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Ppap Jobs in California (NOW HIRING)

Expleo

DRE Mcatronique

Los Angeles, CA

Gérer les modifications produit/process et assurer leur validation complète conformément aux standards APQP/PPAP et SOP. * Réaliser et conduire des analyses techniques pour résoudre les ...

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Expleo

DRE Mecatronique

Los Angeles, CA

Gerer les modifications produit/process et assurer leur validation complete conformement aux standards APQP/PPAP et SOP. * Realiser et conduire des analyses techniques pour resoudre les ...

Expleo

DRE Mecatronique vie serie

Los Angeles, CA · On-site

$40K - $55K/yr

Gerer les modifications produit/process et assurer leur validation complete conformement aux standards APQP/PPAP et SOP. * Realiser et conduire des analyses techniques pour resoudre les ...

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All JobsPpap JobsPpap Jobs in California

Ppap information

See California salary details

$24.2K

$56.5K

$85.9K

How much do ppap jobs pay per year?

As of Aug 9, 2026, the average yearly pay for ppap in California is $56,453.00, according to ZipRecruiter salary data. Most workers in this role earn between $43,900.00 and $68,100.00 per year, depending on experience, location, and employer.

What skills and qualifications are needed to thrive as a PPAP coordinator?

To thrive as a PPAP Coordinator, you need a solid understanding of manufacturing processes, quality control, and automotive industry standards, typically supported by experience in quality assurance or engineering. Familiarity with PPAP documentation, statistical process control (SPC) software, and quality management systems like IATF 16949 is important. Strong attention to detail, organizational skills, and effective communication are essential soft skills in this role. These capabilities ensure accurate documentation, compliance with customer requirements, and smooth product launches in highly regulated environments.

What are common challenges faced when managing PPAP documentation in a manufacturing environment?

Managing PPAP (Production Part Approval Process) documentation can be challenging due to the need for precise coordination between suppliers, engineering, and quality teams. Ensuring all required documents are accurate, up-to-date, and submitted on time often requires strong organizational skills and attention to detail. Additionally, frequent changes in customer requirements and engineering revisions can necessitate rapid updates to documentation, making adaptability essential. Effective communication and collaboration with cross-functional teams help overcome these challenges and ensure successful part approvals.

What is the difference between Ppap vs Ppso?

AspectPpapPpso
Required CertificationsTypically requires specific licensing or certification depending on industry standardsOften requires similar certifications, especially in healthcare or social services
Work EnvironmentUsually in clinical, healthcare, or social service settingsSimilar environments, often in healthcare, social work, or community services
Employer & Industry UsageCommonly used in healthcare, social services, and community programsUsed interchangeably in some sectors, especially in healthcare and social work
Common Search & ComparisonOften compared for roles involving patient or client assessmentsCompared for similar responsibilities in service delivery roles

Both Ppap and Ppso roles are integral in healthcare and social services, sharing similar certifications and work environments. The main difference lies in their specific responsibilities and industry terminology, with Ppap often focusing on assessment and planning, while Ppso emphasizes service coordination and support.

What is a PPAP?

PPAP professionals are individuals who specialize in managing and executing the Production Part Approval Process, a standardized process in the automotive and manufacturing industries. They ensure that suppliers meet all customer engineering design and specification requirements before mass production begins. Their responsibilities include submitting documentation, coordinating sample production, and verifying that parts consistently meet quality standards. PPAP professionals play a crucial role in maintaining product quality and fostering strong supplier-customer relationships.
What are popular job titles related to Ppap jobs in California? For Ppap jobs in California, the most frequently searched job titles are:
What job categories do people searching Ppap jobs in California look for? The top searched job categories for Ppap jobs in California are:
Ppap jobs near you
Infographic showing various Ppap job openings in California as of August 2026, with employment types broken down into 83% Full Time, 11% Part Time, 2% Temporary, 3% Contract, and 1% Nights. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $56,453 per year, or $27.1 per hour.

Supplier Quality Engineer / QMS Auditor

Attalon, Inc.

Tustin, CA • On-site

$84K - $144K/yr

Full-time

Re-posted 9 days ago

Job description

Attalon is a U.S.-based aerospace and defense technology company formed through the 2025 carve-out of Coherent's Aerospace & Defense division by Advent International. Attalon designs and manufactures mission-critical optical systems, precision coatings, and advanced laser subsystems for ISR&T, space, missiles, and directed energy applications.

At our Tustin location, we design and manufacture telescopes for applications ranging from targeting pods to deep‑space astronomy, delivering precision optical performance across air, space, and ground platforms.

