From: route@monster.com
Sent: Wednesday, August 10, 2016 8:30 AM
To: hg@apeironinc.com
Subject: Please review this candidate for: Safety Coordinator
This resume has been forwarded to
you at the request of Monster User xapeix03
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Anh-Tuan Leduc 1200 S. Marin Ct Anaheim, CA 92804 Cell (714) 728-2536 anhtuanleduc@gmail.com Objective:Seeking
a challenging position in Manufacturing Management with an opportunity for
growth and career advancement from within the organization. Qualified
by: ·
Experienced Production Supervisor with over 20 years in a
medical product manufacturing environment. ·
Completely familiar with cGMP’s, FDA Quality System
Regulations, ISO 9001, ISO 14001, Cal OSHA. Business
Experience: Aug
2007 toST JUDE MEDICAL, Irvine, CA
– medical device manufacturer PresentProduction
Supervisor ·
Responsible for the manufacturing activities and personnel
involved in the manufacturing of catheters. ·
Schedule staff and production activities focused on
meeting customer demand. ·
Plan and execute daily/weekly schedules, ensuring
inventory appropriateness, and application of correct capacity through
cross-training of associates. ·
Train, mentor/coach new employees, monitor employee
performance, writes and delivers employee performance reviews. ·
Responsible for soliciting and communicating potential
improvements in processes that may reduce cost, increase quality, and/or
improve delivery of products through continuous improvement, lean
manufacturing principles ·
Provide training and coaching to improve standard work,
work center organization (5S), and housekeeping. ·
Lead two Value Stream Teams. ·
A member of EHS team. ·
Ensure employees adhere to Company policies and
procedures, safety rules, and employee code of conduct. Administer corrective
actions as necessary. ·
Ensure adherence to all ISO and FDA regulations. ·
A key person in production
supporting the FDA,BSI and TUV audits. ·
Interact with R&D, ME and QA engineers to ensure
smooth transactions of all new products release to production. March
2001 toMICRO GAGE, El Monte, CA – semiconductor
manufacturer Aug
2007Production Supervisor ·
Direct and coordinate the activities of employees engaged
in the production of Sensor and Transducer departments to meet sales, quality
and cost requirements. ·
Assist Engineering personnel in developing new products
and improvements to manufacturing methods. ·
Plan and schedule production operations to produce
products in a timely manner while maintaining an efficient flow of work to
obtain maximum utilization of material, manpower and machinery. ·
Provide guidance and direction to subordinates, include
setting performance standards and monitoring subordinates. ·
Oversee the safety programs including monthly safety
meeting, employee safety training, and conduct accident investigation
with proposing corrective actions. Nov
1993 toMEDTRONIC PERFUSION SYSTEMS,
Anaheim, CA – leading medical device manufacturer Sept
2000Production Supervisor – 1st,
2nd and weekend shift ·
Responsible for administering and supervising the
manufacturing activities and personnel involved in the manufacturing of
Custom Tubing Packs product for open-heart surgery. ·
Managed and supervised 1 supervisor, 3 data entries, 1
trainer, 15 assembly team leaders, 8 warehouse persons and 120 assembly
technicians. ·
Responsible for the employment training, safety,
employment motivation and discipline of employees supervised. ·
Developed assembly technicians into strong team leaders
and implemented self-managed teams Anh-Tuan Leduc
·
Coordinated and expedited flow of materials, parts, and
sub-assemblies between departments according to production/shipping schedules
and department priorities. ·
Member of inter-department team that installed “BPCS”
business software running on AS400 computer. March
1990 to ADVANCED
INTERVENTIONAL SYSTEMS, Irvine, CA – leading Laser catheters manufacturer Nov
1993 Production Supervisor- 1st
and 2nd shift ·
Responsible for employees involved in the processing of
fiber optic catheters used in angioplasty surgery. ·
Developed plans to accomplish work, prioritized and
organized the work force to meet department goals. ·
Responsible for the efficient operation of clean room
activities to support production build plans to comply with FDA regulations. ·
Supervised 4 team leaders and 42 assemblers. ·
Maintained operations data, such as time, production, and
cost records and prepared management reports. ·
Maintained safe working conditions and provided training
to personnel on proper handling of chemicals involving in the
production floor. May 1988 toMEDTRONIC PERFUSION SYSTEMS, Anaheim,
CA- leading medical device manufacturer
March 1990Production Supervisor
·
Responsible for the
activities of 37 employees engaged in producing of critical cardiovascular
products (Blood Filters, Cardiotomy Reservoirs, Venous Reservoir Bags and
Hollow fiber Oxygenators) ·
Planned and established work schedules, assignments to
meet production goals. ·
Maintained an adequately skill work force consistent with
planning requirements. ·
Provided information to and collaborated with Engineering,
Quality Assurance and maintenance to effect
cost reduction, work simplification. Education: Cal State Fullerton, Fullerton, CA Major: Computer Science Santa Ana College, Santa Ana, CA Major: Business Information Science Seminars
and classes attended: ·
US-FDA Quality System Regulation ·
Customer focus quality programs ·
Quality leadership process ·
Productivity through automation ·
Education in quality improvement projects and techniques
(6 month class) ·
Leadership to total quality management ·
Productivity improvement through employee ·
Team development ·
Facilitating for results ·
Train the trainer ·
Assertiveness training ·
Sexual harassment prevention ·
Managing Conflict Effectively Board
of Pharmacy license: ·
Manufacturer of dangerous drugs |
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