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Aaon Coil Products Inc.

Quality Engineer II

Memphis, TN · On-site

$70 - $90/hr

ISO 9001** QMS, internal auditing, and non‐conforming material/CAPA processes Certified Quality Process Analyst (CQPA) or ASQ Certified Quality Engineer (CQE) Preferred* **Data & Software:

ConnectiveRx

Sr. Quality Management Specialist

Whippany, NJ · On-site

$54K - $106K/yr

... CQPA), Supplier Quality (CSQP), ISO9001:2015 Auditor or equivalent(s). Compensation & Benefits: This position offers opportunities for a bonus (or commissions), with total compensation varying based ...

ConnectiveRx

Sr. Quality Management Specialist

Whippany, NJ

$83K - $114K/yr

... CQPA), Supplier Quality (CSQP), ISO9001:2015 Auditor or equivalent(s). Compensation & Benefits: This position offers opportunities for a bonus (or commissions), with total compensation varying based ...

Quality Technology Services, LLC

American Society for Quality (ASQ) certified CMQ/OE, CQIA, CQPA, CQE, and/or CQA * Experience with delivery of mission critical data center facilities. * Experience working with MEP trades. TOTAL ...

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Cqpa information

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$14

$36

$55

How much do cqpa jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for cqpa in the United States is $36.03, according to ZipRecruiter salary data. Most workers in this role earn between $27.88 and $41.83 per hour, depending on experience, location, and employer.

What is a CQPA?

A CQPA, or Certified Quality Process Analyst, is a professional who is trained to evaluate and improve processes within an organization, ensuring quality standards are met. They collect and analyze data, solve process-related problems, and support continuous improvement initiatives. Typically, CQPAs work alongside quality engineers and managers to help their organizations maintain high-quality products and services. The certification is offered by the American Society for Quality (ASQ) and demonstrates a foundational understanding of quality tools and techniques.

What are some common challenges faced by a Certified Quality Process Analyst (CQPA) when working on cross-functional teams?

As a CQPA, one of the common challenges when working with cross-functional teams is aligning diverse perspectives and priorities toward shared quality objectives. You may need to bridge communication gaps between departments such as engineering, production, and management, ensuring that quality improvement initiatives are understood and supported by all stakeholders. Additionally, balancing data-driven analysis with practical constraints on the shop floor can require flexibility and strong interpersonal skills. Overcoming resistance to process changes and maintaining consistent documentation are also frequent hurdles, but they provide valuable opportunities to develop leadership and problem-solving abilities.

What are the key skills and qualifications needed to thrive as a Clinical Quality Program Administrator (CQPA), and why are they important?

To thrive as a Clinical Quality Program Administrator (CQPA), you need expertise in healthcare quality management, data analysis, and a relevant degree in healthcare administration or a related field. Familiarity with quality improvement methodologies, accreditation standards, and tools such as Six Sigma, Lean, or quality reporting systems is typically required. Strong communication, leadership, and problem-solving skills help you collaborate effectively across departments and drive quality initiatives. These skills ensure the delivery of safe, high-quality patient care and regulatory compliance within healthcare organizations.

What is the difference between Cqpa vs Cphq?

AspectCqpaCphq
CertificationsCertified Quality Process Analyst (CQPA)Certified Professional in Healthcare Quality (CPHQ)
Work EnvironmentQuality assurance, process improvement, manufacturing, and industrial settingsHealthcare quality management, patient safety, healthcare organizations
Industry UsageManufacturing, industrial, and business sectorsHealthcare industry, hospitals, clinics
CredentialsFocuses on quality processes and analysisFocuses on healthcare quality and patient safety

The main difference between Cqpa and Cphq lies in their industry focus and certification content. Cqpa is geared towards quality process analysis in manufacturing and industrial sectors, while Cphq is specialized for healthcare quality management and patient safety. Both certifications emphasize quality improvement but serve different professional environments.

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Cqpa jobs near you
Infographic showing various Cqpa job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 80% In-person, and 20% Remote job distribution, with an average salary of $74,936 per year, or $36 per hour.

