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ASQ Job Opportunities

Posted: July 17, 2010
Quality Engineer
Hagerthy & Company

Quality Engineer

Department Division: Quality Assurance
Exempt or Non-Exempt Position: Exempt
Location: Orange County, CA

Company

Our client manufacturers a line of universal adapters, chargers and accessories that provide power and charging functionality for popular electronic devices and wireless accessories. Their products are designed for the mobile professional who regularly carries several pieces of equipment, all of which can now be charged by a single power system. They have a great technology and are scrambling to meet demand.  If you’re interested in working in a growing company that is fast-paced, and at times, a little chaotic, then this is a good opportunity for you.   

Job Scope and Dimensions

Supports activities related to the development and qualification of new product development to ensure quality is part of the design and development process, as well as supporting existing products. Works with management and technical staff in performing root cause failure analysis, then suggests and implements corrective and preventive actions to preclude recurrence. Provides support in the development and maintenance of the company’s quality systems

Examples of Duties and Responsibilities of the Job

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Perform Failure Analysis and Root Cause Analysis to determine the cause of failure in order to implement corrective actions

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Prepare and present Failure Analysis Report for internal and external use in communicating the findings of failure analysis

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Ensure timely resolution of supplier failure, corrective actions and preventive actions

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Participate in cross-functional teams throughout the development process to ensure quality design of products

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Interface with Engineering and Operations to ensure transfer to Production of new products are in accordance with corporate policy

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Participate in First Article approval process, to include reviewing and approving the reports submitted by suppliers

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Develop statistical data to determine present standards and establish process reliability

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Create and implement final inspection criteria and procedures

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Direct manufacturing personnel engaged in inspection and testing activities to ensure routine process verification reporting

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Work with vendors to insure quality of purchased parts for company use

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Coordinate, perform, and report design verification and validation activities

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Develop design control deliverables including Quality Plans, Manufacturing & Inspection documentation, test methods, and Device History Records

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Ensure all products meet the product specification requirements

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Drive corrective actions through Engineering on all Deviations from the Design Specifications

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Coordinate with engineering department to establish operations for prototypes, First Articles, new releases and other production requirement as needed

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Ensure ISO procedures are being adhered to and coordinate ISO compliance activities

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Drive corrective and preventive action report program

Experience

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Knowledge of ISO Certification (standards & compliance.)

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Knowledge of IPC 610

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Knowledge of SPC

Technical Skills

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Working knowledge of desktop computer office software and e-mail is required

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Working knowledge of SPC and FMEA software is desired

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Able to multi-task

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Thorough knowledge of engineering drawings

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Working knowledge of MTBF qualification

Education / Training

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4 years college degree and/or 7 years or more of relevant experience

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ASQ Certificates preferable

Contact

Mike Hagerthy
Hagerthy & Co.
Executive Search/Training/Consulting
609 Deep Valley Drive, Suite 200
Rolling Hills Estates, CA 90274
(310) 265-4406 Office
mike@hagnco.com
www.hagnco.com

Posted: July 12, 2010
Sr. Quality Engineer
Accellent, Inc.

Accellent, Inc. is a fully integrated provider of design, supply chain management and strategic sourcing services to the Medical Device industry. Accellent www.accellent.com, a recognized market leader, is a fast-growing outsource manufacturing and design solution company specializing in high growth areas such as Cardiology, Endoscopy and Orthopaedics. The top Medical Device companies partner with Accellent to provide innovation, advanced technology, speed to market, low cost labor and strategic sourcing. 

This position will be integral in meeting the Quality Management System requirements.  It requires creativity and foresight to work with operations and product development teams to ensure compliance to the Quality Manual, Design Control, Supplier Management and other appropriate procedures for a variety of medical devices from concept through market introduction.  The ideal candidate is a self-motivated individual who is excited by the prospect of working in a dynamic, fast-paced environment.

We are currently seeking a Sr. Quality Engineer for our Upland, CA site.

Responsibilities:

·         Maintain company compliance with FDA Quality System Regulations and ISO 13485 standards,.  Experience with FDA and ISO inspections and registration is a plus.

·         Actively participates in internal audits, management review and other activities covered under Accellent Quality Manual, Policies and Procedures.

·         Provide customer related quality and regulatory inquiries support.

·         Compiles and writes training material and conducts training sessions on quality control activities.

