Deep expertise in IATF 16949, ISO 9001, APQP, PFMEA/DFMEA, Control Plans, CAPA, and risk management. * Ability to read, write, speak, and understand English sufficiently to perform the essential ...
Deep expertise in IATF 16949, ISO 9001, APQP, PFMEA/DFMEA, Control Plans, CAPA, and risk management. * Ability to read, write, speak, and understand English sufficiently to perform the essential ...
Quality Supervisor
Phoenix, AZ · On-site
... management. Candidates should maintain current knowledge of industry testing practices and ... Lead corrective and preventive action (CAPA) activities by identifying root causes, implementing ...
Quick apply
Quality Supervisor
Phoenix, AZ · On-site
... management. Candidates should maintain current knowledge of industry testing practices and ... Lead corrective and preventive action (CAPA) activities by identifying root causes, implementing ...
Quality Supervisor
Phoenix, AZ · On-site
... management. Candidates should maintain current knowledge of industry testing practices and ... Lead corrective and preventive action (CAPA) activities by identifying root causes, implementing ...
Quality Supervisor
Phoenix, AZ · On-site
... management. Candidates should maintain current knowledge of industry testing practices and ... Lead corrective and preventive action (CAPA) activities by identifying root causes, implementing ...
Quality Supervisor
Phoenix, AZ · On-site
... management. Candidates should maintain current knowledge of industry testing practices and ... Lead corrective and preventive action (CAPA) activities by identifying root causes, implementing ...
Quality Supervisor
Phoenix, AZ · On-site
... management. Candidates should maintain current knowledge of industry testing practices and ... Lead corrective and preventive action (CAPA) activities by identifying root causes, implementing ...
Senior Quality & Manufacturing Lead
Chandler, AZ · On-site +1
Experience with manufacturing audits, supplier management, and production process validation. * Knowledge of quality methodologies including CAPA, FMEA, SPC, 8D, and root cause analysis tools.
Senior Quality & Manufacturing Lead
Chandler, AZ · On-site +1
Experience with manufacturing audits, supplier management, and production process validation. * Knowledge of quality methodologies including CAPA, FMEA, SPC, 8D, and root cause analysis tools.
Validation Engineer and CQV
Chandler, AZ · On-site
$45K - $50K/yr
Knowledge of change controls, deviations, CAPA, and quality management systems. * Experience working in FDA-regulated pharmaceutical or sterile manufacturing facilities. * Familiarity with ...
Validation Engineer and CQV
Chandler, AZ · On-site
$45K - $50K/yr
Knowledge of change controls, deviations, CAPA, and quality management systems. * Experience working in FDA-regulated pharmaceutical or sterile manufacturing facilities. * Familiarity with ...
Quality Director
Tempe, AZ · On-site
The Quality Director provides strategic leadership and oversight across Quality Assurance and Quality Control, including deviation management, CAPA, change control, document control, training ...
Quality Director
Tempe, AZ · On-site
The Quality Director provides strategic leadership and oversight across Quality Assurance and Quality Control, including deviation management, CAPA, change control, document control, training ...
GTM Strategy & Integration Specialist
Phoenix, AZ · On-site
$55 - $65/hr
... manage the enterprise marketing calendar, and coordinate cross-functional teams from planning through launch and post-campaign communication. You'll also serve as a steward of CEA CAPA's content ...
New
GTM Strategy & Integration Specialist
Phoenix, AZ · On-site
$55 - $65/hr
... manage the enterprise marketing calendar, and coordinate cross-functional teams from planning through launch and post-campaign communication. You'll also serve as a steward of CEA CAPA's content ...