Senior Manager-Global Quality Systems

Cooper Companies

Trumbull, CT • On-site

Full-time

Posted 18 days ago

Job description

Scope: 

The Senior Manager, Global Quality Systems provides leadership and oversight for key elements of CooperSurgical's Global Quality Management System (QMS), including Management Review, Quality System Metrics and Reporting, Regulatory Intelligence, Quality System Impact Assessments, and Quality System integration activities associated with acquisitions and strategic business initiatives. Partners closely with Quality, Regulatory Affairs, Operations, Manufacturing, R&D, Supply Chain, IT, and other functional leaders to ensure QMS remains compliant, effective, scalable, and aligned with evolving regulatory requirements and business objectives.  Serves as a key partner to the Director, Global Quality Systems, helping drive quality system performance, governance, inspection readiness, and continuous improvement across the global organization.

Qualifications

Knowledge, Skills and Abilities:

Required

  • Strong working knowledge of MasterControl, Veeva, Trackwise, or similar eQMS platforms. 
  • Solid understanding of 21 CFR 820, ISO 13485, EU MDR, MDSAP. 
  • Demonstrated ability to manage and develop teams. 
  • Ability to balance operational priorities with compliance requirements. 
  • Strong organizational, analytical, and communication skills. 
  • Ability to collaborate across global, crossfunctional groups.

Preferred

  • Experience participating in or supporting large-scale enterprise software implementations, including data migration and data mapping activities.
  • Advanced proficiency in Excel for data analysis and reporting.
  • Professional certification such as Certified Quality Auditor (CQA) or similar.

Work Environment:

  • Standard office environment with regular use of computer systems and virtual collaboration tools. 

Experience:

Required

  • 8+ years of experience in quality management systems, within a regulated med tech industry.
  • 7+ years of people leadership and team development.
  • Experience managing quality systems with ISO 13485 and FDA 21 CFR Part 820, MDSAP, and EU MDR requirements.

Preferred

  • Exposure to other adjacent quality system compliance requirements such as 21 CFR Part 210/211.
  • Prior involvement in supporting external and internal audits.
  • Experience with electronic Quality Management Systems (eQMS) and/or implementation of eQMS, such as Veeva, Trackwise, MasterControl.

Education:

Required

  • Bachelor's degree in a relevant field such as Engineering, Life Sciences, Quality, or a related discipline.

Preferred

  • Professional ASQ certification (CQPA, CQA, CMQ/OE, etc.)
  • Project Management Professional certification (PMP)

Qualifications

Knowledge, Skills and Abilities:

Required

  • Strong working knowledge of MasterControl, Veeva, Trackwise, or similar eQMS platforms. 
  • Solid understanding of 21 CFR 820, ISO 13485, EU MDR, MDSAP. 
  • Demonstrated ability to manage and develop teams. 
  • Ability to balance operational priorities with compliance requirements. 
  • Strong organizational, analytical, and communication skills. 
  • Ability to collaborate across global, crossfunctional groups.

Preferred

  • Experience participating in or supporting large-scale enterprise software implementations, including data migration and data mapping activities.
  • Advanced proficiency in Excel for data analysis and reporting.
  • Professional certification such as Certified Quality Auditor (CQA) or similar.

Work Environment:

  • Standard office environment with regular use of computer systems and virtual collaboration tools. 

Experience:

Required

  • 8+ years of experience in quality management systems, within a regulated med tech industry.
  • 7+ years of people leadership and team development.
  • Experience managing quality systems with ISO 13485 and FDA 21 CFR Part 820, MDSAP, and EU MDR requirements.

Preferred

  • Exposure to other adjacent quality system compliance requirements such as 21 CFR Part 210/211.
  • Prior involvement in supporting external and internal audits.
  • Experience with electronic Quality Management Systems (eQMS) and/or implementation of eQMS, such as Veeva, Trackwise, MasterControl.

Education:

Required

  • Bachelor's degree in a relevant field such as Engineering, Life Sciences, Quality, or a related discipline.

