB RESPONSIBILITIES:
* 1. Operate equipment to accepted safety and production standards.
* 2. Maintain clean and safe work area utilizing 5S methodologies and in accordance with hazard assessment.
* 3. Actively participate in problem solving, continuous improvement and teaming activities utilizing the following methodologies:
* Use and maintain product and process controls utilizing Dynamic Control Plan (DCP) methodology.
* Participate in problem solving activities utilizing 8D and Poka-Yoke methodology.
* Strive for quality improvement and cost reduction, utilizing continuous improvement methodologies.
* Support in training and development of new team members.
* Work in and promote teamwork.
* 4. Maintain and utilize Statistical Process Control (SPC), Quality Operating System (QOS) measurables and all Dana reporting documentation.
* 5. Maintain and verify all quality gaging, Poka-Yokes and mistake proof devices in accordance with Dana engineered specifications.
* 6. Verify and maintain just-in-time inventory based on pull system.
* 7. Ensure that equipment is serviced as required utilizing Total Productive Maintenance (TPM) methodology.
* 8. Set-up all equipment in the entire cell to accepted engineering standards, utilizing quick changeover methodology.
* 9. Determine what repairs are required based on MRB documents.
* 10. Must be able to use hand gages, (micrometers, calipers, snap gages and master gages).
* 11. Notify supervisor of issues or problems.
* 12. DOT training if required Hilo driving.
* 13. Perform other duties as assigned by area supervisor.
KNOWLEDGE, SKILLS AND ABILITIES:
* 1. High school diploma, GED or equivalent work experience.
* 2. Must be willing to work in a team environment.
* 3. Ability to communicate effectively in both written and verbal form, as required.
* 4. Must have a positive attitude.
* 5. Must be willing to assume responsibility and be accountable for their actions.
* 6. Create and work in an environment of respect and integrity.
* 7. Helpful to be mechanically inclined.
* 8. Must have the ability to be trained in skills required per the training matrix.
* 9. Must be able to lift up to 50 pounds without a manipulator (lift assist).
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class.
Unsolicited Resumes from Third-Party Recruiters
Please note that as per Dana policy, we do not accept unsolicited resumes from third-party recruiters unless such recruiters were engaged to provide candidates for a specified opening. Any employment agency, person or entity that submits an unsolicited resume does so with the understanding that Dana will have the right to hire that applicant at its discretion without any fee owed to the submitting employment agency, person or entity.
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
Quality Assurance Associate - Pharmaceutical
Quality assurance technician job in Brighton, MI
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
Quality Assurance Associate - Pharmaceutical
Quality assurance technician job in Brighton, MI
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
Quality Technician - Injection Molding
Quality assurance technician job in Warren, MI
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
Auto-ApplyQuality Technician
Quality assurance technician job in Livonia, MI
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.
· Overtime varies depending on the needs of the business
Auto-ApplyQuality Technician
Quality assurance technician job in Livonia, MI
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.
· Overtime varies depending on the needs of the business
Auto-ApplyQuality Technician - Beverage (12 Hour Nights)
Quality assurance technician job in Westland, MI
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.
Auto-ApplyQuality Technician
Quality assurance technician job in Fraser, MI
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 ******************.
Easy ApplyQuality technician -$18 -Lake Orion
Quality assurance technician job in Lake Orion, MI
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 ************.
Quality Technician
Quality assurance technician job in Detroit, MI
Job DescriptionKey Responsibilities
Ensure error-proofing systems are active and not bypassed without approval
Issue and post Quality Alerts for customer-reported issues
Verify current End-of-Line (EOL) inspection processes are posted and followed
Perform product and workstation audits to ensure quality compliance
Track and report EOL defects using Excel
Audit reject tables and ensure supplier defects are properly tagged and placed in Quality Hold
Partner with SQEs and Production Supervisors to address customer concerns and maintain containment
Support Quality Engineers with root cause investigations and problem-solving
Qualifications
Associate degree in Quality, Engineering, or related field preferred (or equivalent experience)
Industry and product knowledge preferred; DMOS experience a plus
Strong problem-solving and communication skills
Proficiency in Microsoft Excel and basic computer applications
High attention to detail; ability to read prints/specifications a plus
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Quality Technician - 2nd Shift
Quality assurance technician job in Auburn Hills, MI
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
Auto-ApplyAutomotive Quality Technician
Quality assurance technician job in Sterling Heights, MI
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
Quality Technician
Quality assurance technician job in Sterling Heights, MI
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 **************.
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Quality Technician
Quality assurance technician job in Sterling Heights, MI
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 (2nd Shift)
Quality assurance technician job in Van Buren, MI
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)