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Cqa Jobs in Indiana (NOW HIRING)

ASQ CSQP, CQE, CQA, or Lean Six Sigma Green Belt. * Demonstrated success with supplier audits, corrective actions, and development initiatives. Work Environment & Physical Requirements This role ...

Master's degree or professional certification (CQE, CQA, Six Sigma Black Belt) preferred Experience and qualifications * Typically, 7 or more years of progressive experience in quality assurance ...

ASQ Certifications (CQA, CQI, CQT) * Manufacturing or machine shop experience General Applicable Company Competencies * Commitment to Watts' values of integrity, accountability, continuous ...

Quality Engineer

Michigan City, IN · On-site

$70K - $90K/yr

ASQ certifications such as CQE, CQA, or CQM, prefered * Hands-on experience with Lean and Six Sigma tools (e.g., Value Stream Mapping, Root Cause Analysis, Cpk/Ppk, GR&R, Kaizen, 5S). * Knowledge of ...

Certifications such as ASQ CSQP, CQE, CQA, or Lean Six Sigma Green Belt are strongly preferred. * Demonstrated success in supplier audits, corrective action management, and supplier development.

Certified Quality Engineer (CQE), Certified Quality Auditor (CQA), or ISO 9001:2015 Internal Auditor Certification preferred * Strong knowledge of ISO 9001:2015 and/or IATF 16949 Quality Management ...

ASQ Certifications (CQA, CQI, CQT) * Manufacturing or machine shop experience General Applicable Company Competencies * Commitment to Watts' values of integrity, accountability, continuous ...

Showing results 41-59

Cqa information

See Indiana salary details

$14

$35

$65

How much do cqa jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for cqa in Indiana is $35.60, according to ZipRecruiter salary data. Most workers in this role earn between $27.45 and $39.81 per hour, depending on experience, location, and employer.

What is a Certified Quality Auditor?

CQA professionals, or Certified Quality Auditors, are individuals certified to examine and evaluate the quality systems of organizations. They assess processes, products, and systems to ensure compliance with established standards and identify areas for improvement. CQAs use auditing techniques to verify effectiveness and recommend corrective actions, playing a vital role in maintaining and enhancing quality within a company. Their expertise is recognized across industries, including manufacturing, healthcare, and services.

What are the key skills and qualifications needed to thrive as a Certified Quality Auditor?

To thrive as a Certified Quality Auditor (CQA), you need a solid understanding of quality management principles, audit processes, and industry regulations, typically supported by a CQA certification from organizations like ASQ. Familiarity with audit management software, data analysis tools, and standards such as ISO 9001 is essential. Strong attention to detail, analytical thinking, and effective communication skills help auditors identify issues and clearly present findings. These capabilities are crucial for ensuring organizational compliance, driving continuous improvement, and maintaining high standards of quality.

What are some common challenges faced by a Certified Quality Auditor and how can they be addressed?

A CQA professional often encounters challenges such as staying updated with frequently changing regulatory requirements, managing complex documentation, and ensuring consistent compliance across multiple clinical sites. Addressing these challenges requires continuous professional development, effective communication with cross-functional teams, and strong organizational skills. Building collaborative relationships with clinical operations and regularly participating in training sessions can help CQA professionals navigate evolving standards and maintain high-quality assurance practices.

What is the difference between Cqa vs Quality Assurance Specialist?

AspectCqaQuality Assurance Specialist
CertificationsISO 9001, Six Sigma, CQEISO 9001, Six Sigma, CQE
Work EnvironmentManufacturing, Pharmaceutical, Medical DevicesSoftware, Manufacturing, Healthcare
Employer & Industry UsageManufacturing, Medical Devices, PharmaTech, Manufacturing, Healthcare

Both Cqa (Certified Quality Auditor) and Quality Assurance Specialist roles focus on quality management, with overlapping certifications like ISO 9001 and Six Sigma. Cqas typically work in manufacturing, medical devices, and pharmaceutical industries, conducting audits and ensuring compliance. Quality Assurance Specialists often work across various sectors including software and healthcare, focusing on process improvement and product quality. While their environments differ, both roles aim to uphold quality standards and require similar credentials.

What are popular job titles related to Cqa jobs in Indiana?

For Cqa jobs in Indiana, the most frequently searched job titles are:

Infographic showing various Cqa job openings in Indiana as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $74,048 per year, or $35.6 per hour.

