-
Quality Inspector. San Marcos, TX
-
Advanced Quality Engineer Supervisor. Midwest
-
Validation Manager.
Midwest
-
Validation
Engineer. Midwest
-
Quality
Assurance Engineer. Midwest
-
Quality Engineer. Austin, TX
-
Quality Engineer. San Marcos, TX
-
SQA,
Engineer IV. Austin, TX
-
Leader, Quality & Patient Safety.
Milwaukee, WI
-
Contract Quality Systems
Professional Medical Device. Austin, TX
-
Technical Writer. Austin, TX
-
Quality
Manufacturing Engineer.San
Antonio, TX
-
Director
of Quality and Risk Management. Killeen/Fort Hood, Texas
area
Job Title: Quality Inspector
Requisition Number: 10103
Functional Area: Quality
Work Location: Aerostructures - San
Marcos
Job Description Summary:
-
Performs first article
inspections of new designs and significant changes to
existing engineering configuration in accordance with
company policies & procedures
-
Reads and comprehends
technical documents and blue prints.
-
Identifies and
understands the working characteristics of all types of
aviation detail fabrication/sheet metal manufacturing &
processing.
-
Understands the
interaction between manufacturing/production and quality
systems.
-
Performs or assists in
technical investigations and research to establish
standards and methods for quality control of processes,
materials, parts and assemblies.
-
Assists in providing
formal written responses for non-conformances discovered
by customers and, or auditors
-
Identifies and documents
non-conformances (both hardware & non-hardware related)
and initiate and/or process internal/external rejection
documents.
-
Performs surveillance
audits on processes and procedures for inspection and
fabrication of hardware.
-
Assists in establishing
procedural control, audit and monitor for compliance
-
Participates in team
decision making and problem solving, actively supporting
the Goodrich People Philosophy and a 'Lean' environment.
-
Applies knowledge of
quality principles and techniques in support of the
business objectives of the organization and specific
company goals
-
Maintains quality records
in accordance with company policies and procedures.
-
Assists in the
development and maintenance of departmental metrics
-
Assists in conducting
process capability and gage R&R studies
-
Performs other duties as
assigned
-
EOE/AA/ADA
Basic Qualifications:
-
Knowledgeable of
manufacturing/assembly specifications and high tolerance
dimensions
-
Knowledge of
non-destructive testing
-
Knowledge of thermal
processing / monitoring
-
Knowledge and experience
in the use of precision measuring equipment and
familiarity with calibration requirements
-
Knowledge of windows
based software
-
Ability to communicate in
writing and orally
-
Ability to maintain
composure during stressful situations
-
Ability to establish and
maintain effective relationships with internal/external
customers
-
Ability to make good
decisions based upon a mixture of analysis, experience,
and judgment
-
Ability to understand
tooling philosophy (detail & assembly)
-
Ability to read and
interpret blue prints and specifications
-
Ability to assist in
writing and rewriting of local policies & procedures
-
High school diploma or
equivalent plus 3 years experience in a manufacturing
environment. ISO9000 type program experience preferred.
Must meet VALPAR assessment criteria to qualify for
interview.
-
EOE/AA/ADA
% Travel Required: 0%
Qualified and
interested?
Please
complete your on-line job application by clicking
here. Additional information regarding careers at
Goodrich can be found
here.
Posted: 07.11.10
Position Title: Advanced Quality
Engineer Supervisor (20361)
Degree Required:
BS Degree Engineering
Required Years of Experience:
5+ years
Industry: Medical
Device
Location: Midwest
Job
Description:
This person will supervise a
team of engineers whose focus is to collaborate with
Marketing, R&D and Operations to deliver best in class new
products to market.
Responsibilities:
-
The successful candidate
will have the opportunity to:
-
Educate the Advanced
Quality Engineering team and R&D on the use of risk
management tools, statistical methods, and design and
process control activities.
-
Help guide the AQE team
and R&D through internal quality systems to ensure that
products are developed in compliance to those procedures
as well as the requirements of the FDA, ISO and other
regulartory bodies.