New
QA Investigations Specialist
Gilbert, AZ · On-site
$85 - $120/hr
Ensure CAPA actions are practical, risk-based, and aligned with regulatory and company standards ... Contribute to enhancement of site procedures for deviation and OOS management. Qualifications
New
QA Investigations Specialist
Gilbert, AZ · On-site
$85 - $120/hr
Ensure CAPA actions are practical, risk-based, and aligned with regulatory and company standards ... Contribute to enhancement of site procedures for deviation and OOS management. Qualifications
New
Clinical Research Site Director - Phoenix, Arizona
Phoenix, AZ · On-site
$90 - $130/hr
Lead and manage clinical research staff and operations. * Develop and implement SOPs to ensure GCP ... Monitor quality metrics, audits, and CAPA plans. * Direct all site operations. Requirements * 5+ ...
Clinical Research Site Director - Phoenix, Arizona
Phoenix, AZ · On-site
$90 - $130/hr
Lead and manage clinical research staff and operations. * Develop and implement SOPs to ensure GCP ... Monitor quality metrics, audits, and CAPA plans. * Direct all site operations. Requirements * 5+ ...
Director, Quality Programs (PMO)-Ambulatory Monitoring & Diagnostics
Phoenix, AZ · On-site
$162 - $258/hr
... CAPA processes, Nonconformance, Process Controls, etc. * You're highly experienced in all aspects of E2E global Program Management including 5+ years in strategic/cross-functional leadership, change ...
Director, Quality Programs (PMO)-Ambulatory Monitoring & Diagnostics
Phoenix, AZ · On-site
$162 - $258/hr
... CAPA processes, Nonconformance, Process Controls, etc. * You're highly experienced in all aspects of E2E global Program Management including 5+ years in strategic/cross-functional leadership, change ...
... CAPA processes, Nonconformance, Process Controls, etc. * You're highly experienced in all aspects of E2E global Program Management including 5+ years in strategic/cross-functional leadership, change ...
... CAPA processes, Nonconformance, Process Controls, etc. * You're highly experienced in all aspects of E2E global Program Management including 5+ years in strategic/cross-functional leadership, change ...
Quality Manager for PCBA Electronic Assembly
Phoenix, AZ · On-site
$90K - $130K/yr
Maintain and participate in the audit of robust Quality Management System (QMS) frameworks to address and mitigate non-conformances, enforcing root-cause and corrective actions (CAPA/RCCA)
Quick apply
Quality Manager for PCBA Electronic Assembly
Phoenix, AZ · On-site
$90K - $130K/yr
Maintain and participate in the audit of robust Quality Management System (QMS) frameworks to address and mitigate non-conformances, enforcing root-cause and corrective actions (CAPA/RCCA)
Quality Manager for PCBA Electronic Assembly
Phoenix, AZ · On-site
$90K - $130K/yr
Maintain and participate in the audit of robust Quality Management System (QMS) frameworks to address and mitigate non-conformances, enforcing root-cause and corrective actions (CAPA/RCCA)
Quality Manager for PCBA Electronic Assembly
Phoenix, AZ · On-site
$90K - $130K/yr
Maintain and participate in the audit of robust Quality Management System (QMS) frameworks to address and mitigate non-conformances, enforcing root-cause and corrective actions (CAPA/RCCA)
Quality Manager for PCBA Electronic Assembly
Phoenix, AZ · On-site
$90K - $130K/yr
Maintain and participate in the audit of robust Quality Management System (QMS) frameworks to address and mitigate non-conformances, enforcing root-cause and corrective actions (CAPA/RCCA)
Quality Manager for PCBA Electronic Assembly
Phoenix, AZ · On-site
$90K - $130K/yr
Maintain and participate in the audit of robust Quality Management System (QMS) frameworks to address and mitigate non-conformances, enforcing root-cause and corrective actions (CAPA/RCCA)
Manufacturing Quality Engineer II (Onsite)
$72K - $93K/yr
... CAPA), validation plans, CTQ identification, FAIR/PPAP documentation, and quality monitoring implementation. * Lead nonconforming material review (NCMR/MRB) and manage material dispositions with ...
Manufacturing Quality Engineer II (Onsite)
$72K - $93K/yr
... CAPA), validation plans, CTQ identification, FAIR/PPAP documentation, and quality monitoring implementation. * Lead nonconforming material review (NCMR/MRB) and manage material dispositions with ...
