What Jobs are available for Manufacturing Quality in the United States?

Job Description

Description:

Kronos has a long history of avionics engineering working with some of the largest aircraft integrators in the world. We always provide our partners with 100% customer satisfaction and on-time delivery. If you are excited about working for a company that takes its job seriously and does not cut corners you will have a home with Kronos.

Dictated pay rate: $45
Interviews: In person
Work Shift: 8am to 5 pm

Job Overview:
The FAIR Specialist is responsible for ensuring compliance with AS9102 standards for First Article Inspection Reports. This role entails detailed analysis of engineering documentation, materials, and components to assess their conformance to aerospace specifications and requirements. The ideal candidate will work closely with engineering and production teams to facilitate the initial stages of production while ensuring that quality assurance protocols are adhered to.

Key Responsibilities:
• Preparation and Review of FAIRs:
• Develop, prepare, and submit First Article Inspection Reports (FAIRs) in accordance with AS9102 guidelines.
• Review and analyze engineering drawings, specifications, and work instructions to ensure all data collected is accurate and complete.
• Stakeholder Collaboration:
• Collaborate with engineering and manufacturing teams to understand product specifications and requirements.
• Liaise with suppliers and vendors to gather necessary documentation and ensure compliance with supplier quality agreements.
• Inspection and Testing:
• Conduct detailed inspections, measurements, and tests on components as per AS9102 requirements to verify that all aspects of the design and manufacturing process meet industry standards.
• Document inspection results accurately and formulate corrective action plans for nonconformances.
• Compliance Monitoring:
• Ensure adherence to company quality management systems and AS9102 regulations throughout the inspection process.
• Perform audits and reviews of FAIR processes and documentation as needed.
• Continuous Improvement:
• Participate in root-cause analysis and problem-solving activities related to failed inspections or nonconformities.
• Recommend and implement process improvements to enhance quality and efficiency.

Qualifications:
• Education:
• Bachelor’s degree in Engineering, Quality Assurance, or a related field preferred.
• Experience:
• Minimum of 5 years of experience in aerospace quality assurance, particularly in First

Article Inspection processes.
• Demonstrated knowledge of AS9102 and aerospace standards.
• Skills:
• Proficient in reading and interpreting technical drawings and specifications.
• Strong analytical skills and attention to detail.
• Excellent communication and interpersonal skills.
• Familiarity with quality tools and methodologies (e.g., Six Sigma, Lean Manufacturing) is a plus.
• Certifications:
• AS9102 Auditor Certification is preferred.
• Quality Management System Auditing Certification (e.g., ISO 9001) is a plus

Kronos always provides our partners with 100% customer satisfaction and on time delivery. If you are excited about working for a company that takes its job seriously and does not cut corners you will have a home with Kronos.

Kronos always provides our partners with 100% customer satisfaction and on time delivery. If you are excited about working for a company that takes its job seriously and does not cut corners you will have a home with Kronos.

Job Description

Seeking Quality Manager for a tier 1 supplier of Automotive and Heavy Truck stamper. Must have knowledge of ISO and industry standards. Pay will be determined by qualifications. Business is up and we are working overtime and need qualified personnel to help run our quality department.

We can be reached through ZipRecruiter or you may also contact us by phone @ or by email @

Job Description

We are in need of Quality Manager to join our team!

GREAT PAY!

SAME WEEK PAY!

Key Responsibilities:

• Develop, implement, and maintain the company’s Quality Management System (QMS) in compliance with ISO standards.
• Lead internal and external audits , and ensure compliance with customer and regulatory requirements.
• Oversee in-process and final inspections , ensuring all products meet specifications.
• Manage corrective and preventive actions (CAPA) , root cause analysis, and continuous improvement initiatives.
• Collaborate with cross-functional teams to enhance product quality and reduce scrap, rework, and downtime.
• Serve as the primary contact for customer and supplier quality issues , complaints, and audits.
• Lead, mentor, and develop the quality team to maintain a culture of excellence.

Qualifications:

• Bachelor’s degree in Engineering, Manufacturing, or Quality Management (preferred).
• 5+ years of experience in quality within a manufacturing environment , including supervisory or management experience.
• Strong knowledge of ISO 9001 (and/or IATF 16949, ISO 13485, as applicable).
• Proficiency with quality tools and methodologies such as FMEA, SPC, PPAP, MSA, and Six Sigma .
• Excellent problem-solving, analytical, and leadership skills.
• CQE, CQM, or Six Sigma certification a plus.