-
Review and evaluates
project documentation for compliance.
-
Develop, Coordinate,
implement and maintain Quality systems for new products
and acquisitions.
-
May conduct internal
Quality system audits and be involved in CAPA projects.
-
Coaches and develops the
Advanced Quality Team and also evaluates performance.
Requirements:
This opportunity requires a
BS Degree in Engineering with 5+ years of experience in
quality engineering role or an engineering role in a
regulated environment. Also 2-4 years as a Supervisor or
Manager of a QA/RA function and have working knowledge of
FDA, ISO regulations and standards. ASQ Certifications
(CQE, CRE, CQM or CSSBB) a plus. Working knowledge of
Risk Analysis, GD&T, SPC, Root Cause Analysis, Statics and
practical application. Great interpersonal skills
along with demonstrated effective managerial skills.
Quality Assurance knowledge and understanding along with
Process Validation experience as well.
Join a global leader in their industry!
Company growth is based on an unparalleled variety of
high-quality, innovative products/services that create
cost-effective solutions and improve people’s lives.
Please contact me for additional information
regarding this excellent opportunity and company! If
this is not the time for you to make a career move, please
share with individuals you feel may be qualified. I
truly appreciate your assistance in networking with me!
Danielle R. DeSmit | Recruiter
| Professional Outlook, Inc.
616.796.2298
danielle@professionaloutlook.com
Please visit
www.professionaloutlook.com for additional positions
that are currently available.
Posted: 07.11.10
Position Title: Validation Manager
(20358)
Degree Required:
Bachelors Degree in Mechanical, Electrical or Industrial
ONLY
Required Years of Experience:
7+ years
Industry:
Medical Device
Location:
Midwest
Job
Description:
The
Validation Manager will participate in and lead the
development, implementation and adherence to validation
procedures (computer system, equipment, utilities, cleaning
and process)
Responsibilities:
The
successful candidate will have the opportunity to:
-
Own and improve the validation quality
system.
-
Provide subject matter expertise for
regulartory inspections.
-
Represent validation in cross-functional
meetings/projects.
-
Select, develop, and lead personnel to
ensure department objectives are met.
-
Manage the department budget.
-
Coordinate relationships with vendors and
contractors.
Requirements:
This
opportunity requires a Bachelors Degree in Mechanical,
Electrical or Industrial and have 3+ years of leadership
experience. Must also have 5+ experience with writing,
executing and reporting (IQ/OQ/PQ) and 7+ years of cGMP/FDA
regulated industry experience as well.
Join a global leader in their industry!
Company growth is based on an unparalleled variety of
high-quality, innovative products/services that create
cost-effective solutions and improve people’s lives.
Please contact me for additional information
regarding this excellent opportunity and company! If
this is not the time for you to make a career move, please
share with individuals you feel may be qualified. I
truly appreciate your assistance in networking with me!
Danielle R. DeSmit | Recruiter
| Professional Outlook, Inc.
616.796.2298
danielle@professionaloutlook.com
Please visit
www.professionaloutlook.com for additional positions
that are currently available
Posted: 07.11.10
Position Title: Validation Engineer
(20357)
Degree Required:
Bachelors Degree in Mechanical, Electrical or Industrial
ONLY
Required Years of Experience:
5+ years
Industry:
Medical Device
Location:
Midwest
Job
Description:
The
Validation Engineer will participate in and lead the
development, implementation and adherence to validation
procedures (computer system, equipment, utilities, cleaning
and process)
Responsibilities:
The
successful candidate will have the opportunity to:
-
Develop/Write/Document/Execute protocols
and final reports (IQ/OQ/PQ).
-
Review/approve protocols and final
reports (IQ/OQ/PQ).
-
Represent validation in cross-functional
meetings/projects.
-
Coordinate and approve vendor protocols.
Requirements:
-
This
opportunity requires a Bachelors Degree in Mechanical,
Electrical or Industrial and has 5+ years of experience.
-
Must
have 5+ experience with writing, executing and reporting
(IQ/OQ/PQ) and 5+ years of cGMP/FDA regulated industry
experience with good understanding of process risk
analysis.