·         Provide QE direction, analysis and recommendations for product Development to successfully launch new products into active production in a timely and cost effective manner.  Directs development and maintenance of internal/external standards relative to Design and Development.

·         Lead implementation of continuous improvement project or act as subject matter expert for SPC, FMEA, DOE, and process validations

·         Lead and provide Project Management support as needed

·         Develops and initiates standard methods for inspection, testing, and evaluations, utilizing knowledge in related engineering fields.

·         Devises sampling procedures and designs and develops forms and instructions for recording, evaluating, and reporting quality and reliability data.

·         Performs measurement system analysis to evaluate test and inspection equipment

·         Leads disposition of discrepant material and devises process to assess product quality and reliability

·         Monitors and directs engineering group on calibration requirements and implementation of systems to support equipment calibration

·         Lead supplier approval and qualification of new/revised items which includes inspection method development and validation as well as correlation with supplier's methods, supplier audits, management of supplier corrective and preventative actions and assist in FMEA

·         Direct support for FDA and ISO inspections and registration

·         Directs workers engaged in measuring, testing, and tabulating data concerning quality and reliability

·         Up to 10% travel may be required

 Requirements:

 ·         5 -8 years experience in the Medical Device or other regulated industry, such as QSR and ISO 13485, with increasing responsibility.

·         Experience with FDA and ISO 13485 Certification inspections is a plus.

·         3 years Project Management experience, supervising diverse teams

·         Quality Engineering certification (CQE) preferred or equivalent body of knowledge in areas which include, but are not limited to Statistics, SPC, Geometric
    Dimensioning/Tolerancing (GD&T); Sampling, Design of Experiments.

·         Ability to analyze, understand and effectively communicate this technical material.  Experience with Lean Manufacturing and Six sigma is a plus

·         Ability to organize and judge priorities in a dynamic, fast-paced environment and work independently with minimal supervision.

·         Must have excellent verbal & written communication skills, which include but are not limited to presentation, organizational and management skills.

 Please submit your resume to:

 
Accellent is an Equal Opportunity/Affirmative Action employer and we value diversity in our workforce. As such we provide equal opportunity for all applicants without regard to race, religion, gender, national origin, age, marital status, veteran status, or disability. To learn more about Accellent and our career opportunities, please visit us at www.accellent.com 
 

Posted: May 18, 2010
Quality Control Engineer
for an Industry Leading Fortune 500 Global Manufacturing Company

Quality Engineer

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BS Engineering

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Works with quality, sales, engineering, and operations personnel to drive continuous improvement in products and processes.

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Takes a leadership role on continuous improvement teams to drive root cause analyses and corrective action plans.

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Acquires, sorts and analyzes performance data to identify adverse trends and improvement opportunities.

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Participates in product design activities and contract reviews to determine conformance to customer requirements.

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Performs quality and reliability assessments for recommended product improvements.

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Participate and lead Material Review Board (MRB) activity

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Validate Assembly and Test Procedures

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Develop Flow Charts, Process Failure Modes and Effective Analysis (PFMEA) and Control Plans for product families and processes

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Must have strong writing, presentation, planning, problem solving, organizational, project management and decision-making skills.

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Knowledge of Government/Customer contracts experience

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Familiar with the Federal Acquisition Regulations (FAR), Defense Federal Acquisition Regulations (DFAR), and Aerospace Customers’ Requirements

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Demonstrated aptitude for process improvement and use of Lean and Six-Sigma resources and tools during Root Cause Analyses

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Knowledge of aerospace quality standards including AS9100, ISO and FAR 145  

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Working knowledge of CAD (CATIA V5 or Solidworks) would be a plus.  

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Working knowledge of ANSI Y14.5

Anyone interested, please email resume to rybarra@purcellintl.com 

Posted: March 18, 2010
Quality Control Engineer
Wilden Pump & Engineering Company, Grand Terrace CA

Quality Control Engineer

SUMMARY:  

The Quality Engineer will utilize analytical tool and techniques to define, quantify, and improve product and process quality. The candidate will apply engineering / technical skills and statistical techniques to make recommendations and carry out quality improvements.  The focus of this position will be on the continual improvement of existing processes, and supporting the efforts of the development and process validation of new processes. The successful candidate will also apply problem solving techniques to identify and resolve quality issues to ensure customer satisfaction.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

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Lead QA/RA efforts by actively participating as member of cross-functional team (as assigned) and ensuring quality compliance and best practices in areas of design, and manufacturing.