Location of Job: Newberry, SC.

For immediate consideration, please respond to this posting with resume. Serious Inquiries Only.

LaborMax Staffing was founded in 2002. The company began with one office in Las Vegas, Nevada. Since its humble beginnings.

LaborMax has now grown to more than 70 branches in 20 states nationwide. Here at LaborMax, we are putting the focus back on building quality relationships between employers and employees. Whether it is a short or long term, we can take care of it. If you are an individual looking for work or a business searching for the right person for your workforce, then look no further than LaborMax Staffing to meet all of your staffing needs.

LaborMax Staffing was founded in 2002. The company began with one office in Las Vegas, Nevada. Since its humble beginnings.

LaborMax has now grown to more than 70 branches in 20 states nationwide. Here at LaborMax, we are putting the focus back on building quality relationships between employers and employees. Whether it is a short or long term, we can take care of it. If you are an individual looking for work or a business searching for the right person for your workforce, then look no further than LaborMax Staffing to meet all of your staffing needs.

Job Description

Manufacturing Quality Technician

Location-Charlotte-In person

Overview:

We are seeking a skilled and detail-oriented Manufacturing Quality Technician Electrical/Mechanical to ensure our products, systems, and processes meet customer, industry, and company quality standards. This role involves inspecting materials, mechanical components, and electrical systems, maintaining quality records, supporting continuous improvement initiatives, and ensuring compliance with safety and regulatory requirements in a manufacturing environment.

Key Responsibilities:

• Perform inspections on incoming materials, welds, in-process work, final products, and electrical systems to ensure compliance with drawings, blueprints, and industry standards.
• Install, maintain, and test electrical wiring, switchgear, motors, transformers, lighting, and other industrial electrical components.
• Conduct equipment testing for continuity, voltage, current, resistance, and mechanical tolerances.
• Maintain calibration records and manage non-conformance reports (NCRs).
• Collect, document, and report quality data for audits, projects, and process improvements.
• Support troubleshooting, corrective actions, and problem-solving for mechanical and electrical issues.
• Apply Non-Destructive Testing (NDT) methods such as MPI and LPI when required.
• Assist with ISO quality systems, including documentation, audits, and continuous improvement initiatives.
• Provide feedback to engineering teams regarding design improvements and document change requests.
• Occasionally maintain or modify basic PLC programs as required.
• Communicate effectively with cross-functional teams regarding quality issues and updates.
• Perform on-site installation, servicing, and warranty repairs for customer products.
• Maintain a clean, safe, and professional work environment in compliance with OSHA and safety standards.

Qualifications:

• Diploma in Mechanical, Electrical, or Industrial Technology (preferred).
• Licensed Journeyman or Industrial Electrician (for electrical responsibilities).
• 2–5+ years of experience in a manufacturing or industrial environment, preferably ISO-certified.
• Hands-on experience with AWS welding inspection and fabrication processes (mechanical) and industrial electrical systems .
• Knowledge of ISO 9001, AWS D1.1/CSA W47.1, AWS D1.1/W59, and NEC regulations.
• Basic PLC programming knowledge is a plus.
• Strong ability to read and interpret engineering drawings and schematics for both mechanical and electrical systems.
• Proficient in Microsoft Office and ERP systems.
• Ability to lift up to 50 lbs and travel across North America (valid passport & driver’s license required).

Skills & Attributes:

• Solid understanding of OSHA safety requirements and workplace safety.
• Strong problem-solving, organizational, and analytical skills .
• Effective communication skills and ability to work collaboratively with teams.
• Self-motivated, adaptable, and capable of multitasking in a fast-paced environment.
• Committed to delivering quality work on time and within budget .
• Maintains a clean, safe, and professional work environment .