Join a global leader in their industry!
Company growth is based on an unparalleled variety of
high-quality, innovative products/services that create
cost-effective solutions and improve people’s lives.
Please contact me for additional information
regarding this excellent opportunity and company! If
this is not the time for you to make a career move, please
share with individuals you feel may be qualified. I
truly appreciate your assistance in networking with me!
Danielle R.
DeSmit | Recruiter | Professional Outlook, Inc.
616.796.2298
danielle@professionaloutlook.com
Please visit
www.professionaloutlook.com for additional positions
that are currently available.
Posted: 07.11.10
Position Title: Quality Assurance
Engineer (20303)
Degree Required:
BS Mechanical Engineering/Electrical Engineering ONLY
Required Years of Experience:
2-3 years
Industry:
Medical Device
Location:
Midwest
Responsibilities:
The
successful candidate will have the opportunity to:
-
Develop
the next generation of EMS and Evacuation equipment
-
Collect, interpret and determine the root cause of
failures
-
Identify and track potential product and process risks
-
Assist
and develop process controls
-
Prepare
product and operations for transition.
Requirements:
-
This
opportunity requires a Mechanical or Electrical
Engineering degree along with Six Sigma Black Belt
Certification (or equivalent certification).
Working knowledge of Quality System Regulation 21 CFR
Part 820, cGMP and FDAs guidance on design controls.
Must have previous experience with developing,
transferring and/or launching a new product into
production and conducting Risk Management activities for
new and/or existing products.
-
ISO-9000 a plus as well!
Join a global leader in their industry!
Company growth is based on an unparalleled variety of
high-quality, innovative products/services that create
cost-effective solutions and improve people’s lives.
Please contact me for additional information
regarding this excellent opportunity and company! If
this is not the time for you to make a career move, please
share with individuals you feel may be qualified. I
truly appreciate your assistance in networking with me!
Danielle R. DeSmit | Recruiter
| Professional Outlook, Inc.
616.796.2298
danielle@professionaloutlook.com
Please visit
www.professionaloutlook.com for additional positions
that are currently available.
Posted: 07.11.10
Specific Job Duties:
This Quality Engineer
position will be responsible for implementation of quality
system improvements/deployments/audits as well as supporting
the quality operations activity. Job responsibilities may
include the following:
-
Identification and
containment of suspect material, characterization of
device parametric performance and disposition of
reliability and quality issues
-
conduct wafer level
analysis and interface with process engineering and
package/assembly to resolve quality signals
-
system deployment of
medium to large-scale projects that are cross-functional
in nature and have visibility to company executives
-
drive quality indices to
achieve established business objectives
-
coordinate and lead
activity in response to daily operations issues and
quality concerns to achieve root-cause countermeasures
and recurrence prevention
-
perform internal audits
of all SAS departments to ensure SAS is in compliance
established specs and standards
-
interact with
engineering, manufacturing, services group counterparts,
and executives to help achieve quality goals
-
analyze and make
recommendations to help improve quality indices for each
department’s processes and programs
Skills, Software
Knowledge, Toolsets:
-
Knowledge of
semiconductor fab processing and yield/reliability
mechanisms required.
-
A high level of
self-motivation and strong communication skills (written
and presentation) required.
-
Must be able to work and
navigate with the following systems: document control,
statistical process control, manufacturing execution
systems, data mining and analysis applications, process
change/improvement experiment design and execution.
-
Working knowledge of all
Microsoft Office products is required
-
Two to eight years of
semiconductor engineering experience preferred.
-
Detailed understanding
and experience with SPC and process control systems
preferred.
Specific Certifications:
-
BS degree in engineering,
materials science or related field preferred, equivalent
semiconductor experience may be considered.
-
Lean/6Sigma/statistical
training preferred.
-
Working knowledge of
TS16949 standard is a plus
Qualified and Interested?
Send your resume to
s.english@samsung.com
in pdf or word format.
