Quality Technical Leader - Medical Device

We are looking for a Quality Technical Leader - Medial Device for a 3 months contract position in Roswell, GA.

RESPONSIBILITIES:

1) Development of the Risk Management files which includes Product Hazard list, Design FMEA, Use FMEA & Process FMEA. 
2) Development of Quality Function Deployment documentation. 
3) Ensure that all elements of the corporate Human Resources Development and Diversity policy are fully supported as appropriate for the position. 
4) Manage self and/or team in accordance with the expected behaviors of the Leadership Qualities. 
5) Provides technical leadership in solving more challenging technical problems related to quality issues and technologies. 
6) Develops, initiates, and implements new quality concepts, tools and strategies to improve business practices. 
7) Solves highly technical complex problems, provides expertise in related specific field of knowledge and consults on complex issues and projects. 
8) Assists with the transfer of knowledge of technical skills and is viewed as a Subject Matter Expert. 

ENGINEERING AND LEADERSHIP FOR MEDICAL DEVICE NEW PRODUCT DEVELOPMENT (90% OF TIME) 
Actively participate in and/or facilitate the development of deliverables required for medical device product development. 
Actively participate in the development of product development plans, specifically components that focus on design reviews, quality plans, design transfer, and design verification/validation. 
Direct all activities necessary for the project team to achieve design control deliverables, specifically deliverables related to product safety and performance. 
Ensure new products meet customer requirements and specifications. 
Lead and ensure compliance to all risk management requirements. 
Partner within cross functional teams to determine root cause and mitigations of product issues as they arise during development. 
Where appropriate, implement Design of Experiments and Problem Analysis/Solving concepts in conjunction with R&E. 
Actively participate in the development of statistical plans and rationale for design control activities/requirements. 
Actively partner with the project teams to facilitate the incorporation of all quality system elements, root cause analysis, corrective action and continuous improvement principles throughout the entire product redesign. 
Support and facilitate updates to the Design History File. 
Where appropriate, incorporate the concepts of Lean Six Sigma to solve product/process nonconformance issues. 

Deliverables, Responsible for Developing: 
Risk Management files 
Quality Functional Deployment for Design Transfer 
Validation Acceptance Criteria 
Release of Investigational Product for Clinical Evaluations 
Design History File 
Initial Release and Revisions to Design/Input Forms 
New Supplier Qualifications 

DELIVERABLES, REVIEW AND APPROVAL: 
Design Reviews Plans 
All Design Verification and Validation Protocols and Reports 
All Design Verification Testing Specifications 
All Process Validation Protocol and Reports (IQ, OQ, and PQ) 
Regulatory Strategy Plan 
Manufacturing Strategy Plan 
Device History Records 
Design Transfer Plan 
Supplier Approval Plan 
Annual Post Market Review 

Systems Compliance (10% of time) 
Ensure new product development is in compliance with medical device regulations and internal procedures. 
Implement the Root Cause Analysis concepts to investigate issues requiring Corrective and Preventative Actions. 
Lead, participate in and/or facilitate in monthly complaint review meetings (as needed). 
Review, approve and be actively involved in the maintenance and updates to design history and risk management files. 
Participate in internal and external audits as needed. 
Maintain personal compliance to all internal systems as required, such as training.

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