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Production & Manufacturing / Quality
Ref No.: 18-17385
Location: North Palm Beach, Florida
Position Type:Right to Hire
Start Date: 03/15/2018
Hi, 

Good to know you are doing great ! 

PFA the below JD and let me know if you are open in the market along with the expected bill rate on W2. 
 

Production & Manufacturing / Quality
TCS - Boynton Beach,FL | North Palm Beach | North Palm Beach, FL
12 Months
ROLES & DESCRIPTION :
Ability  to work within a team environment and build relationships outside of the department as well as outside the company (suppliers, regulatory agencies, etc.).- Facilitates team efforts on quality engineering projects.- Ability to deliver, meet deadlines and have results orientation. - Adapts and is flexible and resilient in response to constraints, failures, and adversity.- Adjusts priorities to multiple demands and unanticipated events, and modifies decisions and actions in response to changing information and circumstances.- Able to communicate both orally and in written form to multiple levels of the company.- Microsoft Office Suite, expert knowledge of blueprint reading and geometric dimensioning and tolerancing, understanding of QSR/ISO regulations, design assurance, FMEA, and product testing methods, and are able to use optical comparators and CMMs.- Knowledge of statistics, process control, and process capability- Knowledge of the Quality System Regulation (21 CFR Part 820), the Medical Devices Directives (MDD) and other relations related to post market data.- Full working knowledge of all supporting department needs and capabilities, including the ability to discern when inaccurate information is supplied and offer ideas for how to correct it.
 
Process product complaints in a uniform and timely manner per established procedures.- Direct urgent issues to the proper personnel for report ability decisions.- Conduct complaint product testing and evaluation, if required.- Conduct and document accurate and thorough complaint investigations including review of DFMEA, P-FMEA and manufacturing documents where appropriate to ensure adequate identification, evaluation & investigation of an assignable root cause. Ensure quality issues are managed according to procedure and ensure adequate corrective/preventive actions are effective to eliminate/mitigate the issue.- Initiate CAPA Determination for complaints as applicable.- Support the rollout of any new CAPA solutions (tools, techniques, and/or process enhancements) in relation to the complaint investigation activities.- Review and approve Product Evaluation Reports and complaints for final closure as applicable.- Provide timely Health Hazard Evaluation (HHE) information from within the department and interdepartmentally, as needed to assist the HHE Coordinator.- Identify and implement improvements and innovations that increase efficiency and enhance work quality.- Participate in internal and external departmental audits and responses to cited issues.- Coordinate and work with extended teams to meet project goals.