JT682 - ASSOC PROCESS IMPROVEMENT ANALYST
Summary
Analyzes and optimizes manufacturing processes (Lean/Six Sigma) in pharmaceutical/biotech/medical devices, focusing on waste reduction, line balancing, and performance metrics to drive continuous improvement in Puerto Rico/USA facilities.
Responsibilities:
- Plans, performs and implements process improvement initiatives (such as Lean or Six Sigma).
- Diagrams and evaluates existing processes.
- Organizes, leads and facilitates cross functional project teams.
- Develops metrics that provide data for process measurement, identifying indicators for future improvement opportunities.
- Collects data to identify root cause of problems.
- Measures performance against process requirements.
- Aligns improvement to performance shortfalls.
- Provides consultation on the use of reengineering techniques to improve process performance and product quality.
- May deliver presentations and training courses including measurement, analysis, improvement and control.
- Surveys and analyzes best practices for techniques and processes.
- Managing daily tier management systems, applying lean manufacturing techniques to eliminate waste, optimizing both material and information flow, and driving continuous improvement initiatives while considering appropriate ergonomic controls in clean rooms and non-clean room manufacturing areas.
Qualifications:
- Bachelor's degree in Industrial Engineering Required.
- 2 plus years of relevant experience
- Experience and/or knowledge in conducting time studies and production line balancing, preferably with knowledge of Lean Manufacturing and/or Flow Acceleration.
- Working Shift: 1st shift
Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.