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Full Time Asq Cqa Jobs (NOW HIRING)

CGI INC.

Quality Assurance Technician

Aberdeen, MD

$139K/yr

J0726-0840 Employment Type: Full Time Position Description: CGI Federal is seeking a Quality ... ASQ certifications (CQI, CQA, CQE) . IPC inspection certifications (if electronics related ...

CGI Inc.

Quality Assurance Technician

Aberdeen, MD · On-site

J0726-0840 Employment Type: Full Time Position Description: CGI Federal is seeking a Quality ... ASQ certifications (CQI, CQA, CQE) . IPC inspection certifications (if electronics related ...

Systimmune

Quality Assurance Manager

Redmond, WA · On-site

$120K - $160K/yr

This position is full-time onsite in Redmond, WA and will transition to our new Bothell, WA ... ASQ certification (e.g., CQA) is a plus Key Competencies * Strong understanding of bioanalytical QA ...

Treske Precision Machining

Quality Engineer

Sherwood, OR

$77K - $100K/yr

... OR | Full-Time, On-Site Treske Precision Machining, Inc. is a precision machine shop. We serve ... ASQ Certified Quality Engineer (CQE) or Certified Quality Auditor (CQA). * Lean Six Sigma Green ...

BAE Systems

Quality Manager I

Aiken, SC · On-site

$92K - $156K/yr

ASQ Certification (CQE, CQA, or CMQ/OE). * Extensive experience supporting quality operations in a ... Pay Information Full-Time Salary Range: $92180 - $156707 Please note: This range is based on our ...

SystImmune, Inc

Quality Assurance Manager

Redmond, WA · On-site

$120K - $160K/yr

This position is full-time onsite in Redmond, WA and will transition to our new Bothell, WA ... ASQ certification (e.g., CQA) is a plus Key Competencies * Strong understanding of bioanalytical QA ...

HII

Quality Manager (Mgr Quality 2) - 28646

Alma, MI · On-site

$102K - $124K/yr

Requisition Number: 28646 Required Travel: 26 - 50% Employment Type: Full Time/Salaried/Exempt ... Certifications such as ASQ CQE, CQA, Six Sigma Green/Black Belt, or equivalent. Physical ...

Hitachi

Quality Engineer

Michigan City, IN · On-site

$70K - $90K/yr

Engineering & Science Job Schedule: Full time Remote: No Hitachi Global Air Power: We build the ... ASQ certifications such as CQE, CQA, or CQM, prefered * Hands-on experience with Lean and Six Sigma ...

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How much do full time asq cqa jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for full time asq cqa in the United States is $25.32, according to ZipRecruiter salary data. Most workers in this role earn between $20.43 and $28.37 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a full time ASQ Certified Quality Auditor (CQA)?

To thrive as a Full-Time ASQ Certified Quality Auditor, you need a solid understanding of quality management systems, auditing principles, and industry regulations, typically supported by an ASQ CQA certification. Familiarity with auditing tools, statistical analysis software, and documentation systems is crucial for effectively evaluating processes. Strong attention to detail, analytical thinking, and excellent communication skills help auditors identify issues and communicate findings clearly. These skills ensure that organizations maintain compliance, drive continuous improvement, and uphold high-quality standards.

What is a full time ASQ Certified Quality Auditor (CQA)?

A Full Time ASQ CQA refers to a professional who works full-time as a Certified Quality Auditor (CQA), a credential offered by the American Society for Quality (ASQ). These individuals are responsible for auditing, analyzing, and improving organizational quality systems and processes to ensure compliance with industry standards and regulatory requirements. Full Time ASQ CQAs typically plan and conduct audits, prepare reports, and work closely with teams to implement corrective actions. The certification demonstrates expertise in quality auditing principles, practices, and techniques, making these professionals valuable in industries like manufacturing, healthcare, and services.

What is the difference between Full Time Asq Cqa vs Quality Assurance Technician?

AspectFull Time Asq CqaQuality Assurance Technician
CertificationsASQ CQA certification, relevant quality standardsMay have certifications like ASQ CQPA or none
Work EnvironmentManufacturing, aerospace, automotive, regulated industriesManufacturing, food, pharmaceuticals, general industry
ResponsibilitiesQuality system audits, process improvement, complianceProduct inspections, testing, documentation

Full Time ASQ CQA professionals typically hold certifications and focus on quality system audits and compliance in regulated industries. Quality Assurance Technicians often perform product testing and inspections with less emphasis on certification. The CQA role is more strategic and compliance-oriented, while technicians focus on day-to-day quality checks.

