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Employers – Posted Resumes
Employees - Jump to Job Postings Listed Below:
Quality Technician |
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Supply and Compliance Quality Engineer |
NOTE: Members may now submit their resume to be posted on this site. If you are interested in posting your resume, please contact Brian Krady
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Attention: All jobless ASQ members |
Lancaster County Provides a service to all unemployed people. Its called JOB CLUB! They can be reached by calling 397-4159.
They provide training to get a job. The training includes Resume writing, Cover letters, cold calling, thank you letters, Interview skills.
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Please feel free to contact me if you have any questions or forward your resume if you would like it posted on the site!
Brian Krady (ASQ Placement Chair)
Vice
President of Quality
LOCATION: 400 + bed hospital in
DESCRIPTION:
Summary:
The position reports to the CEO and oversees Quality, Infection Control, and Risk Management. Incumbent will oversee a staff of 10, including IC Director and Director of Risk.
8-10 years of hospital experience is required. Salary is very competitive, with bonus potential. Relocation is provided, with possible sign on bonus.
Lisa Regan-Thierry
President
Edwards
& Greer Healthcare Partners
Direct:
401- 451-4179
E-mail: lisa@edwardsandgreer.com
Quality
Technician
Unilife
Medical Solutions, Inc. is a medical device company in
Job Summary:
Quality
Technicians evaluate product and component drawings and documentation, perform
product functional performance testing, inspect components and finished
products, measure process performance, record data and prepare formal reports
regarding nonconforming product or processes in support of and under the
direction of quality engineers or the Quality Control
Manager.
Education/Experience Required:
High School Diploma
or equivalent GED required; 2 years of higher education from a college,
university, or technical school, or 2 years experience in a regulated industry
performing duties related to process or product quality preferred. Must
be familiar with basic quality terms, definitions, and concepts and basic
statistical terms and techniques, including how to record and plot data and how
to recognize out-of-control conditions. Must have an understanding of
types of measurement, measurement terminology and the different types of
measurement scales and must be able to apply basic inspection and testing
techniques, determine sample size for lots, and pull random samples. Must
be able to read and interpret blueprints (drawings), including geometrical
dimensioning and tolerancing (GD&T) and know definitions of critical, major
and minor characteristics. Must be skilled in the proper handling and use
of various types of inspection, measurement, and test equipment.
Physical/Mental Demands of Job:
Quality Technicians must be able to read and understand confidential product drawings, specifications, and process procedures in order to perform the duties of the occupation. Quality Technicians are required to identify and investigate nonconforming product and determine and communicate its scope and work directly with other personnel within the Company to ensure quality of product. This position involves extensive standing, regular lifting and carrying of up to 40 pounds, and visual inspection, which requires excellent visual acuity. The ability to work in a clean room environment is an essential job function, as is the ability to communicate effectively orally and in writing with the entire workforce. The ability to perceive all aspects of the work environment, product and component samples and documentation is essential. This position requires attention to detail, excellent time and document management skills and the drive to complete and follow-through for completeness. Must be able to maintain self-control in challenging circumstances and be reliable in attendance and punctuality.
Apply with resume in word format to: Unilife.com
EEOC employer with competitive wages and benefits.
QC
Supervisor
Unilife
Medical Solutions, Inc. is a medical device company in
Job Summary:
The QC
Supervisor Level 2 is responsible for performing a wide variety of tasks
involving supervision of incoming, in-process and finished product inspection
of raw materials and assembled medical devices. He/she is responsible for
executing the QC plan set by the QC Manager for his/her shift. This
includes inspection equipment set-up and change-overs, timely inspection of
materials, directing QC technicians, and supervising/conducting quality checks.
