Quality Manager

Quality Manager

If you would love to be part of a company that is poised for substantial growth with opportunities for career advancement, then working for CPP may be the right fit for you! Join a results-oriented workplace that strives for success through innovation, collaboration, and teamwork.

Consolidated Precision Products (CPP) Euclid is an investment casting foundry that specializes in complex aerospace & gas turbine components. With a stable business model and competitive compensation & benefits, CPP is a great option to consider as you look to make your next career move.

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WHAT WE OFFER

• Weekly Pay for Hourly Employees
• Comprehensive Benefit Plans
• Quarterly Bonus Opportunity
• 401k with Company Match
• Emphasis on Employee Engagement
• Paid Holidays and Vacation Time
• Tuition Reimbursement
• Opportunities for Advancement

JOB SUMMARY

Monitor the quality assurance program which ensures that all products shipped from the facility meets engineering specifications and customer expectations. Drive risk abatement activities and highlight opportunities for improvement.

PRIMARY RESPONSIBILITIES

• Coordinate and assist in writing and updating all procedures and work instructions for each job function in the facility.
• Ensure continuous AS9100 registration, manage internal audit program.
• Monitor product in-process inspections by all manufacturing employees in order to avoid costly final inspection.
• Requisition and monitor all measuring equipment through the manufacturing area.
• Distribute and control revisions to all procedures and work instructions.
• Assist in the investigation and response to all manufacturing related customer complaints.
• Assist engineering in investigating and responding to product performance customer complaints.
• Maintain a quarterly quality report out
• Train employees in the understanding and use of the quality assurance program.
• Train and monitor vendors to ensure they produce product which meets our quality assurance program.
• Disposition the product in the manufacturing area which is found non-conforming to specification.
• Interpret and implement customer specifications for product and quality systems.
• Investigate and recommend corrective actions for engineering related problems in the manufacturing area.
• Assist engineering in design for manufacturing issues.
• Assist in the design and implementation of fixturing for new and existing product.
• Special projects as needed.
• Review and update A3s.
• Corrective Action Reports and follow through.
• Conduct routine and non-routine analyses of in-process materials, raw materials, environmental samples, finished goods, or stability samples.
• Calibrate, validate, or maintain laboratory equipment.
• Compile laboratory test data and perform appropriate analyses.
• Complete documentation needed to support testing procedures including data capture forms, equipment logbooks, or inventory forms.
• Evaluate analytical methods and procedures to determine how they might be improved.
• Identify quality problems and recommend solutions.
• Interpret test results, compare them to established specifications and control limits, and make recommendations on appropriateness of data for release.
• Investigate or report questionable test results.
• Monitor testing procedures to ensure that all tests are performed according to established item specifications, standard test methods, or protocols.
• Participate in out-of-specification and failure investigations and recommend corrective actions.
• Ability to travel to visit customers and vendors as needed.

QUALIFICATIONS

• Education: Bachelors degree and 3-5yrs of manufacturing quality experience. Associates degree and 5-10yrs of manufacturing quality experience. Other combinations of education and experience considered on a case-by-case basis.
• Certifications/Licenses: Certified CQE, SSGB or SSBB is a plus but not required.
• Other Required Knowledge, Skills & Abilities:
  • A comprehensive knowledge of management and quality systems
  • Ability to read, understand and comprehend documents such as safety rules, customer POs, prints and specifications, operating and heat treat schedules, and procedure manuals. Ability to write routine reports and inventory records. Ability to speak effectively before groups of customers or employees in the organization.
  • This person must be a self-starter, able to see what needs to be done, and be creative in the formulation and implementation of plans.
  • The ability to focus on the issues, with unhappy or dissatisfied customers is essential. This individual must be capable of getting to the root of a problem, and not let their emotions interfere with their ability to understand the issues.
  • Knowledge of common statistical analysis and problem-solving quality techniques.

WORKING ENVIRONMENT

• Working Environment: Office Environment
• Physical Demands: Sitting/Standing for extended periods of time, able to lift up to 20lbs, extended periods of time using a computer screen.
• Travel Requirements: 25%
• Safety Glasses: Needed in all areas of the plant.
• Steel toe shoes : Needed in all areas of the plant.
  

NOTE: Consolidated Precision Products is an Equal Employment Opportunity Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, pregnancy, age, disability, veteran status, genetic information, or any other characteristic protected under applicable law. It is the policy of the company to comply with all aspects of the Americans with Disabilities Act. Upon request, the company will provide reasonable accommodations to individuals with disabilities who need an accommodation to fully participate in the application process. All roles are restricted to U.S. persons (U.S. citizens, permanent residents and other protected individuals under the Immigration and Naturalization Act) due to access to export-controlled technology. CPP will require proof of status prior to employment.
Note that we maintain a drug-free workplace, and all offers of employment will be contingent on satisfactory results of a drug & background screen.

This is a full time position