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AAON, Inc.

Quality Engineer II

Memphis, TN

$69K - $90K/yr

Working knowledge of ISO 9001 QMS, internal auditing, and nonconforming material/CAPA processes Certified Quality Process Analyst (CQPA) or ASQ Certified Quality Engineer (CQE) Preferred * Data ...

AAON, Inc.

Quality Engineer II

Memphis, TN · On-site

$69K - $90K/yr

Working knowledge of ISO 9001 QMS, internal auditing, and non-conforming material/CAPA processes Certified Quality Process Analyst (CQPA) or ASQ Certified Quality Engineer (CQE) Preferred * Data ...

Flex Ltd.

CoPQ Quality Technician

Columbia, SC · On-site

$16.75 - $22.50/hr

ASQ certification as CQT, CQA, CQPA or CSSGB is desired. ISO 9000, ESD, OSHAS 18000, ISO 14001 is preferred but not required. KD07 What you'll receive for the great work you provide: * Full range of ...

Flex

CoPQ Quality Technician

Columbia, SC

$16.75 - $22.50/hr

ASQ certification as CQT, CQA, CQPA or CSSGB is desired. ISO9000, ESD, OSHAS 18000, ISO 14001 is preferred but not required. KD07 What you'll receive for the great work you provide: * Full range of ...

VOLT

Quality Technician 3 | 1st Shift

Milpitas, CA · On-site

$30/hr

ASQ certification as CQT, CQA, CQPA or CSSGB is desired * Occasionally lift and/or move up to 25 pounds * Ability to handle small components Pay rate: $30.00 per hour *Pay range offered to a ...

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Cqpa information

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$14

$36

$55

How much do cqpa jobs pay per hour?

As of Jun 9, 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 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.

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.
More about Cqpa jobs
What cities are hiring for Cqpa jobs? Cities with the most Cqpa job openings:
What states have the most Cqpa jobs? States with the most job openings for Cqpa jobs include:
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Cqpa jobs near you
Infographic showing various Cqpa job openings in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 81% In-person, and 19% Remote job distribution, with an average salary of $74,936 per year, or $36 per hour.
QA Specialist II

QA Specialist II

Astrix Inc

Vista, CA • On-site

$35 - $52/hr

Full-time

Posted 22 days ago

Job description

Our client a leading biotech company is looking for a skilled QA Specialist to join their team in San Diego County, CA!
Job Title: QA Specialist
Pay rate: $35/hr. - $52/hr. DOE
Job type: Contract- hire
Location: San Diego County, CA
Overview
The QA Specialist II is responsible for supporting day-to-day Quality Assurance operations within a GMP-regulated pharmaceutical manufacturing environment. This role ensures that drug substances manufactured meet FDA, EU, and other applicable regulatory requirements for research, pre-clinical, clinical, and commercial use. The position focuses on GMP documentation control, quality system oversight, and support of internal and external audits.
Key Responsibilities
  • Perform production room, dispensary, and shipment clearance verifications as required.
  • Review, revise, and maintain Standard Operating Procedures (SOPs) and other GMP-controlled documents such as stability protocols, raw material specifications, and environmental monitoring trend reports.
  • Manage GMP documentation workflows, including reconciliation, issuance, review, and archival of records.
  • Verify accuracy of scanned batch production records (BPRs), chromatograms, and other GMP documents, ensuring proper labeling, boxing, and archiving.
  • Coordinate, review, and approve quality events and associated documentation.
  • Support internal, customer, and regulatory audits by providing required documentation and QA guidance.
  • Provide cGMP guidance to manufacturing and cross-functional departments.
  • Participate in continuous improvement initiatives and represent QA in cross-functional project teams.
  • Implement and maintain Quality Management System (QMS) processes and standards.
  • Scan, verify, and archive GMP records in compliance with internal procedures.
  • Support system and process harmonization initiatives across sites and electronic quality systems (e.g., MasterControl).
Qualifications
  • Bachelor's degree in a science-related field required; Master's or Ph.D. preferred.
  • 3-5 years of experience in Quality Assurance, Quality Control, or GMP manufacturing environment required.
  • Experience working in ISO 7 and ISO 8 controlled environments preferred.
  • Knowledge of FDA regulations, cGMP, GxP, and Quality Management Systems required.
  • Experience with internal audits and regulatory inspections required.
  • Strong ability to review GMP documents (including BPRs and chromatograms) with high accuracy.
  • Proficiency in Microsoft Office (Word, Excel, PowerPoint) and electronic document management systems.
  • Strong organizational, multitasking, and time-management skills in a fast-paced environment.
  • Ability to work independently and collaboratively in cross-functional teams.
  • Problem-solving ability and attention to detail essential.
  • Preferred certifications: ASQ Certified Quality Auditor (CQA), Certified Quality Engineer (CQE), or Certified Quality Process Analyst (CQPA).
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