Posted on 06.29.2010
Job Title: Quality
Engineer
Requisition Number: 9105
Functional Area: Quality
Work Location: Aerostructures - San Marcos
Job Description Summary:
-
Provide Quality interface
and expertise between the organization and its customers
to proactively assure that their needs and expectations
are understood and satisfied. This includes contract
review/flow-down, the complaint management process, and
the implementation of the corresponding corrective /
preventive actions.
-
Provide support to the
Supply Chain Management organization relative to the
collection and analysis of Supplier Quality data as well
as provide Quality interface, expertise and support to
the Plant’s/SBU’s suppliers and partners. This includes
the preparation of reports of supplier performance used
to give feedback to suppliers and to the organization.
-
Provide expertise in
Quality Assurance and process improvement tools and
methods to targeted functions of the organization to
support them in their continuous improvement activities
Execute the initiatives of the organization in the
development, implementation and improvement of the
appropriate Quality Management Systems throughout the
operation, with all the documentation required. This
includes providing advanced quality planning support in
the development and launch of new products, processes
and services.
-
Participate in the
internal Quality System Audit program for the
organization. Develop, implement and audit of inspection
and test plans, standards and acceptance criteria, and
procedures / work instructions. Facilitate the
Investigation and elimination of causes of quality
problems and follow up on corrective actions.
-
Develop and analyze
statistical data and product / process performance to
recommend and implement improvements in targeted areas
of the organization.
-
Provide support in the
way of development and evaluation of process capability,
process control plans, analysis of out-of-control
conditions and process audits with the objective of
improving process performance and capability.
-
Participate in all
aspects of product development and launch activities
throughout the organization. Efforts should primarily be
targeted at the identification of customer expectations,
manufacturing and test support, reliability analysis,
design reviews, evaluation of test programs, material
testing and inspection and management of quality costs.
EOE/ADA/AA
Basic Qualifications:
-
Analytical Problem.
Solving Understands problem solving methods – i.e. 8D,
root cause analysis, Apollo etc. – and the associated
statistical tools used to analyze problems.
-
Supplier Quality.
Understands many aspects of managing and assuring
supplier quality to achieve best-in-class supplier
quality, delivery and service.
-
New Product Development
and Launch. Basic knowledge of the key phases and
requirements of an effective new product development and
launch system – i.e. APQP, Stride, etc. – and has basic
knowledge of the associated tools such as PFMEA, Control
Plans, Characteristic Matrix, Gage Capability, Process
Capability, Process Flow, Preventive Maintenance,
Machine Runoff, etc.
-
Quality Technologies.
Understands some of the appropriate ASQ Body of
Knowledge (BOK) (CQE, CQA, CRE, CPA) and understands the
corresponding concepts and tools.
-
Quality Management
Systems. Moderate understanding of the standards,
implementation and certification process of Quality
Management Systems such as AS/EN9100, ISO-9001, or any
other industry-specific standard or regulation is
required. Moderate understanding of the requirements of
customer-specific Quality System certification programs.
-
Continuous Improvement.
Knowledge of the tools and techniques of Lean
Manufacturing such as Value Stream Mapping, 5S -
Workplace Organization, Continuous Flow Manufacturing,
Set-up Reduction, Total Productive Maintenance, Mistake
Proofing, etc.
-
Cost of Quality.
Understanding the concept of Cost of Quality and
specifically of the Cost of Non-Conformance. Uses Cost
of Quality report to identify opportunities for
improvement and waste reduction. Ability to solve
problems of limited scope and complexity
-
BS degree in
Engineering/Science/Engineering Technology/Quality plus
a minimum of at least one year of related experience.
-
Six Sigma Green or Black
Belt certification required.
EOE/ADA/AA
%Travel Required:
< 10%
Qualified and
interested?
Please
complete your on-line job application by clicking
here. Additional information regarding careers at
Goodrich can be found
here.
Job Title: Quality
Engineer
Requisition Number: 9106
Functional Area: Quality
Work Location: Aerostructures - San Marcos
Job Description Summary:
-
Provide Quality interface
and expertise between the organization and its customers
to proactively assure that their needs and expectations
are understood and satisfied. This includes contract
review/flow-down, the complaint management process, and
the implementation of the corresponding corrective /
preventive actions.
-
Provide support to the
Supply Chain Management organization relative to the
collection and analysis of Supplier Quality data as well
as provide Quality interface, expertise and support to
the Plant’s/SBU’s suppliers and partners. This includes
the preparation of reports of supplier performance used
to give feedback to suppliers and to the organization.
-
Provide expertise in
Quality Assurance and process improvement tools and
methods to targeted functions of the organization to
support them in their continuous improvement activities
Execute the initiatives of the organization in the
development, implementation and improvement of the
appropriate Quality Management Systems throughout the
operation, with all the documentation required. This
includes providing advanced quality planning support in
the development and launch of new products, processes
and services.
-
Participate in the
internal Quality System Audit program for the
organization. Develop, implement and audit of inspection
and test plans, standards and acceptance criteria, and
procedures / work instructions. Facilitate the
Investigation and elimination of causes of quality
problems and follow up on corrective actions.
-
Develop and analyze
statistical data and product / process performance to
recommend and implement improvements in targeted areas
of the organization.
-
Provide support in the
way of development and evaluation of process capability,
process control plans, analysis of out-of-control
conditions and process audits with the objective of
improving process performance and capability.
-
Participate in all
aspects of product development and launch activities
throughout the organization. Efforts should primarily be
targeted at the identification of customer expectations,
manufacturing and test support, reliability analysis,
design reviews, evaluation of test programs, material
testing and inspection and management of quality costs.
EOE/ADA/AA
Basic Qualifications:
-
Analytical Problem
Solving - Understands problem solving methods – i.e. 8D,
root cause analysis, Apollo etc. – and the associated
statistical tools used to analyze problems.
-
Supplier Quality.
Understands many aspects of managing and assuring
supplier quality to achieve best-in-class supplier
quality, delivery and service.
-
New Product Development
and Launch. Basic knowledge of the key phases and
requirements of an effective new product development and
launch system – i.e. APQP, Stride, etc. – and has basic
knowledge of the associated tools such as PFMEA, Control
Plans, Characteristic Matrix, Gage Capability, Process
Capability, Process Flow, Preventive Maintenance,
Machine Runoff, etc.
-
Quality Technologies.
Understands some of the appropriate ASQ Body of
Knowledge (BOK) (CQE, CQA, CRE, CPA) and understands the
corresponding concepts and tools.
-
Quality Management
Systems. Moderate understanding of the standards,
implementation and certification process of Quality
Management Systems such as AS/EN9100, ISO-9001, or any
other industry-specific standard or regulation is
required. Moderate understanding of the requirements of
customer-specific Quality System certification programs.
-
Continuous Improvement.
Knowledge of the tools and techniques of Lean
Manufacturing such as Value Stream Mapping, 5S -
Workplace Organization, Continuous Flow Manufacturing,
Set-up Reduction, Total Productive Maintenance, Mistake
Proofing, etc.
-
Cost of Quality.
Understanding the concept of Cost of Quality and
specifically of the Cost of Non-Conformance. Uses Cost
of Quality report to identify opportunities for
improvement and waste reduction.
-
Ability to solve problems
of limited scope and complexity BS degree in
Engineering/Science/Engineering Technology/Quality plus
a minimum of at least one year of related experience.
-
Six Sigma Green or Black
Belt certification required.
EOE/ADA/AA
% Travel Required:
< 10%
Qualified and
interested?
Please
complete your on-line job application by clicking
here. Additional information regarding careers at
Goodrich can be found
here.
Posted: 06.24.10
Company Name: Polycom Inc.
Job
Title:
SQA Engineer IV
Req
Number:
10567
Description:
* Execute detailed test scenarios from
written test plans
* Analyze test results and report findings
* Write detailed defect reports
* Use diagnostic hardware and software tools
* Set up and configure networking,
audio/visual and computer equipment
* Write Automated and Manual test cases
* Mentor more junior testers
* Work directly with development to create
test requirements for new features
Skills:
* Excellent written and verbal communication
skills required
* Proficiency with Unix/Linux a plus
* Networking/telecommunications skills (IP,
ISDN, telephony) strongly desired
* Programming/scripting (C/C++/scripting
languages) skills a plus
* Audio/visual skills a plus
Experience:
* 8 years job experience software/hardware
testing (strongly desired), hardware/software technician,
technical support or information services/IT
Education:
* 4-year degree required
Qualified and interested? Please
submit your resume in MS Word or Adobe .pdf format to: Jeff
Polo Polycom Staffing Team
jeff.polo@polycom.com
Posted 06.15.10
The Organization
Children’s Hospital of
Wisconsin (CHW) is a 296-bed, private, non-profit Level I
Pediatric Trauma Center and major teaching affiliate of the
Medical College of Wisconsin. It is a part of The Children’s
Hospital & Health System (CHHS) of Wisconsin, comprised of
12 entities throughout the state providing medical care,
social services, fund-raising and research. Last year,
23,000 infants, children and adolescents were admitted and
379,000 were seen in the hospital’s specialty outpatient
clinics and urgent care sites. The Emergency Department
treated 60,000 children and 14,628 surgical procedures were
performed. Care is provided to children from Wisconsin,
Michigan, northern Illinois and beyond. CHHS has been
recognized by U.S. News & World Report and U.S. News Media
Group’s 2009 edition of America’s Best Children’s Hospitals
for quality. One hundred sixty-six Children’s Hospital of
Wisconsin physicians are listed in the 2009-2010 Best
Doctors in America database. (www.chw.org)
The Opportunity
-
The Leader of Quality &
Patient Safety coordinates the hospital’s quality
improvement and clinical effectiveness programs and lays
the groundwork for quality initiatives at the system
level.
-
Manages a staff of 12.5
FTEs and has budgetary responsibility for $1.5M.
-
Provides a leadership
framework for collaboration and shared accountability
for performance with physicians, patient care staff,
business and support services.
The Candidate
-
Senior-level professional
with significant experience in hospital/health system
quality improvement principles, Joint Commission
standards, safety issues and healthcare operations.
-
A Master’s degree is
required.
-
Project Management
Experience with multiple hospital entities or at the
hospital system level is essential.
-
Clinical experience as a
nurse or physician with training/experience in
epidemiology, biostatistics, public health or related
disciplines is highly desired.
-
Understanding of Quality
Initiatives on a national level.
-
Experience with
improvement methodologies such as The Improvement Model,
Six Sigma or LEAN.
-
Public speaking and/or a
history of written publications a plus.
The Community
Milwaukee, Wisconsin’s
largest city with a population of 602,000, (1M in the metro
area) lies on the western shore of Lake Michigan. The metro
area is home to thirteen Fortune 500 company headquarters,
but has managed to maintain a small town atmosphere.
Milwaukee has a number of notable performing art groups
including opera, ballet a professional symphony and several
theatre groups. Art, history and science museums attract
visitors, as do professional football and baseball teams.
Both public and private schools are excellent. (www.10best.com/Milwaukee
and
www.visitmilwaukee.org )
An attractive salary, benefit
and relocation package is offered.
If you are interested, please
contact:
Jane Fischer,
Tyler & Company
jfischer@tylerandco.com
(610) 558-6100, extension 231
All inquiries will be handled confidentially.
www.tylerandco.com
Posted 05.17.10
Our client, a medical device
company, is looking for an experienced QUALITY SYSTEMS
contractor.
Overview: Our client
is integrating two quality systems due to a company
acquisition. In addition to integrating the systems, our
client is looking to further enhance the quality systems.
The contractor will be part of a larger team and will take
direction from team leaders. Our client is looking for
someone with a drive to be hands on and get the job done.
The quality system must be compliant with current FDA and
ISO standards.
Requirements: Strong
analytical, organizational, interpersonal and communication
(written and verbal) skills. Microsoft Excel and Word
proficiency. Medical device experience. Candidate must be in
the Austin, TX area.
Term: Length of
assignment is approximately 8 months.
