Quality Coordinator/Auditor - Howmet Aerospace

Howmet Aerospace Inc. (NYSE: HWM), headquartered in Pittsburgh, Pennsylvania, is a leading global provider of advanced engineered solutions for the aerospace and transportation industries. Our primary businesses focus on jet engine components, aerospace fastening systems, titanium structural parts and forged wheels. With $6.6 billion in revenue in 2023, our products play a crucial role in enabling fuel efficiency and lightweighting, contributing to our customers' success and making a positive impact on the world. To learn more about the way Howmet Aerospace Inc. is advancing the sustainability of our customers, markets, and communities where we operate, review the 2023 Environmental Social and Governance report at www.howmet.com/esg-report .

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Howmet is proud to be an Equal Employment Opportunity and Affirmative Action employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other applicable legally protected characteristics.

If you need assistance to complete your application due to a disability, please email TalentAcquisitionCoE_Howmet@howmet.comBasic Requirements:

• Bachelor's degree from an accredited college or university in Business, Engineering, or related field
• Minimum of 3 years' experience with preventive Quality Systems
• Employees must be legally authorized to work in the United States. Verification of employment eligibility will be required at the time of hire. Visa sponsorship is not available for this position.

• Minimum of 5 years' experience with preventive Quality Systems Management
• Experience with ASQ Certifications: CQE, CQM, CRE or CSSBB
• Knowledge of Aerospace product/process specification requirements (AMS, ASTM, etc.)
• Experience in product and process failure analysis and an understanding of quality principles (SPC, TQM,

• Bachelor's degree from an accredited college or university in Business, Engineering, or related field
• Minimum of 3 years' experience with preventive Quality Systems
• Employees must be legally authorized to work in the United States. Verification of employment eligibility will be required at the time of hire. Visa sponsorship is not available for this position.

• Minimum of 5 years' experience with preventive Quality Systems Management
• Experience with ASQ Certifications: CQE, CQM, CRE or CSSBB
• Knowledge of Aerospace product/process specification requirements (AMS, ASTM, etc.)
• Experience in product and process failure analysis and an understanding of quality principles (SPC, TQM,

We're currently seeking highly motivated and energetic people to join our team as an Quality Assurance Coordinator II at our Howmet Fastening Systems (HFS) manufacturing facility in Carson, CA.; a business unit within Howmet Aerospace, a leading global provider of advanced engineered solutions for the aerospace and transportation industries. The Company's primary businesses focus on jet engine components, aerospace fastening systems and titanium structural parts necessary for mission-critical performance and efficiency in aerospace and defense applications, as well as forged wheels for commercial transportation. Howmet Aerospace is transforming the next phase of more fuel-efficient, quieter aerospace engines and sustainable ground transportation. For more information, visit www.howmet.com. Follow @howmet: Twitter, Instagram, Facebook, LinkedIn and YouTube.

Under the direction of the Quality Manager, is managing external QMS audits, the Internal Audit system, Documentation Control & Corrective Actions systems supporting compliance to the QMS, Customer and AS9100 requirements.

Key Responsibilities:

• Manage Internal Audit system:
  • Develop internal audit schedules, assign auditors, monitor system performance & provide routine updates to Factory Managers.
  • Coordinate with Factory Managers to identify & train internal auditors within the facility to ensure adequate resources are maintained to guarantee compliance.
  • Manage external QMS audits and Customer systems surveys. Assist area managers as needed to maintain compliance to their documented processes.
• Manage Document Control system:
  • Review and release of documents in the document control data base. Work with Factory Managers to ensure a timely release of document updates. Provide routine updates of Document Control system performance to Factory Management.
  • Update and augment group Quality Assurance procedures and systems based on QMS/AS9100 updates and/or audit findings.
  • Manage and coordinate the archiving and retrieval of critical build records with outsourced supplier.
• Manage Corrective Action system:
  • Routinely monitor Corrective Action system to ensure timely response on all open Corrective Actions.
  • Screen all Corrective Action responses for effective root cause determination & mitigation reaction prior to submitting for management review.
  • Monitor CA system performance & provide routine updates/trends to Factory Management.
• Additional responsibilities include, but are not limited to:
  • Preparing, processing & tracking RFA requests and requisition submittals.
  • Preparing monthly Corrective Action Board meetings and yearly Management Reviews.
  • Preparing and updating the 360 Boards with key performance indicator charts
  • Providing support as deemed necessary by management to allow the Quality Department to function efficiently.
  • Perform other duties as may be assigned by the Quality Manager.

The position includes competitive wages and a comprehensive benefits package, including health insurance (medical, dental, vision), excellent 401k matching program, paid holidays, and vacation. The salary range for this position is $68K to $75K.Quality Assurance Coordinator

We're currently seeking highly motivated and energetic people to join our team as an Quality Assurance Coordinator II at our Howmet Fastening Systems (HFS) manufacturing facility in Carson, CA.; a business unit within Howmet Aerospace, a leading global provider of advanced engineered solutions for the aerospace and transportation industries. The Company's primary businesses focus on jet engine components, aerospace fastening systems and titanium structural parts necessary for mission-critical performance and efficiency in aerospace and defense applications, as well as forged wheels for commercial transportation. Howmet Aerospace is transforming the next phase of more fuel-efficient, quieter aerospace engines and sustainable ground transportation. For more information, visit www.howmet.com. Follow @howmet: Twitter, Instagram, Facebook, LinkedIn and YouTube.

Under the direction of the Quality Manager, is managing external QMS audits, the Internal Audit system, Documentation Control & Corrective Actions systems supporting compliance to the QMS, Customer and AS9100 requirements.

Key Responsibilities:

• Manage Internal Audit system:
  • Develop internal audit schedules, assign auditors, monitor system performance & provide routine updates to Factory Managers.
  • Coordinate with Factory Managers to identify & train internal auditors within the facility to ensure adequate resources are maintained to guarantee compliance.
  • Manage external QMS audits and Customer systems surveys. Assist area managers as needed to maintain compliance to their documented processes.
• Manage Document Control system:
  • Review and release of documents in the document control data base. Work with Factory Managers to ensure a timely release of document updates. Provide routine updates of Document Control system performance to Factory Management.
  • Update and augment group Quality Assurance procedures and systems based on QMS/AS9100 updates and/or audit findings.
  • Manage and coordinate the archiving and retrieval of critical build records with outsourced supplier.
• Manage Corrective Action system:
  • Routinely monitor Corrective Action system to ensure timely response on all open Corrective Actions.
  • Screen all Corrective Action responses for effective root cause determination & mitigation reaction prior to submitting for management review.
  • Monitor CA system performance & provide routine updates/trends to Factory Management.
• Additional responsibilities include, but are not limited to:
  • Preparing, processing & tracking RFA requests and requisition submittals.
  • Preparing monthly Corrective Action Board meetings and yearly Management Reviews.
  • Preparing and updating the 360 Boards with key performance indicator charts
  • Providing support as deemed necessary by management to allow the Quality Department to function efficiently.
  • Perform other duties as may be assigned by the Quality Manager.

The position includes competitive wages and a comprehensive benefits package, including health insurance (medical, dental, vision), excellent 401k matching program, paid holidays, and vacation. The salary range for this position is $68K to $75K.