Quality Engineering Team Lead
Location:
West Chester , Pennsylvania
Posted:
January 27, 2017
Reference:
4978161227-en-us

DePuy Synthes Companies is a member of Johnson & Johnson's Family of Companies, and is recruiting for a Quality Engineering Team Lead located in West Chester, PA.

 

DePuy Synthes Companies of Johnson & Johnson is the largest, most innovative and comprehensive orthopedic and neurological business in the world. DePuy Synthes Companies offer an unparalleled breadth and depth of products, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, craniomaxillofacial, power tools and biomaterials. Building on the legacy and strengths of two great companies, more agile and better equipped to meet the needs of today’s evolving health care environment. With a focus on activating insights to develop innovative, comprehensive solutions, we are inspired to advance patient care in greater ways than either company could accomplish on its own.


Position Overview

The Quality Engineering Leader devises or adapts new methods or procedures to control or coordinate all aspects of several projects simultaneously and in the solution of technical and related projects.  The Quality Engineering Leader is an emerging authority in a specific technical field, exercising considerable latitude in determining technical objectives of assignments.  Work is generally expected to result in the development of new or refined methods to reduce risk, equipment, materials, processes, products and or technical methods

The Quality Engineering Leader 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 and supervise, lead and mentor other engineers and technicians.

 

Major Responsibilities & Duties:

 

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, quality compliance, quality leadership talents 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 the development of quality strategies related to the transfer of products, materials and components within J&J or externally.  Supports new product introduction as part of design transfer.

 

People

• Provides supervision, mentoring, coaching, performance review, developmental plans, and succession planning for others (including Quality Engineers and Technicians)

 

Product Quality, Control & Disposition and Performance Standards

• Lead and maintain 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.

• Conduct stakeholder analysis to ensure that customer CTQs are known and adequately addressed in control plan

• Develop measurement systems/capabilities, destructive tests, non-destructive tests for manufacturing processes

• Develop control plans consistent with product classification, potential defect types, defect frequency, severity, patient risk, process capability, process controls, etc.

• 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.  

• Accountability and ownership for sampling plans of all types including acceptability of risk given the product classification, potential defect types, defect frequency, severity, patient risk, process capability, process controls, etc. including assessing, applying and interpreting acceptance sampling standard for manufacturing data.

• 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

• Conduct strategic planning with site leaders and Product Engineering Team.  Partnership with other functions to establish business priorities and resource allocation

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


Qualifications
• A minimum of a Bachelors Degree, preferably in Engineering or related technical field. 
• Requires 5-8 years related experience including 1-2 years supervisory experience.  
• 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 required 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 required.  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. 
• Strong mentoring, coaching and leadership skills are required. 
• Advanced knowledge and proven leadership in the areas listed in the Duties and Responsibilities associated with the position.
• Demonstrated project management and project leadership abilities are required.  
• This position may require up to 10% travel and will be based in a DePuy Synthes manufacturing facility.


Primary Location
United States-Pennsylvania-West Chester
Organization
Depuy Orthopaedics. Inc. (6029)
Job Function
Quality (Eng)

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