Job Description

DUTIES AND RESPONSIBILITIES: FOOD Experienced

PLEASE DO NOT APPLY UNLESS YOU HAVE FOOD MANUFACTURING EXPERIENCE

• Food Safety Modernization Act trained
• Experience with: SOPS, GMPs, SSOP
• Certification in HACCP; HARPC

Manager for all aspects of food manufacturing, to include coordinating daily tasks, Sanitation, Food Safety audits;

▪ Ensure that all of the quality check procedures put in place by the company are followed during

every production phase of food manufacturing

QUALIFICATIONS:

▪ 2-3 years of experience as a Quality Control Inspector in food industry.

▪ High School Diploma/GED required.

▪ Industry certifications

▪ Able to developed protocols in English and Spanish

▪ Ability to work in a team environment; excellent communication skills.

• Bilingual English/Spanish

▪ Computer skills (word, Excel, PowerPoint)

▪ Ability to enforce processes and control conformance.

▪ Ability to develop and implement process controls for product safety and quality.

▪ Strong understanding industry of raw materials and the manufacturing industry.

▪ Open to working night

Contribute to the growth and success of the company. If you're ready to be part of an exciting and growing company, apply now!

Contribute to the growth and success of the company. If you're ready to be part of an exciting and growing company, apply now!

Job Description

Located in Bristol, Rhode Island for over 50 years, Tri-Mack is a leading manufacturer of high-temperature thermoplastic components for the aerospace-defense, semiconductor, energy and medical industries. 

Our broad capabilities include collaborative engineering, tool making, injection molding, thermoplastic composite processing, multi-axis CNC machining, bonding and assembly, testing and quality control - all within a modern, environmentally controlled 60,000 sq. ft. facility. 

Our culture is based on values that promote respect, teamwork and accountability and we are committed to meeting customer requirements through our ISO 9001/AS9100 quality management system. 

PLEASE NOTE - Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

Position: Quality Engineer

Summary: 

The Quality Engineer is responsible for the measurement systems development and data analysis with the objective of improving Tri-Mack process consistency and product quality.  This position engages in new product / process development and legacy process improvement.  New process work includes measurement system development, collaborative process assessment and development as well as process substantiation documentation.  Legacy products and processes are supported with efforts to improve measurement systems, process consistency and product conformance.  This position reports to the Quality Manager.

Responsibilities & Accountabilities:

New Product Development

• Measurement System development and analysis to AS13003 and/or customer requirements.
• Direct collaborative PFMEA development to AS13004 and/or customer requirements.
• Collaboratively develop process control plans to meet AS13006, AS13002, and/or customer requirements.
• Develop CMM programs, fixture design, and operation instructions as required.
• Prepare FAI, PPAP, and AQPQ documents and packages and other process substantiation as required.

Legacy Product Support

• Retrospective process and product analysis as identified in the New Product Development section above.
• Inspect and test materials, equipment, processes and products.
• Perform process capability assessments as requested.
• Employ Design of Experiments, Quality Function Deployment, Process Mapping, Statistical analysis and other tools to facilitate process improvement.
• Provide In-process Inspection support and expertise as required.
• Develop process control plan improvements as requested.
• Lead collaborative RCCA efforts as required.
• Evaluate Tri-Mack Quality standards, controls, specifications and processes.  Recommend and implement improvements.
• Analyze Company quality data and propose improvement methods.

General

• Support Tri-Mack, AS9100, NADCAP, customer and regulatory system conformance.
• Support quality initiatives, other projects and assignments as directed by the Quality Manager.
• Maintain a clean and orderly work area.
• Demonstrate the Tri-Mack values of Respect, Integrity, Accountability, Teamwork and Durability at all times.

Education, Skills & Experience:

• Associates in Engineering; Bachelors in Engineering preferred
• Experience in a manufacturing environment
• Experience with CAD design, SolidWorks preferred
• Proficiency with Microsoft Office Suite required
• Familiarity with quality control systems and protocol required
• Demonstrated blueprint interpretation, GD&T experience preferred
• Some experience with Lean and/or Six-Sigma preferred
• Strong written and oral communication skills
• Excellent organizational skills and attention to detail, analytical and problem-solving skills.
• Time management skills with a proven ability to meet deadlines.
• Flexible, work with a high sense of urgency, and able to get along well with others.