Supplier Quality Engineering Lead

Amaco

Indianapolis, IN • On-site

$85K - $110K/yr

Other

Posted 9 days ago


Job description

About AMACO

Since 1919, American Art Clay Company (AMACO) has helped makers, schools, and studios bring ideas to life. As a fourth-generation, family-owned manufacturer, we pioneered lead-free glazes, electric kilns, potter’s wheels, and both ceramic and non-ceramic clays. A founding member of the Arts and Creative Materials Institute, we’ve championed product safety standards for nearly a century. Our culture is rooted in continuous improvement, curiosity, and craftsmanship—where every voice can influence safety, quality, customer care, teamwork, and learning.

The Role

Reports to: Director of Operations

As our Supplier Quality Engineering Lead, you’ll architect and run the supplier quality ecosystem that ensures every incoming component and raw material meets AMACO and Brent standards. Picture this: you start your day reviewing incoming inspection trends, then jump into a root-cause session with a supplier, and finish by coaching your team on CTQ test methods. You’ll be the bridge between production, procurement, and engineering—solving problems fast and building supplier partnerships that last.

What You’ll Lead
  • Program design: Build and maintain supplier qualification, auditing, monitoring, and scorecard systems. Define incoming inspection plans and train teams (internal and external) on CTQ methods.
  • Rapid discrepancy response: Be first on the scene when issues arise. Drive investigations, lead 8D/root-cause analyses, implement corrective actions, and loop in the In-Process Quality Supervisor when process fixes are needed.
  • Cross-functional collaboration: Partner with production to keep lines running, and with procurement/engineering on supplier selection and development.
  • Continuous improvement: Deploy AMACO and Brent Quality System standards with suppliers. Lead corrective action systems, Kaizen events, and A3 problem-solving focused on supplier performance.
Your Team
  • Directly manage supplier quality staff—set objectives, plan schedules, and conduct performance reviews.
  • Be a hands-on coach, mentoring the team in quality fundamentals and the unique characteristics of ceramics.
How Success Is Measured
  • Fewer supplier-caused defects and incoming inspection failures.
  • Less production downtime linked to supplier quality.
  • Rising supplier scorecard results across defects, delivery, and compliance.
  • Corrective actions that are timely, effective, and sustained.
Core Capabilities
  • Fluency in test methods, auditing, and supplier quality frameworks.
  • Applied experience with CTQs, PPAP, FMEA, and 8D.
  • Influence-first leadership and strong supplier negotiation.
  • Practical judgment balancing quality, cost, and delivery.
  • Project planning, organization, and crisp communication.
Qualifications
  • Bachelor’s in Ceramics, Engineering, Materials Science, Industrial Technology, or similar. (Associate’s plus significant relevant experience considered.)
  • 5–7+ years in supplier quality or quality engineering within manufacturing.
  • Proven track record establishing a Supplier Quality System.
  • ISO 9001 proficiency; exposure to IATF 16949, AS9100, or ISO 13485 is a plus.
  • SPC/statistical analysis skills (Minitab preferred).
  • History of developing and documenting quality standards, including converting attribute criteria to numeric specifications.
  • Preferred credentials: ASQ CSQP, CQE, CQA, or Lean Six Sigma Green Belt.
  • Demonstrated success with supplier audits, corrective actions, and development initiatives.
Work Environment & Physical Requirements

This role involves extended standing and lifting/heavy lifting. Ability to work in both hot and cold environments is required.

Physical Demands: Regular talking and hearing; frequent standing, walking, hand use, and reaching; occasional sitting, climbing/balancing, and stooping/kneeling/crouching/crawling. Frequent lifting/moving of up to 50+ pounds. Vision needs include close, distance, color, peripheral, depth perception, and focus adjustment.

Schedule & Travel

Position Type/Hours: Full-time, Monday–Friday, 40+ hours per week, with occasional evenings/weekends as needed.

Travel: Up to 30%.

Inclusion & Accessibility

Reasonable accommodations may be made to enable individuals with disabilities.

EEO Statement:

AMACO is an Equal Opportunity Employer and Prohibits Discrimination and Harassment of Any Kind: AMACO is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at AMACO are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the location where we operate. AMACO will not tolerate discrimination or harassment based on any of these characteristics.

Other Notes

Duties and responsibilities may evolve as the business grows; flexibility to take on related tasks is expected.

Preferred Proficiencies
  • Quality inspection
  • Continuous improvement (Kaizen)
  • Troubleshooting complex quality issues
  • APQP
  • Supplier relationship management
  • Writing and maintaining SOPs
  • Quality control and data analysis