What are some common challenges faced by full time ASQ Certified Quality Auditors (CQA), and how can they effectively overcome them?

Full-time ASQ Certified Quality Auditors often encounter challenges such as resistance to audits from colleagues, staying current with evolving standards, and managing multiple audits simultaneously. To overcome these challenges, effective communication skills are essential for building trust and cooperation with auditees. Regular professional development, such as attending workshops and reviewing updated industry guidelines, helps auditors remain knowledgeable. Additionally, strong organizational and time-management skills enable auditors to balance competing priorities and deliver thorough, timely audit reports.
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Full Time Asq Cqa jobs near you
Infographic showing various Full Time Asq Cqa job openings in the United States as of August 2026, with employment types broken down into 94% Full Time, 2% Part Time, and 4% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $52,656 per year, or $25.3 per hour.

Associate Director, Quality Systems Monitoring & Excellence

Revolution Medicines

Redwood City, CA • On-site

Full-time

Posted 3 days ago

New

Job description

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.
The Opportunity:
  • Lead the Global Quality Systems Monitoring & Excellence program to ensure effective governance, compliance, and continuous improvement across the Quality Management System (QMS).
  • Drive global audit and regulatory inspection readiness by leading inspection planning, mock inspections, execution support, response coordination, and post-inspection remediation.
  • Develop and monitor Quality KPIs/KQIs, analyze trends, identify systemic risks, and provide executive reporting through Quality Management Reviews (QMRs).
  • Perform Quality System health assessments and effectiveness reviews to identify compliance gaps and drive sustainable improvements.
  • Oversee CAPA governance related to internal audits & inspections, root cause analysis, effectiveness verification, and closure of audit and inspection commitments.
  • Lead the management of critical quality issues and escalations, facilitate timely cross-functional investigations and remediation plans, and ensure effective resolution of compliance risks and regulatory commitments.
  • Partner with cross-functional stakeholders to standardize, simplify, and optimize Quality processes while ensuring compliance with global GxP regulations.
  • Lead regulatory intelligence activities and translate evolving global regulatory expectations into Quality System enhancements.
  • Leverage AI, automation, data analytics, and digital Quality platforms to enhance compliance monitoring, executive reporting, and operational excellence.
  • Build and lead a high-performing team while fostering a culture of quality, compliance, inspection readiness, and continuous improvement across the organization.

Required Skills, Experience and Education:
  • Bachelor's degree in Life Sciences, Pharmacy, Engineering, Chemistry, or a related scientific discipline; Master's degree preferred.
  • 10+ years of progressive Quality Assurance/Quality Systems experience in the biotechnology, pharmaceutical, or medical device industry, including people leadership.
  • Strong knowledge of global GxP regulations, including FDA, EMA, ICH, and applicable international quality standards.
  • Demonstrated experience leading regulatory inspections, internal audits, Quality Management Reviews (QMRs), and Quality Systems governance.
  • Experience with electronic Quality Management Systems (eQMS), such as Veeva Vault or equivalent.
  • Excellent leadership, communication, strategic thinking, project management, and stakeholder management skills.

Preferred Skills:
  • Experience supporting late-stage clinical development and commercial products.
  • Knowledge of AI-enabled quality solutions, digital transformation, data analytics, and executive dashboard development.
  • Professional certification such as ASQ Certified Quality Auditor (CQA), Certified Manager of Quality/Organizational Excellence (CMQ/OE), RAC, or equivalent is preferred.
  • Demonstrated ability to lead global, cross-functional initiatives and build high-performing teams in a fast-paced, regulated environment.

#LI-JC1 #LI-Hybrid
The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.
Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.
Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.
Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact privacy@revmed.com.
Base Pay Salary Range
$186,000-$233,000 USD
We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message.
Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process. All legitimate communication from Revolution Medicines will come from an official @revmed.com email address.
If you believe you've been contacted by someone impersonating a Revolution Medicines recruiter, please report it to careers@revmed.com so we can share these impersonations with our IT team for tracking and awareness.

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