As required, he/she will work along-side inspection technicians in work that
requires manual dexterity, visual acuity and speed to perform the task at the
required rate. He/she is also responsible for ensuring that all QC
technicians follow specific written work instructions and providing training
and corrective feedback, when required. He/she will record
quality-related data and information. Duties will also include assuring
QC areas are properly maintained, inspection equipment is within calibration
and that areas are cleared for inspection to avoid mix-ups
Education/Experience Required:
High school diploma or GED required. 10 years on-the-job training and experience as a supervisor of QC employees required. College degree preferred. Computer skills in MS office products, including Word, EXCEL and database programs are required. Familiarity with and certification in Six Sigma, LEAN manufacturing or other vigorous quality control programs are highly desirable. Applicable ISO and FDA experience is highly desirable. QC Supervisors are responsible for providing leadership on shift to QC employees, handling emergency inspection needs and planned equipment change-overs, performing quality assurance functions, handling emergencies calmly, resolving conflicts among QC employees and enforcing performance standards, as well as working with QC employees in work that involves visual and physical inspection. QC Supervisors must be able to read and understand all written instructions, communicate well with others, and have excellent vision and manual dexterity. The ability to work in a clean room environment is an essential job function, as is the ability to communicate effectively orally and in writing with the entire workforce. The ability to perceive all aspects of the work environment, product and component samples and documentation is essential. This position requires attention to detail, excellent time, people and document management skills and the drive to complete and follow-through for completeness. The ability to handle multiple priorities in a fast changing work environment is essential, as is positive interaction with others and reliable attendance.
Apply with resume in word format to: Unilife.com
EEOC employer with competitive wages and benefits
Supply and
Compliance (SC) Quality Engineer
Unilife Medical
Solutions, Inc.
is a medical device company in
Job Summary:
The Supply and Compliance Quality Engineer
reports to the Vice President, Quality and Regulatory Affairs (VP, QS & RA)
and is responsible for supporting Quality Management System activities such as
supply chain, CAPA, application and analysis of testing and inspection procedures,
using metrology and statistical methods to diagnose and correct improper
quality control practices, understanding quality cost concepts and techniques,
developing and administering management information systems and auditing
quality systems for deficiency identification and correction. In
addition, this position is responsible for working with R&D on equipment
and process qualifications and validations.
Education/Experience
Required:
SC Quality Engineers must have a college
degree (Bachelor’s degree in a science field preferred) with a minimum of
5 years experience in quality engineering or management in a FDA regulated
industry with a thorough understanding of GMPs for medical devices, 21 CFR part
820, and ISO standards for medical devices and quality management
systems. Experience with drug GMPs, 21 CFR part 210/211, highly
desirable. Computer skills in MS Word, Excel and database programs
required. Experience with electronic document control systems is
desirable. Familiarity with and certification in Six Sigma, LEAN
manufacturing or other vigorous quality control programs is highly
desirable.
Physical/Mental Demands of Job:
This position is primarily office and
computer driven. However, the ability to work in a clean room environment
is an essential job function, as is the ability to communicate effectively
orally and in writing with the entire workforce. The ability to perceive
all aspects of the work environment, product and component samples and
documentation is essential. This position requires attention to detail,
excellent time and document management skills and the drive to complete and
follow-through for completeness. The ability to handle multiple
priorities in a fast changing work environment is essential, as is positive
interaction with others. Excellent problem solving skills and a team
approach to problem-solving and sharing responsibility is essential, as is the
ability to teach quality principals to others. Quality Engineers must be
able to work on multiple projects with a minimum of supervision and meet
established timelines. Strong interpersonal and communication (written
and oral) skills are essential. Job assignments are complex in nature and
require excellent planning, technical and communication skills to be successful
in meeting project objectives. Quality Engineers must be able to
coordinate and resolve both interpersonal and technical problems, including
conflicting “expert” opinions. Quality Engineers may be
required to travel to perform on-site evaluation of external suppliers' Quality
Management System or provide training and assistance to supplier personnel as
part of validation and qualification of suppliers' processes. Must be
able to maintain self-control in challenging circumstances and be reliable in
attendance and punctuality.
Apply with resume in word format to: Unilife.com
EEOC employer with competitive wages and
benefits.