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Lead/Support key QA/RA activities, as assigned. May include, but are not limited to activities in the following areas:

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Design and Development activities

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Production and Process Controls in molding

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QA investigation and root cause analysis of customer returns / complaints.

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NCMR/CAPA, complaints, FMEA, and risk management

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Supplier Quality Management, including Supplier Qualification, Supplier Rating Systems, and development of inspection plans.

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Write validation (IQ, OQ, PQ) protocols, perform or manage performance of protocols, analyze data and write validation reports.

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Support company goals and objectives, policies and procedures, and quality systems.

QUALIFICATIONS REQUIREMENTS:

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Software experience: Minitab Statistical Software, MS Office.

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Experience in statistics, including DOE and gauge repeatability and reproducibility.

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Demonstrated effective interpersonal and networking skills.

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Will be expected to earn Six-Sigma Green Belt certification during first year of employment, if not already certified.

EDUCATION and/or EXPERIENCE:

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Technical degree—BS in quality engineering or equivalent

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Minimum 3 to 5 years experience working in quality control / assurance environment.

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Six-Sigma Green Belt certification preferred

PHYSICAL DEMANDS:

Requirements of this position include the ability to lift 50 pounds

STATEMENT OF NON-INCLUSIVITY

This job description is not to be construed as a complete listing of the duties and responsibilities that may be given to any employee.  The duties and responsibilities outlined in this position may be added to or changed when deemed appropriate and necessary by the person who is managerially responsible for this position.

WE ARE AN EQUAL OPPORTUNITY EMPLOYER.

Please contact:

Silvia Cintron

Human Resources Manager

Wilden Pump & Engineering Company
Phone: (909) 512-1217
Fax:     (909) 512-1249
Email: 
silvia.cintron@wildenpump.com

www.wildenpump.com

Posted: March 5, 2010
Manager - Continuous Improvement
CIRCOR Aerospace Products Group·
Corona, CA

JOB TITLE:  Manager – Continuous Improvement

BUSINESS:  CIRCOR Aerospace Products Group

LOCATION:  Corona, California, USA

SALARY RANGE:  Competitive

ABOUT THE CIRCOR AEROSPACE PRODUCTS GROUP:

The CIRCOR Aerospace Products (CAP) Group is headquartered in Corona, CA and is currently comprised of five businesses that are leaders in the design, development and manufacture of aircraft components and sub-systems, including landing gear, fluid controls and high performance switches.   

These businesses include CIRCOR Aerospace, Inc in Corona, California (former Circle Seal Controls and LOUD Engineering & Manufacturing); Aerodyne Controls in Ronkonkoma, New York; Motor Technologies in Dayton, Ohio, Industria in Paris, France and Bodet Aero of Chemille, France and the related ATLAS Productions, Tangier, Morocco.

The CAP group has annual global sales of over $110 million.  The Aerospace Group is part of CIRCOR International (NYSE:CIR) headquartered in Burlington, Massachusetts.  www.circor.com

CIRCOR Aerospace Products are utilized in nearly all commercial and military aircraft, commercial and military helicopters, space launch vehicles, including the US Space Shuttle, commercial and military ships and submarines, as well as numerous industrial and high technology applications.  www.circoraerospace.com

JOB FUNCTION / PURPOSE:

The CIRCOR Aerospace Product, Inc. – Manager of Continuous Improvement is responsible for the planning, management and execution of factory improvement projects to fulfill the strategic objectives of the continuous improvement program office and business strategy of the aerospace business.

This leader is the primary resource for leading the Aerospace group’s continuous improvement through the planning and implementation of Lean manufacturing and Six Sigma methodologies.   Partners with corporate CI office, group business and operations leadership to ensure the transformation to a culture of operational excellence and continuous improvement.   

Delivers practical, hands-on training to associates on Lean manufacturing methodology and tools to eliminate waste in all administrative, manufacturing and support functions.  Measures and reports progress for group level activities on an on-going basis.  Assures standardization of Lean methodologies and drives keeping lean definitions, tools, certification and benchmarking efforts up to date for the group team of lean practitioners

REPORTING STRUCTURE AND KEY RELATIONSHIPS

The Continuous Improvement Manger interfaces with various internal business partners to ensure the planning, training, execution and measurement of continuous improvement efforts for the Aerospace Business of CIRCOR

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Reports To:  General Manager, CIRCOR Aerospace Inc.

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Direct Reports:  Continuous Improvement Personnel within the business unit.

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Key Internal Partners:  Manufacturing Engineering, Quality Engineering, Operations Leadership, Manufacturing Leadership, Material Planning

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Customers:  CAI Leadership Team

PRINCIPLE ACTIVITIES / RESPONSIBILITIES:

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Ensures the development of a robust Lean Future State Strategy to be implemented across the Aerospace group.  Provides oversight and guidance for all Continuous Improvement initiatives within the organization.  Champions all aspects of the Company’s Operational Excellence Strategy in partnership with business leaders and key operations leadership. 

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Works with Business Units on Lean implementations.   Ensures progression of the Lean Journey and adherence to standards at all levels, while training the CAI staff.   

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Ensures that the organization is structured and has the talent, resources and organizational capability (readiness) for lean transformation; Gives feedback to leadership and HR on talent needs and organizational capability (people & process) needed to achieve higher and higher levels of continuous improvement.   

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Ensures the Site, Value Stream and Team Improvement boards meet standards, enabling a PDCA culture in multi-site business units.  Provides high level of technical and operational recommendations in meeting productivity, material control, product quality, on-time delivery and customer service goals. 

ACCOUNTABILITIES:

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Ensures on-going education of all employees at the Business unit in Lean.  Promotes a Continuous  Learning environment through development and delivery of all intellectual property. 

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Communicates the status of all Lean efforts to the Leadership Team.  Provides documentation of results and benefits achieved. 

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Shares “best practice” methods and ideas with all Continuous Improvement Leaders. 

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Analyzes, interprets and recommends the use of Lean methodologies for improved profitability and continued growth, including product line repositioning and structural changes, as appropriate. 

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Acts as the primary contact for Lean consulting relationship with TBM and other Lean and Six Sigma consultants

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Works with business unit management to establish the budgetary requirements of the Continuous Improvement function and Lean investment. Prepares budgets, performs analysis, and recommends how to maximize return on investments. 

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Defines and manages lean sigma certification program within CAI, including cultural maturity assessments and succession plans.

EDUCATION, EXPERIENCE, AND COMPETENCIES:

Education:  Undergraduate degree in Supply Chain, Engineering or other technology or science related areas preferred.  Certified lean and six sigma required, with demonstrated project success.

Experience:  5-10 years of progressive materials, manufacturing and operations team management experience, with Aerospace and Defense operations experience preferred.  Must have successfully led a minimum of twenty five (25) Kaizen events, typically five-day events, within a manufacturing environment.  Has participated in numerous other Kaizen events preferably in both the manufacturing and office areas. Good understanding of financial measurements and goals in the Lean/Flow throughput world.

Core Competencies:

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High ethical standards.  Models and supports organization’s goals and values; adapts to changing conditions; demonstrates persistence and overcomes obstacles. 

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Demonstrated understanding of Lean principles and improvement strategies such as Value Stream Mapping, Just-In-Time, Demand Flow, Single Piece Flow, Five S’s, Visual Management, Total Productive Maintenance, Continuous Improvement Process, Kaizen, SPC, Six Sigma and Communication Tools, and Statistical Problem Solving. 

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Excellent communication skills to lead and support empowered employees in a team environment. Requires the ability to organize and direct functions under his/her direct control, as well as within a matrix reporting structure.   

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Strong project and budget management skills to guide and implement business unit plans and monitor performance to plan. Ability to prioritize, balances, and manage multiple efforts with strong results/goal orientation.  Agility and personal adaptability with the ability to successfully management multiple priorities with a high sense of urgency in a rapidly changing environment. 

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Solid analytical skills and solution-driven thinking.  Able to use large amounts of data to make strategic decisions. Passion for data, analysis, trends, reporting and technology. Ability to read and interpret documents.  Ability to write clearly and informatively routine reports, correspondence, and designs work flows and procedures.  Presents numerical data effectively. 

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Demonstrated lean manufacturing and improvement strategy development and implementation. Displays original thinking and creativity; Meets challenges with resourcefulness; Generates suggestions for improving work. 