Staff Engineer Quality Process
Chandler, AZ · On-site
$89 - $149/hr
Risk Management, CAPA, Audits, Statistics). * Must possess strong communication, project management and influencing skills as well as have the ability to manage multiple tasks simultaneously.
Posted today
Staff Engineer Quality Process
Chandler, AZ · On-site
$89 - $149/hr
Risk Management, CAPA, Audits, Statistics). * Must possess strong communication, project management and influencing skills as well as have the ability to manage multiple tasks simultaneously.
Posted today
Quality & Safety Lead
Phoenix, AZ · Remote
$95K - $105K/yr
The position leads audit programs, corrective and preventive action (CAPA) processes, and performance management systems across both disciplines. Acting as a force multiplier for operations ...
Quick apply
Quality & Safety Lead
Phoenix, AZ · Remote
$95K - $105K/yr
The position leads audit programs, corrective and preventive action (CAPA) processes, and performance management systems across both disciplines. Acting as a force multiplier for operations ...
Deep expertise in IATF 16949, ISO 9001, APQP, PFMEA/DFMEA, Control Plans, CAPA, and risk management. * Ability to read, write, speak, and understand English sufficiently to perform the essential ...
Deep expertise in IATF 16949, ISO 9001, APQP, PFMEA/DFMEA, Control Plans, CAPA, and risk management. * Ability to read, write, speak, and understand English sufficiently to perform the essential ...
Quality Engineer CTSE
Gilbert, AZ · On-site
$95 - $135/hr
Open, investigate, and manage Supplier CAPA through verification and closure. * Support strong cross functional relationships with Engineering, Production, Supply Chain, and Program Management.
Quality Engineer CTSE
Gilbert, AZ · On-site
$95 - $135/hr
Open, investigate, and manage Supplier CAPA through verification and closure. * Support strong cross functional relationships with Engineering, Production, Supply Chain, and Program Management.
Capa Manager information
What does a CAPA manager do?
A CAPA (Corrective and Preventive Action) Manager is responsible for overseeing an organization's CAPA process to ensure compliance with quality and regulatory requirements. They investigate quality issues, identify root causes, and implement corrective and preventive measures to prevent recurrence. CAPA Managers work closely with cross-functional teams to improve processes, maintain regulatory compliance, and enhance overall product or service quality.
What are the key skills and qualifications needed to thrive as a CAPA manager?
To thrive as a CAPA Manager (Corrective and Preventive Action Manager), you typically need a background in quality assurance, strong analytical and problem-solving abilities, and experience with regulatory compliance, often supported by a degree in a science or engineering field. Familiarity with quality management systems (QMS), risk management tools, root cause analysis methodologies (such as 5 Whys or Fishbone diagrams), and industry certifications like Six Sigma or ISO 9001 are highly valued. Outstanding candidates demonstrate excellent communication, leadership, and organizational skills to effectively drive cross-functional teams and ensure timely resolution of quality issues. These skills are crucial for identifying, addressing, and preventing compliance gaps or product issues, thereby maintaining high standards and avoiding costly regulatory penalties.
What are some common challenges a CAPA manager faces, and how are they typically addressed?
One common challenge CAPA Managers face is ensuring timely and thorough investigations into quality issues while coordinating input from multiple departments. Balancing the need for fast resolution with the rigor required for regulatory compliance can be demanding, especially in highly regulated industries like pharmaceuticals or medical devices. Successful CAPA Managers often address these challenges through clear process documentation, effective project management, and fostering strong collaboration among stakeholders. By leveraging root cause analysis tools and maintaining open communication, they help create a continuous improvement culture that benefits both the organization and its customers.
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For Capa Manager jobs in Phoenix, AZ, the most frequently searched job titles are:
What job categories do people searching Capa Manager jobs in Phoenix, AZ look for?
