Quality Manager Resume
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SUMMARY
- Professional with experience in fast - paced environments demanding strong technical, organizational and interpersonal skills. Hands on driven professional focused in achieving goals through process effectiveness.
WORK EXPERIENCE
Confidential
Quality Manager
Responsibilities:
- Quality assurance of product and service.
- Quality assurance of product through GMP and ISO Guidelines and respective continuous education. Organize periodical internal audits to challenge existing status. Responsible for external audits from pharmaceutical customers. Establishing quality requirements for suppliers.
- Quality assurance of service through process improvement, producing quality products: follow trends and findings for production process improvements and defects prevention.
Confidential
Senior Manufacturing Engineer - Process Improvement Lead
Responsibilities:
- Project coordinator of all process improvement initiatives using lean and six sigma tools.
- Lean Manufacturing Trainer and Lead for the Puerto Rico Operations. Creator of Lean Manufacturing Program and implementation.
- Creator of Standard Work procedures, visual aid and training. Creator of 5S procedure, buyer’s standard and audit form.
- Development and creation of the Plants Metric System. Implementation of Real Time Electronic Metric System. Software development advisor.
- Leader of facilities changes and layouts to implement continuous visual flow. Assuring all cells comply with lean principles and initiatives. Assure design of new clean room also complies with lean initiatives.
Confidential
Lean Manufacturing Trainer and Lead
Responsibilities:
- Coordinate and support all new product integration and product transfers by assuring their manufacturing processes are designed under the lean manufacturing principles. Leader of 3P Events. Responsible for the integration of new equipment for the plant. Coordinating resources for the installation, validation and process integration.
- Lead Facilities Department at all facilities changes that come along new manufacturing cell from new products or transfers as well as for Kaizen Events.
- Responsible of implementing the Lean Principles and decrease the amount of wastes to maximize plant productivity at all levels.
- Perform Kaizen events and lean tools in order to improve on time delivery to 97% and decrease inventory by 50%, along with process cycle time and lead time 35% reduction on various aerospace electromagnetic assemblies production lines.
Confidential, Arecibo, P.R.
Manufacturing Supervisor
Responsibilities:
- Lean Manufacturing Awareness Trainer.
- Leader of five production lines and a minimum of forty five employees.
- Leader of Departmental Team responsible of answering Customer Complaints, Non Conformances, generating problem solutions, product integration and certification, and monitoring Quality Inspection Program. Ensure all Lean principles are being followed.
Confidential, Arecibo, P.R.
Molding Process Engineer
Responsibilities:
- Integration manufacturing of parts in outside suppliers to be manufactured in house. Cost estimates for new integration of parts. Applied Statistical Process Control to report on process performance, quality level and compliance using defect data on Pareto charts, scrap and % yield reports.
- Support for the Bulk Molding Compund Mixing Department. Creation of new layout and ergonomics evaluation. Created a new identification label for the BMC material providing expiration dates, batch number and description important for FIFO, best used dates, and other key process indicators.
- Creation of the Manufacturing Instruction Letters which was used as PM, Visual Aid and Quality Criteria for all molding areas (BMC compression molding, SMC and BMC injection molding and thermoplastic injection molding).
- New molding facility layout - directed the reorganization in compliance with the layout design of the 50 machines that compose the molding area.
TECHNICAL SKILLS
- Fully fluent in Spanish and English
- Licenses And Certificates
- Lean Manufacturing Certification, University of Michigan 2006
- Six Sigma Certified
- FDA Quality System Regulations Certification
- CAPA Certified
- Computer Skills
- Proficient in Microsoft Office, including Project and Visio applications; CAD Layouts/drawings, Professional Presentations, Minitab, SPSS
