Medical Device Manufacturing
Resume:
[pic]Joseph Azarcon
Sunnyvale, CA 94089 ? Cell: 408-***-****
? *************@*****.***
Profile
Production Supervisor, Production Lead, Production Operator of
Product Development and Production of product with more than 10
years of experience in Medical Device Company that develops new
products for patient care and medical device.
Professional
Experience
CareIndeed Agency, Part Time Caregiver
Dec. 2013 to Present
Menlo Park, CA 94025
. Assisted in bathe and maintained personal cleanliness
. Encouraged activities in line with the client's needs and
capabilities
. Washed and dried clothes of client
. Helped toileting and incontinence care
. Documented client's care in suitable forms
. Reported unexpected changes of the client's physical, mental
or emotional health to the family and agency
. Made the client's bed and changed the bed sheets
Manufacturing Supervisor, Duke Empirical Medical Device Company
Santa Cruz, CA 95059
Aug. 2012 to Dec. 2012
+ Job entailed all the manufacturing supervisory duties
described below in the Sub-Assembly Catheter manufacturing
position. Additional duties included regular meetings with
Operators, Management Teams and Quality Management. Performance
reviews of all operators were conducted as required. Responsible
in maintaining Safe, Quality, Team, Housekeeping and Healthy
Environment.
. Provides technical support relating to equipment utilized in
the manufacturing areas by repairing, maintaining, or modifying
production equipment utilizing technical expertise, technical
manuals, schematic drawings, precision tools, and test
equipment.
. Responds to assembly line equipment repair calls, by
diagnosing equipment problems, and performing the necessary
repair.
. Documents equipment qualifications and upgrades made to
existing machines, including preventative maintenance performed
and parts used, to ensure appropriate documentation of repair
history in the MP2 maintenance database.
. Supporting production line in Equipment Preventive
Maintenance, Equipment Calibration, Change Order, Opening and
closing Corrective Action Preventive Action (CAPA) and NCMR.
Manufacturing Supervisor, Boston Scientific, Fremont, CA 94538
Jan 2008 to Nov. 2008
Accepted the position as Temporary through TACWORLD Agency.
Production of Stent sub-assembly and Stent Delivery System,
Production of Grinding and Coating Guide wires and Extrusion
Production Line.
+ Communicates with Management Team, Maintenance Team, IS Team,
Calibration Team, Quality Group, Industrial and Manufacturing
Engineers.
+ Supporting Manufacturing Engineer and Quality Engineers for
Change Request, Deviations, Identifying Non-Conforming
Materials, Issuing and Closing NCR form
+ Organized meetings with the Team / Management.
+ Ensures Safety pre-cautions are being followed to maintain
safe work practices and 0% accidents.
+ Maintaining quality of work of all Product Builders and Daily
production goal.
+ Schedule, Train, Motivate Product Builders.
+ Supporting IE in implementing LEAN Manufacturing and making
sure all Product Builders are following LEAN, Process
Instructions and Line Clearance Procedure.
+ Reporting and Updating CORE 5 MATRIXES for Daily, Weekly and
Monthly Report
+ Scheduling Committed Build Plan on the production floor.
+ Opening, Reviewing and Closing Shop Floor Paper Works.
+ Monitored Attendance, Lunches and Break Time. Scheduling
Vacations/Timecards and Training Records are up to date.
+ Reward and recognize accomplishments of Product Builders.
Manufacturing Supervisor, Abbott Laboratories, Santa Clara, CA
Formerly Guidant Corporations.
+ Drug Eluting Stent (DES) Pilot Line Manufacturing -
Transferred to DES Pilot Line when Guidant's Stent Production
was moved to Temecula, CA. Work as a Production Lead for 7 years
then promoted to Manufacturing Supervisor and held the position
for more than two years until Abbott (formerly Guidant downsized
the operation in December 2007, this position was eliminated.
+ Job entailed all the manufacturing supervisory duties
described below in the Stent and Catheter manufacturing
position. Additional duties included regular meetings with
operators, management teams and Quality Engineers. Performance
reviews of all operators were conducted as required. Responsible
in maintaining Safe, Quality, Team, Housekeeping and Healthy
Environment.
Production Lead, Guidant Laboratories, Santa Clara, CA 95051
1998-2001
Stents and Catheters - Production of ACS Multi-Link, Megalink,
Ultra, Herculink, Solo, