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ASQ Job Opportunities
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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
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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 |
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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.
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Maintain company compliance with FDA Quality System Regulations and ISO
13485 standards,. Experience with FDA and ISO inspections and
registration is a plus.
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Actively
participates in internal audits, management review and other activities
covered under Accellent Quality Manual, Policies and Procedures.
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Provide
customer related quality and regulatory inquiries support.
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Compiles and
writes training material and conducts training sessions on quality
control activities.
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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.
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Lead
implementation of continuous improvement project or act as subject
matter expert for SPC, FMEA, DOE, and process validations
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Lead and
provide Project Management support as needed
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Develops and
initiates standard methods for inspection, testing, and evaluations,
utilizing knowledge in related engineering fields.
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Devises
sampling procedures and designs and develops forms and instructions for
recording, evaluating, and reporting quality and reliability data.
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Performs
measurement system analysis to evaluate test and inspection equipment
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Leads
disposition of discrepant material and devises process to assess product
quality and reliability
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Monitors and
directs engineering group on calibration requirements and implementation
of systems to support equipment calibration
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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
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Directs workers
engaged in measuring, testing, and tabulating data concerning quality
and reliability
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Up to 10%
travel may be required
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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
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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
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Anyone interested,
please email resume to
rybarra@purcellintl.com |
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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 |
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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.
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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. |
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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.
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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
|
If you have a
job listing you would like to post here, please email them to John Schulz
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. |
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