Medical Device Manufacturing Company seeks Quality Manager. Candidate would be responsible for managing and controlling Quality Management system to meet ISO 9000 and FDA requirements. Manage documentation records for compliance as required for retention, MRB process for nonconformance, liason on regulatory issues (UL, 510K, ROHS), DHR reviews, CAPA, GMP compliance, Supervise 5 technicians. Bachelor's degree in related field, Seven years experience in various Manufacturing quality system. Medical ...
My name is David and I represent The Fountain Group. We are a national staffing firm and are currently seeking a Quality Engineer for a prominent client of ours. This position is located in Jacksonville, FL Details for the positions are as follows:
Initiate and monitor supplier investigations, non-conformances and CAPAs (60%)
Initiate and monitor supplier changes (10%)
Supports the supplier add/change process for the Approved Supplier List. (10%)
~~Requisition # : 44684
Date Submitted : 8/7/2014 8:16:04 AM Positions : 1
Start Date : 9/1/2014 End Date : 9/1/2015
Order Status : Open Order Type : Requisition for Contract Labor
Required Travel : U. S. Domestic Travel Required
Work Environment : Professional Anticipated Schedule : Typical 8 Hour/Day
Contractor Work Location : 6743 Southpoint Drive North Jacksonville, FL USA
Labor Category : Engineering
Job Family : ...
1 Year Contract
Completes Design History File documentation
Creates and delivers presentations throughout the organization,
Design of Experiments (DOE) and Statistical Process Control (SPC),
Determines manufacturing operation requirements and process parameters
Develops plans to evaluate process repeatability and stability
Develops product and process improvements
Participates in internal supplier audits
Performs process and equipment validations
Provides technical ...
Location: Jacksonville, FL
Validation Lead II
I. Write a brief summary statement of the basic purpose(s) of this position, i.e., why the position exists and its purpose in the organization.
Manage the development & implementation of software validation policies and procedures. Manage/conduct software validation projects in support of existing computerized systems in the Jacksonville campus. Project responsibilities will be focused on medium to large validation projects. This position may also ...
ALL COMMUNICATION IS STRICTLY CONFIDENTIAL
A progressive, well-established, full service, state of the art, forty man production laboratory is looking for a Fixed QC & Technical/Clinical Supervisor to relocate to Bartlett, TN.
We would prefer a candidate who has experience in a similar position as well as employment history in a reputable production lab.
Most important the person needs to be very comfortable talking with dentists on technical/clinical matters, to include treatment planning of ...
The IT Quality Manager is responsible for developing and overseeing the quality management system and quality assurance function to ensure IT projects & activities meet the quality goals of the organization. The Manager – Quality leads the development and establishment of the Quality Management System (QMS) comprising project methodology & standards and provides on-going support to the project teams.
Bachelor’s Degree in Information Technology, Computer Science, or any other ...
Payspan, Inc is seeking a strong QA Analyst, performing a large range of duties related to the origination and servicing of indirect/direct retail installment sales contracts.
The QA Analyst works in full life cycle quality assurance. Prefer candidates with SQL experience
Responsibilities include the Essential Functions:
Responsible for Quality Reviews, requirements and identification of significant trends.
Executive of Quality Test Plans, using established formats and templates.
Remedy has an exciting new opportunity located in Flemming Island.
We are looking for an candidate that has experience with quality and management.
-Attention to detail
-Ability to multitask
If you have knowledge of AS9100, Aerospace and FAA this is a plus.
Must be flexible and able to work overtime.
Salary will be between $40,000 and $50,000 starting out.
If interested please submit your resume for review.
The Quality Control Coordinator proactively creates and manages departmental metrics that impact cost and coordinates functions associated with quality control and environmental processes and procedures. The position involves creating and providing quality checklists to ensure standards are met in our packaging/distribution divisions.
Ensures department meets quality goals on a daily basis.
Identifies, documents and shares departmental ...
Quality Control/Sales Assistant
Job Description: Inspect product from start to finish making sure product meets all requirements and standards in the boat building process. Ensure that the quality standards are met by every component of the product or service provided by the company.
Quality Control Job Duties include but are not limited to:
Monitor the development of all products manufactured by the company.
Monitors every process involved in the production of product manufactured.
Ensure the ...
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