Our Benefits:

We offer competitive salaries and generous benefits, including:

• 40-hour, Monday-Friday schedule
• Medical, Life & Dental Insurance
• Paid Holiday, Personal Time & Vacation
• 401(k) with Company Match
• Tuition Reimbursement

If you’re looking for an innovative,  values-driven company where you can put your engineering aptitude and quality expertise to work, grow your career and take on ever-bigger challenges, you may just have found the place! We know our continued success is dependent upon our employees, which is why we are always on the lookout for reliable, knowledgeable and dynamic individuals with past success in a collaborative team setting, working with clear objectives and direction.

*Tri-Mack Plastics provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status or genetic information. Tri-Mack is a drug-free work environment. Pre-employment drug screening (excludes THC) and background checks are required.

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Job Description

Job Title: Manufacturing Quality Specialist
Job Description

We are seeking a Quality Assurance Associate to support a major pharmaceutical client. The QA Associate will be responsible for real-time batch record review on the manufacturing shop floor, ensuring compliance and accuracy in documentation.

Responsibilities

• Execute real-time review of batch documentation and other manufacturing documentation, analyzing for errors, corrections, and compliance.
• Perform housekeeping and GMP walkthroughs of the facility.
• Initiate and participate in triage for on-the-floor events.
• Work in cross-functional teams to meet and exceed timelines.
• Execute or review room and line clearances.
• Make quality decisions in real-time according to regulations ICH Q7 and 21CFR211, as well as internal procedures.

• Experience in batch record review.
• Good Manufacturing Practice (GMP) experience in a manufacturing facility.
• Quality assurance experience in the pharmaceutical industry for at least 6 months.

• Exposure to different complex manufacturing processes such as vaccines and monoclonal antibodies (mAbs).
• Experience in starting new teams critical to site performance.
• Opportunities for advancement into higher-level roles.

This role operates on the 2nd shift from 3 PM to 11:30 PM. Occasional overtime may be needed based on business needs, with weekend work opportunities highly encouraged. The job requires presence on the pharma manufacturing floor and office space with a desk, but it is not an office-based role. Expectation is to be on the shop floor 90-100% of the shift. Dress code is business casual with closed-toed shoes, and adherence to aseptic gowning procedures is required.

Job Type & Location

This is a Contract position based out of Sanford, North Carolina.

Pay and Benefits

The pay range for this position is $35.00 - $45.00/hr.

Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending

Job Description

Top Job

Located in Cincinnati, OH

Salary: $22-25 an hour

Specialized Recruiting Group is seeking a Manufacturing Quality Control Technician on 1st shift for a Direct Hire opening in Woodlawn, OH!

Responsibilities:

• Inspect using measuring instruments as needed.
• Investigate and recreate reported defects.
• Work with other employees to troubleshoot and resolve coding issues.
• Track and document all testing defects and resolutions.
• Interpret blueprints on the shop floor as needed.

• Previous experience with Quality is required.
• Previous experience in the Manufacturing Industry is required.
• CMM experience is a plus.
• Ability to read blueprints.
• NDT experience is a plus
• Must have experience with gauges, micrometers, and calipers.
• Knowledge of GD&T.

Job Description

Job Title: Manufacturing Quality Specialist

Job Description

We are seeking a Quality Assurance Associate to support a major pharmaceutical client. The QA Associate will be responsible for real-time batch record review on the manufacturing shop floor, ensuring compliance and accuracy in documentation.

Responsibilities

• Execute real-time review of batch documentation and other manufacturing documentation, analyzing for errors, corrections, and compliance.
• Perform housekeeping and GMP walkthroughs of the facility.
• Initiate and participate in triage for on-the-floor events.
• Work in cross-functional teams to meet and exceed timelines.
• Execute or review room and line clearances.
• Make quality decisions in real-time according to regulations ICH Q7 and 21CFR211, as well as internal procedures.

Essential Skills

• Experience in batch record review.
• Good Manufacturing Practice (GMP) experience in a manufacturing facility.
• Quality assurance experience in the pharmaceutical industry for at least 6 months.

Additional Skills & Qualifications

• Exposure to different complex manufacturing processes such as vaccines and monoclonal antibodies (mAbs).
• Experience in starting new teams critical to site performance.
• Opportunities for advancement into higher-level roles.

Job Type & Location

This is a Contract position based out of Sanford, NC.

Pay and Benefits

The pay range for this position is $35.00 - $45.00/hr.

Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending