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Westinghouse Electric
Company Title: Quality InspectorLocation:
Quality Inspector
Westinghouse Electric
Company LLC, Nuclear Components Manufacturing, Newington Operations, a major
supplier of components to the utility industry, is seeking qualified QUALITY
CONTROL INSPECTORS. Candidates must meet the following requirements: ·
Minimum of
five years experience as a mechanical parts inspector. Knowledge of mechanical inspection
techniques, geometric dimensioning and tolerancing,
and experience working to close tolerances in a machine shop
environment. CMM programming
capability in Zeiss Calypso software would be an
advantage. ·
Prior
certification or background in Nondestructive Testing in accordance with
SNT-TC-1A to Level II in one of the following methods: Radiography,
Ultrasonic, Magnetic Particle, Liquid Penetrant and
Visual Examination would also be an advantage. ·
A thorough
knowledge of welding, welding symbols and the ability to interpret
engineering drawings. Qualified applicants should send resume to: James Dunn Westinghouse Electric
Company Fax to: (603) 433-1060 e-mail: James.m.dunn@us.westinghouse.com Westinghouse Electric
Company is an equal opportunity employer Posted: 11/10/08 |
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BAE Systems Click
to view list of positions
Location:
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Infinity Pharmaceuticals Title: Senior Quality Assurance Specialist -GMP AuditsLocation:
Infinity Pharmaceuticals
is an innovative cancer drug discovery and development company that is
seeking to leverage its strength in small molecule drug technologies to discover,
develop, and deliver to patients first-in-class or
best-in-class medicines for the treatment of cancer and related conditions. Position Description: The Senior Quality
Assurance Specialist will work with Infinity project teams, contract manufacturing
organizations, and contract testing laboratories to move products from
research to preclinical to clinical trials in support of the company’s drug
discovery and development efforts. The Senior Quality Assurance
Specialist will perform internal and external audits to ensure the Infinity
as well as GLP, GCP and GMP vendors comply with applicable regulation.
This position will also back up other department members with batch record
and study report review as well as writing and revising SOPs
·
Performing
GMP, GCP and GLP vendor audits and setting audit schedules ·
Review and
release clinical trial material. ·
Work closely
with contract manufacturing organizations and contract testing laboratories
to ensure cGMP compliance. ·
Quality planning
for moving products from research to preclinical to clinical trials including
specification development, batch record creation/approval, and test method
validation. ·
Writing and
revising SOPs Requirements: ·
Minimum of a BS degree in a scientific discipline, preferably
chemistry ·
5-6 years of
Quality Assurance experience in regulated manufacturing, laboratory and/or
clinical environments ·
Ideal
candidates will be flexible and willing to travel up to 50%. ·
Proficiency in
auditing at least one GXP function is a core requirement. ·
2-3 years
auditing experience in either GMP, GCP or GLP.
Experience in multiple disciplines in preferred ·
Thorough
knowledge and understanding of current Good Manufacturing Practices (GMP),
and Good Laboratory Practices (GLP) guidelines ·
Good
Clinical Practices (GCP) experience a plus ·
Strong
written and verbal communication skills, interpersonal skills, technical writing skills, and the
ability to work well in a team environment Infinity
offers an outstanding benefits package and is an EOE. Posted:
10/24/08 |
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Covidien Title: Quality Engineers
Location:
The
Respiratory and Monitoring Solutions Business Group is a $1.2 billion dollar
division of Covidien, formerly Tyco Healthcare. RMS
systems are used to monitor, diagnose and treat respiratory disease and sleep
disorders, and provide life sustaining ventilation and oxygen support for
patients. We are currently recruiting
for the following positions: SOFTWARE QUALITY ENGINEER - Boulder, CO Corp HQ – relo provided Would you - Like to
leverage your expertise in software testing and with the software development
process? Move
into software quality to help to set up a more efficient and effective design
processes? Have a
significant impact on product quality? Grow
your career and join a team that is working to get it right from the start –
refine the processes, redefine the activities, and make sure the proper events occur at the
right time? Share
your knowledge and support the product design team providing guidance,
mentoring and training? Then join Covidien
Respiratory and Monitoring Solutions as a Software Quality Engineer! Position
Summary: Responsible
for ensuring that the software used as part of our medical devices and
products is developed according to good design practices. Minimum Requirements: BS EE, CS, or CE 3+ yrs in a software quality engineering or software test
role dealing with software that is part of a medical device, or a product for
a highly regulated industry i.e. aerospace, automotive, etc. MED DEVICE NOT
REQUIRED Working knowledge of product risk assessment,
requirements management and tracing, defect tracking, configuration
management techniques, and how they are applied in the software development
lifecycle Understanding of current Software Quality techniques
and software industry standards (e.g. ISO, IEEE, CMMI), and their impact on
internal procedures, software quality, safety and efficacy of products Working
knowledge of C, C++, and LabVIEW SR. QUALITY ENGINEER - Boulder, CO Corp HQ – relo provided Position
Summary: Provide
quality engineering support in the design and development of medical device
products, and facilitate the application of design controls. Translate Quality Standards into processes
and procedures and apply these to the new product design process. Minimum
Requirements: BS in an engineering
discipline, EE preferred 5+
yrs of quality engineering experience Skilled
in test plan development and root cause failure analysis Skilled in statistical
methods, including ANOVA, statistical process control, sampling plans, gauge
R&R, and design of experiments. Familiar with reliability
analysis and test methods Familiar with
ISO 14971 or strong experience in risk evaluation techniques,
such as FMEA and/or fault tree analysis CQE certification desirable Contact: For more information about these opportunities, go to: www.covidien.com/careers. Pull up jobs for Covidien is an Affirmative Action / Equal Opportunity Employer. Posted:
8/22/08 |
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The Timken Company Title: Quality Engineer - 0800584
Location:
Job Description Primarily responsible for auditing,
analyzing, and reviewing Customer specification versus internal processes
throughout the Company to ensure compliance to internal specifications,
standards, and quality management system practices, while meeting Customer
expectations and our commitments to Customers. 1. Contract review for Customer Quality
Requirements, including print and specification review that flows down these
requirements for the design and manufacture of our products 2. Internal auditing for compliance and
effectiveness of business and manufacturing processes 3. Ability to recommend and implement
process changes to improve quality and productivity from audits and reviews
using Lean/Six Sigma tools and techniques to E1 level(Green
Belt). 4. Interfaces with the customer service,
sales team and Customer to resolve issues related to compliance to
specifications or product quality in a timely manner.
5. Monitoring and evaluation of data
metrics to ensure that customers are satisfied with HPC performance. Contact:
Apply
online for this position. Posted:
8/21/08 |
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The Timken Company Title: Quality Engineer - 0800466
Location:
Job Description Be the quality member of a cross functional area team
resolving quality issues in support of team objectives including but not
limited to: A. On time delivery goals B. Past due reduction goals C. Scrap reduction goals 1.
Be part of a cross functional area team resolving quality issues in support
of Keene KPI goals and objectives, by reviewing, analyzing, and creating
improvement plans based on e-PIR data. 2.
Support Continuous Improvement activities utilizing Process Capability
studies, Machine capability studies, Gage R&R studies and other
statistical problem solving tools. 3. Be
part of the implementation of Operator Quality Certification program within
the area, including assessing, training and mentoring of the operators. 4.
Support the integrity of the quality system used in the facility. 5.
Utilize 8D techniques to investigate root cause analysis and perform
effective positive corrective action. 6.
Support efforts to resolve and eliminate nonconformances. 7.
Support L6S teams, Kaizen events and be knowledgeable with flow lines. Contact:
Apply
online for this position. Posted:
8/21/08 |
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The Timken Company Title: Supervisor, Mfg Inspection - 0800588
Location:
Job Description To supervise, organize and track shift coverage of
inspectors for supporting receiving inspection, component inspection, and
production. To provide leadership and direction to all associates within
those areas. In addition to existing supervisor duties, this person will
lead, coach, direct and support inspection processes, SPC, operator quality
certification, support cost reduction, and be responsible for scrap and
rework (PIR) data collection and Pareto analysis. 1)
Maintain the integrity of the quality systems use in the production facility. 2)
Maintain high level of work throughout the Inspection Department with all
resources to assure lowest costs, highest quality and continuous throughput. 3)
Participate in continuous improvement efforts within the Quality Dept. 4)
Lead efforts to resolve and eliminate nonconformances. 5)
Improve safety awareness. 6)
Maintain a well cross-functional team to support various quality functions. 7)
Hire, train, discipline, and develop associates in the inspection areas. 8)
Maintain operating budgets, support Quality KPI metrics, and establish
operating procedures. 9)
Interact with internal and external customers and suppliers as needed, and to
provide supportive information to managers for continuous improvement
opportunities. 10)
To complete all required and assigned tasks accurately and on time. Contact:
Apply
online for this position. Posted:
8/21/08 |
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The Timken Company Title: Manager, Gauging Systems - 0800375
Location:
Job Description 1. Supervise the Gage Service and Metrology Department;
consisting of Inspectors, Technicians, and Metrologists. Contact:
Apply
online for this position. Posted:
8/21/08 |
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