Send resume to
katerichards@vallonllc.com
Posted 05.07.10
Medical Device Company in
Austin, TX looking for a technical writer. This is a
contract position.
The job scope is to write
clinical and reimbursement standard operating procedures
(SOP).
If you are interested in this
position, please send a resume to Debbie St.Wrba at
dstwrba@ininc.us
Posted 05.05.10
Summary:
The Senior Manufacturing
Engineer is responsible for the management of resources to
support large-scale programs and manages medium to large
size projects for the Manufacturing Engineering Department
and Global Operations. In addition, the Senior Manufacturing
Engineer performs work that involves conventional
engineering practice but may include a variety of complex
features such as conflicting design requirements,
unconventional materials and difficult coordination
requirements.
Duties and
Responsibilities:
Responsible for organizing,
planning, monitoring, controlling and scheduling the
necessary activities of medium to large scale projects to
achieve goals. Coordinate resources between competencies
(quality, engineering, research & development,
manufacturing) to take new product design into a production
line. Leads resources and/or teams and other activities to
verify and validate new and existing manufacturing
processes. Responsible for the Installation, Operational and
Performance Qualification (IQ, OQ & PQ) activities for
various equipment and manufacturing processes. Initiates
and/or evaluates requirements and deliverables of process
changes. Given projects that involve external transition of
products out candidate will be responsible to chart the
project and manage needed resources to complete transition
successfully. May oversee or coordinate the work of
engineers, draftsmen, technicians and other positions that
assist in specific assignments when requested. Applies lean
manufacturing tools to ensure most productive methods are
utilized in production lines. Develop program plans and
track progress related to the above listed initiatives.
Attend product development meetings and provide
Manufacturing Engineering input. Reply to corrective actions
requests (CAR) for product and process related issues.
Provides Design for all desirable attributes/Design for
manufacturability (DFX/DFM) input and evaluation to product
development, support manufacturing by providing
cost-improvement alternate assembly methods. Supports the
development and training of subordinate engineers. Conforms
to, supports and enforces all Company policies and
procedures Participates in any and all reasonable work
activities as may be deemed suitable and assigned by
management.
Other Required
Qualifications:
Experience in New Product
Development Processes. Experience in Manufacturing
Processes. Demonstrated project management experience.
Experience in regulated design environments a plus –
specifically medical device development, Federal Drug
Administration (FDA) or ISO registered. Ability to deal
effectively with all employees and external business
contacts while conveying a positive, service oriented
attitude. Ability to communicate effectively, both verbally
and in writing. Ability to maintain complete confidentiality
and discretion in business relationships and exercise sound
business judgment.
Qualified and interested candidates should submit resumes in
MS Word or Adobe .pdf format to
mscherer@aerotek.com
Posted 04.26.10
|
Director of
Quality and Risk Management
Killeen/Fort Hood, Texas area |
 |
FaithSearch Partners, Inc.
has been retained to manage the search for a Director of
Quality and Risk Management for a non-profit,
faith-based hospital that provides services primarily in the
Killeen/Fort Hood, Texas area. This hospital is part of a
regional health care system and network of providers that
includes hospitals, a major teaching facility and other
health care services.
The Director serves as the
Quality Improvement leader for this 233-bed hospital that is
generating more than $105 million in net revenues annually
and employs nearly 1,200 individuals. He/She will oversee
all major quality metrics and improvement processes.
Reporting to the Chief Medical Officer, the Director leads
the Quality and Risk Management Department that has
responsibility for leading all quality initiatives. The
ideal candidate for this position is well-prepared
academically with a bachelors degree. An undergraduate
degree in nursing or other clinical area is preferred.
Previous experience as a Director of Quality and Risk
Management is desired but not required.
If you are interested in
learning more about this position, please contact Ivan
Bartolome at 913-226-0073 or
ivan@faithsearchpartners.com
Ivan Bartolome
Senior Vice President
FaithSearch Partners, Inc.
www.faithsearchpartners.com
ph. 913.226.0073 e-mail.
ivan@faithsearchpartners.com
Kansas City - Houston - Dallas - Washington
DC
Posted on 04.21.10
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