Supplier Quality Engineer / QMS Auditor

We are seeking a Supplier Quality Engineer / QMS Auditor to join our team and lead efforts in supplier quality management, Quality Management System (QMS) auditing, and PPAP (Production Part Approval Process) coordination. This role is critical to ensuring that our suppliers adhere to established quality standards, industry requirements, and best practices, while also conducting QMS audits to maintain compliance with relevant certifications (e.g., ISO 9001, AS9100). The ideal candidate will bring strong knowledge of quality methodologies, auditing, supplier development, and the ability to drive continuous improvement across the supply chain.

Core Responsibilities:

  • PPAP process management: Ensure supplier compliance during production ramp-up.
  • QMS auditing: Enforce supplier and internal adherence to quality management standards.
  • Supplier accountability: Drive corrective actions and continuous improvement initiatives.
  • Collaboration and reporting: Act as a liaison between suppliers, production teams, and the Quality department.

Supplier Quality Management:

  • Establish, manage, and maintain relationships with suppliers to develop and ensure adherence to quality standards and company policies.
  • Lead and manage PPAP submissions to ensure proper validation of supplier manufacturing processes and components prior to production launch.
    • Review and approve supplier PPAP packages, including dimensional reports, material certifications, control plans, FMEA, and capability studies.
    • Collaborate with suppliers to resolve any discrepancies or issues discovered during the PPAP process.
  • Ensure suppliers' compliance with contract requirements, engineering specifications, and industry standards (e.g., ISO 9001, AS9100, NADCAP).
  • Monitor and evaluate supplier performance using key metrics such as quality defects, delivery performance, and responsiveness to corrective actions.
  • Drive supplier development programs to enhance quality, mitigate risks, and improve manufacturing and operational capabilities.

QMS Auditing and Compliance:

  • Conduct internal audits and supplier audits to ensure compliance with QMS standards (e.g., ISO 9001, AS9100).
  • Evaluate suppliers' Quality Management Systems (QMS) to verify alignment with safety, operational, regulatory, and industry-specific requirements.
  • Manage audit schedules, develop and maintain audit checklists, and prepare audit reports detailing findings, observations, and corrective actions required.
  • Collaborate with suppliers to implement corrective actions and drive continuous improvement based on audit results.
  • Support external third-party QMS audits and ensure proper documentation, record-keeping, and preparation.

Document Control and Regulatory Compliance:

  • Maintain quality documentation, including PPAP records, corrective action plans (CAPA), audit reports, and calibration logs.
  • Ensure document control compliance as part of QMS processes, including revision control, proper storage, and accessibility.
  • Assist suppliers in achieving compliance with relevant regulatory frameworks, such as REACH, RoHS, and Conflict Minerals standards.

Minimum Qualifications

  • Bachelor’s degree in mechanical engineering, Industrial Engineering, Quality Assurance, or related technical field (or equivalent experience).
  • Experience: Minimum 5 years in Supplier Quality Engineering, PPAP coordination, internal auditing, and/or similar quality assurance roles.
  • Direct experience with QMS standards such as ISO 9001, AS9100.
  • Demonstrated knowledge of PPAP processes, including FMEA, process validation methods, and control plans.
  • Proficient in Microsoft Office Suite (Excel, Word, PowerPoint).
  • Experience with quality management software, ERP systems (e.g., SAP, Oracle), and document control platforms.
  • Understanding of engineering drawings, specifications, and GD&T (Geometric Dimensioning and Tolerancing).

Preferred Qualifications

  • Professional certifications such as Certified Quality Auditor (CQA), Certified Quality Engineer (CQE) or Six Sigma Green/Black Belt.
  • Auditor certification for ISO 9001, AS9100, or other relevant standards.
  • Familiarity with Lean Manufacturing and Six Sigma principles.
  • Experience in supplier development and performance metrics reporting.
  • Strong expertise in PPAP processes, quality tools, and statistical techniques (e.g., SPC, Gage R&R, and process capability).
  • Familiarity with regulatory frameworks such as REACH, RoHS, Conflict Minerals, or other industry-specific requirements.
  • Excellent problem-solving abilities utilizing methodologies like 8D, Root Cause Analysis (RCA), and CAPA.
  • Proficient in QMS auditing principles and techniques.
  • Strong written and verbal communication skills for interacting with suppliers and cross-functional teams.
  • Highly organized with strong attention to detail.


For California, the salary pay range for this role is $84,294 - $144,072 per year
Please note this range is provided as a general guideline. When determining an offer, Attalon takes into account multiple factors, including (but not limited to) the responsibilities of the position, your professional experience, education and training, specialized skills, and current market and business conditions.

Equal Opportunity Employer Statement

Attalon, Inc. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.

Export Control Compliance

This role involves access to technology, materials, software, or hardware subject to U.S. export control laws. Therefore, to be considered, candidates must be classified as a “U.S. Person” under applicable regulations or be eligible for authorization under a U.S. government export license.