Preferred

  • Professional ASQ certification (CQPA, CQA, CMQ/OE, etc.)
  • Project Management Professional certification (PMP)

Essential Functions & Accountabilities:

  • Support the governance, effectiveness, and continuous improvement of the global QMS.
  • Drive harmonization, compliance, and operational excellence across global quality system processes. 
  • Partner with process owners and cross-functional stakeholders to identify and mitigate quality system risks while ensuring inspection readiness.
  • Lead the global Management Review program, including planning, reporting, action tracking, and continuous improvement. 
  • Develop and maintain quality system KPIs, dashboards, and performance reporting to provide visibility into QMS effectiveness, compliance status, and emerging risks. 
  • Prepare executive-level reporting on QMS health, quality objectives, risks, and improvement opportunities.
  • Monitor process effectiveness and drive improvements that enhance compliance, efficiency, and user experience.
  • Monitor evolving global regulations, standards, guidance documents, and industry best practices impacting the Quality Management System. 
  • Lead quality system impact assessments and gap analyses to determine the effect of regulatory and standards changes on existing QMS processes.
  • Develop and track implementation plans to ensure timely incorporation of regulatory and standards requirements into the QMS.
  • Partner with Regulatory Affairs and Quality leadership to evaluate new or revised regulatory requirements.
  • Lead Quality Systems due diligence, integration planning, and QMS harmonization activities associated with acquisitions and strategic business initiatives. 
  • Assess quality system maturity, identify compliance gaps, and implement integration plans that align acquired entities with CooperSurgical processes. 
  • Support implementation and optimization of electronic Quality Management Systems (eQMS) and related quality system enhancement initiatives.
  • Support regulatory inspections, audits, and remediation activities as required.
  • Lead, coach, and develop a team responsible for Quality Systems governance, reporting, compliance monitoring, and improvement initiatives.
  • Establish performance expectations, prioritize resources, and foster a culture of quality, accountability, and continuous improvement.

Travel: 

This position may require 20% domestic or international travel. 

Job Summary:

The Senior Manager, Global Quality Systems is responsible for the leadership, oversight, and continuous improvement of key components of CooperSurgical's Global Quality Management System. This role ensures ongoing compliance with applicable global regulations and standards, including FDA QMSR, ISO 13485, MDSAP, EU MDR, and other relevant requirements.  Leads activities related to Management Review, Quality System metrics and reporting, regulatory intelligence, standards management, quality system impact assessments, and merger and acquisition integration efforts. Through effective governance, analytics, and cross-functional collaboration, this role provides visibility into QMS health, identifies compliance risks and opportunities, and ensures regulatory and standards changes are effectively assessed and incorporated into the Quality Management System.

Essential Functions & Accountabilities:

  • Support the governance, effectiveness, and continuous improvement of the global QMS.
  • Drive harmonization, compliance, and operational excellence across global quality system processes. 
  • Partner with process owners and cross-functional stakeholders to identify and mitigate quality system risks while ensuring inspection readiness.
  • Lead the global Management Review program, including planning, reporting, action tracking, and continuous improvement. 
  • Develop and maintain quality system KPIs, dashboards, and performance reporting to provide visibility into QMS effectiveness, compliance status, and emerging risks. 
  • Prepare executive-level reporting on QMS health, quality objectives, risks, and improvement opportunities.
  • Monitor process effectiveness and drive improvements that enhance compliance, efficiency, and user experience.
  • Monitor evolving global regulations, standards, guidance documents, and industry best practices impacting the Quality Management System. 
  • Lead quality system impact assessments and gap analyses to determine the effect of regulatory and standards changes on existing QMS processes.
  • Develop and track implementation plans to ensure timely incorporation of regulatory and standards requirements into the QMS.
  • Partner with Regulatory Affairs and Quality leadership to evaluate new or revised regulatory requirements.
  • Lead Quality Systems due diligence, integration planning, and QMS harmonization activities associated with acquisitions and strategic business initiatives. 
  • Assess quality system maturity, identify compliance gaps, and implement integration plans that align acquired entities with CooperSurgical processes. 
  • Support implementation and optimization of electronic Quality Management Systems (eQMS) and related quality system enhancement initiatives.
  • Support regulatory inspections, audits, and remediation activities as required.
  • Lead, coach, and develop a team responsible for Quality Systems governance, reporting, compliance monitoring, and improvement initiatives.

  • Establish performance expectations, prioritize resources, and foster a culture of quality, accountability, and continuous improvement.

    Travel: This position may require 20% domestic or international travel. 

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