Quality Engineer II
Location:
Cornelia , Georgia
Posted:
April 02, 2017
Reference:
5589170321-en-us

Ethicon, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a Quality Engineer II, located in Cornelia, GA.
 
Ethicon, Inc. is a trusted, world-wide leader in surgical care. For over a century, Ethicon has continuously introduced innovations in wound closure, general surgery, wound management, women's health and urology and aesthetic medicine that fulfill the company's vision: Restoration of Body and of Life.

The Quality Engineer conducts assignments encompassing complete projects or portions of major projects.  They determine methods and techniques to be used or adapt standard methods to meet variations.  They coordinate phases of work internally and externally.

The Quality Engineer will utilize Quality Engineering tools and practices for the effective and efficient development, transfer and maintenance of products/processes throughout the product lifecycle. The incumbent will also utilize Quality Engineering principles and problem solving skills to improve and maintain products/processes that are aligned with the overall Quality and Business vision. He/she will utilize appropriate risk management to prevent unanticipated failure modes and improve capability of processes.  This person will support processes in base business.

Business Improvements
Support quality improvement initiatives such as process and product characterizations that lead to continuous / cost improvements.
Review/analyze the effectiveness of PDCA, Six Sigma, Kaizen, Lean Techniques and/or other improvement tools and programs.
Conduct benchmarking to develop more effective methods for improving quality
Supports the development of quality engineering and quality compliance with the right skill sets for new product introductions, and product life cycle management. 

Compliance/Regulatory
Review/analyze whether current product and processes (including actions or decisions conducted) are in compliance to standards such as the QSRs, ISO 13485, etc.
Champions compliance to applicable Global Regulations and standards (e.g. QSRs, ISO, EN and Medical Device Directive (MDD) requirements) including providing support during internal and external audits.
Conduct periodic line audits to assess for production controls such as lot segregation.  Review results of area audits to ensure that corrective and preventive actions are adequate.

New Product/Process Introduction
Partners with R&D and other cross functional partners to ensure the proper application of design controls, risk management and the investigation/correction of design failures/challenges.  
Supports new product introduction as part of design transfer.

Product Quality, Control & Disposition and Performance Standards
Supports activities related to the Material Review Board.  
Conduct investigation, bounding, documentation, review and approval of non-conformances, CAPAs and customer complaints.  Escalation of quality issues as appropriate.
Accountability and ownership for material identification, material segregation, classification of defect types including the successful application of these techniques on a day-to-day basis in manufacturing.  
Analyze/review effectiveness of preventive and corrective actions.  Review root cause investigation according to an established process.
Accountability and ownership of Quality metrics including maintenance and reviewing of leading and lagging indicators of quality

Product/Process Qualification
Approve IQ, OQ, PQ, TMV or Software Validation

Production/Process Controls including Control Plans
Partners with J&J Global Supply chain, Finished Goods and material suppliers to ensure appropriate application of process validation, process control, and risk management; and the investigation/correction of process failures when needed.
Develop, interpret and implement appropriate process monitoring and control methods consistent with the level of process/product risk. 
Collect data and execute/conduct various analytical/statistical analysis and interpretation as part of process improvements and day-to-day support.  
Develop, interpret and implement standard and non-standard sampling plans
Assess effectiveness of measurement tools, destructive tests, non-destructive tests, measurement system analysis.  
Assess and interpret common versus special cause variation in manufacturing processing and determine adequacy of current process limits.

Risk Mitigation
Document, justify, review or analyze whether a proposed change to a process will not enhance the risk level in some way beyond capability of current controls or whether change will result in potential non-compliance to a required standard such as the QSRs
Assess the need for risk mitigation techniques given product classification, potential defect types, defect frequency, severity, patient risk, process capability, process controls, etc. Determine effectiveness of these techniques on previously implemented improvements

Strategic
Ensures effective quality strategies are created for the validation of test methods, process and design.   

Qualifications
A minimum of a Bachelor’s Degree, preferably in Engineering or related technical field.
A minimum of 2-4 years related experience is required.  
Experience working in both an FDA and European regulatory environment is preferred. 
This position will require relevant experience working in manufacturing/operations.  
In-depth knowledge of product/process Risk Management (FDA and ISO standards) is required.
Experience with a proven track record of implementing appropriate risk mitigation. 
Technical training and experience using Statistics, Lean and Six Sigma Methodologies is preferred including Measurement System Analysis, SPC, DOEs, Reliability, etc.  
Strong knowledge of statistical software packages is preferred with the ability to preview, graph and analyze data and be able to present data that facilitates/drives decision making. 
The ability to perform "hands on" troubleshooting and problem solving is preferred.  The ability to think on the feet and providing sound judgment is highly desired. 
Good technical understanding of manufacturing equipment and processes is required. 
Understanding of the NPI (New Product Introduction) process and Process Validation expertise is preferred. 
A thorough understanding of GMP/ISO regulations and validation regulations is preferred. 
Demonstrated project management and project leadership abilities are preferred.  

BE VITAL in your career, Be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies.

J2W: LI NA

Primary Location
United States-Georgia-Cornelia
Organization
Ethicon Inc. (6045)
Job Function
Quality (Eng)
Requisition ID
5589170321

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