The top searched job categories for Capa Manager jobs in Phoenix, AZ are:
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Cities near Phoenix, AZ with the most Capa Manager job openings:
Full-time
Re-posted 28 days ago
Lucid Motors rating
7.4
Based on 37 frontline employees who took The Breakroom Quiz
17th of 45 rated automakers
Job description
Sr. Manager, Quality Management System (QMS)
Quality | Phoenix, AZ | Full-Time
About Lucid
At Lucid, we are creating an electric future without compromise. That means refusing to choose between performance and sustainability, design and engineering, ambition and integrity. We build world-class vehicles by pushing performance, efficiency, and design beyond industry limits, setting new standards with vehicles like Lucid Air and Lucid Gravity.
The Role
The Senior Manager, Quality Management System (QMS) is responsible for developing, maintaining, and leading Lucid's enterprise-level Quality Management System in alignment with IATF 16949, ISO 9001, internal standards, and applicable regulatory requirements. This role drives cross-functional governance, compliance, continuous improvement, and systemic quality excellence across Manufacturing, Engineering, Supply Chain, Field Quality, and Customer Experience.
What You'll Own
- Quality Management System Leadership
- Audit & Compliance Oversight
- Process Governance & Standardization
- Change Management & Continuous Improvement
- Training & Organizational Development
- Leadership & People Management
What You Bring
Required
- Bachelor's degree in Engineering, Quality, Manufacturing, Industrial Engineering, or a related technical field.
- 12+ years of progressive experience in Quality Management Systems, Quality Engineering, Manufacturing Quality, or Regulatory Compliance.
- 5+ years of leadership experience managing teams and influencing cross-functional stakeholders.
- Hands-on experience leading an IATF 16949 and/or ISO 9001 certified Quality Management System.
- Deep expertise in IATF 16949, ISO 9001, APQP, PFMEA/DFMEA, Control Plans, CAPA, and risk management.
- Ability to read, write, speak, and understand English sufficiently to perform the essential duties of the position, including understanding work instructions, safety procedures, and job-related communications.
Preferred
- Master's degree in Engineering, Quality, Manufacturing, Business Administration, or related discipline.
- ASQ CQE, CMQ/OE, or related certifications.
- Experience leading enterprise QMS transformation or digital quality initiatives.
- Electric vehicle manufacturing experience.
Work Requirement
Regular onsite engagement is required to support governance activities, audits, process reviews, and strategic quality initiatives.
Compensation and Benefits
Base salary range: [Compensation Range TBD]. Lucid offers a comprehensive and competitive benefits package.
Equal Opportunity
At Lucid, we believe diversity strengthens everything we build. Lucid Motors is proud to be an equal opportunity employer and is committed to providing an inclusive workplace for all.
Accessibility
Lucid Motors is committed to providing reasonable accommodations for qualified individuals with disabilities.
Candidate Data Privacy
By submitting your application, you understand and agree that your personal data will be processed in accordance with our Candidate Privacy Notice.
To All Recruitment Agencies
Lucid Motors does not accept agency resumes and is not responsible for fees related to unsolicited resumes.
What Lucid Motors employees say
Pay
Benefits
Hours and flexibility
Workplace
Get the full story on Breakroom
About Lucid Motors
Sourced by ZipRecruiter
Lucid Motors is a highly innovative electric vehicle manufacturer located in Newark, CA, USA. Primarily engaged in the automotive industry, its mission is to elevate electric vehicles' standing and transform the way people travel. The company was founded in 2007 by Bernard Tse and Sam Weng as Atieva, a name under which it initially focused on battery technology. However, it pivoted towards automotive manufacturing and rebranded as Lucid Motors in 2016. The company is committed to making luxury, sustainable electric vehicles that break norms and set new standards with top-notch technology and engineering. Their mission aligns with their core values, which are centered around innovation, sustainability, and excellence. Notably, Lucid Motors launched the Lucid Air in 2020, an all-electric sedan well-received for its advanced features and impressive mileage.
Industry
Manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Newark, CA, US
Year founded
2007