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Identifies and resolves problems in a timely manner; develops alternative solutions; works well in a group problem solving situations; presents ideas and information in a manner that gets others' attention; displays willingness to make decisions; exhibits sound and accurate judgment; supports and explains reasoning for decisions includes appropriate people in decision-making process. 

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Ability to communicate effectively across mediums, audiences, and situations. Builds bridges and connections. Is easy to approach and talk to; is a good listener; relates well to all people throughout the organization. Is widely trusted; is seen as a direct, truthful individual; keeps confidences; admits mistakes. Follows through on commitments.  Honest and candid. 

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Demonstrated factory lean transformation capability - A success pattern that demonstrates steadily expanding scope and depth of responsibility and continuously improved personal, team and organizational outcomes. 

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Broad tactical & strategic “bandwidth”, i.e., the ability to successfully manage multiple and/or rapidly changing priorities. Learns quickly when facing new problems; a relentless and versatile learner; open to change; strives for continuous improvement of self and processes. 

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The ability to build and sustain high-performance teams through internal and external recruitment, retention and development of superior talent. Enjoys working hard; is action oriented and full of energy; enjoys challenges; drives for results. Versatility, flexibility and a wiliness to work within constantly changing priorities with enthusiasm. 

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The ability to lead by example and effectively coaches and mentors while demanding, and receiving, exceptional commitment and outstanding results. 

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Expert knowledge of JDE / MRP, Access, Word, Excel, Power Point, Visio, Project, and other applicable tools.

OTHER:

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US Persons Only (US citizens, lawful permanent residents, refugee or asylee – all require proper identification and documentation).

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Approximately 10% travel required.

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Physical and Environmental Requirements:  While performing the duties of this Job, the employee is regularly required to talk or hear. The employee is frequently required to stand and sit. The employee is occasionally required to walk and reach with hands and arms. The employee must occasionally lift and/or move up to 20 pounds. Specific vision abilities required by this job include close vision and color vision.

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Work environment includes front-office and manufacturing.  The noise level in the work environment is usually moderate.

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Pre-Employment Verifications:  Must pass background and reference checks, drug screen, and physical examination prior to employment. 

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We are an E-Verify Participant.

CIRCOR Aerospace, Inc. business offer a competitive and comprehensive benefits package, including:  medical, dental, vision, 401(k), and tuition reimbursement.   

CIRCOR Aerospace, Inc. is an Equal Opportunity Employer.  M/F/D/V 

For immediate consideration, please apply online and submit your resume to www.circor.catsone.com/career

Click here for a pdf version of this job description.

 

Cardinal Health

At Cardinal Health, we’re developing the innovative products and services that make healthcare safer and more productive. Join a growing, global company genuinely committed to making a difference for our customers and communities. 

Click here to visit their website for updated job listings that are currently available throughout their company.

Benefits:
Cardinal Health offers a competitive compensation and benefits package including 401K plan and an employee stock purchase plan. Pre-employment drug and background screening are required for all positions. 

More information about the company may be found at www.cardinal.com
We are an Equal Opportunity Employer M/F/D/V
Diversity Works Here.

Ceradyne, Inc.

Ceradyne, Inc. ( http://www.ceradyne.com ), based in Costa Mesa, California, is an ISO-certified company founded in 1967 to manufacture advanced technical ceramics for the defense, automotive, industrial, energy, medical, and electronic markets. Principal products include ceramic/composite ballistic armor, diesel engine cam rollers, oil field equipment components, translucent orthodontic brackets, and equipment components for semiconductor processing. Ceradyne serves global markets with manufacturing facilities in the United States, Canada, Europe and Asia.

As a rapidly growing publicly traded company (CRDN) we offer competitive compensation including a lucrative bonus plan, an environment that respects work/life balance, and a comprehensive benefits package.   

Click here to visit their website for updated job listings that are currently available throughout their company.

 CERADYNE IS PROUD TO BE AN AFFIRMATIVE ACTION EMPLOYER.  WE STRONGLY ENCOURAGE FEMALES, MINORITY, DISABLED, AND VETERAN APPLICANTS TO APPLY.  

Company: Boeing, Long Beach CA

This company has a website for job listings click below to search for a career with them!

Boeing Job Search

 

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Jobs listed here remain posted for a 2 month period.  If your position has not been filled by the end of that time span please contact us to keep it posted for a determined amount of time.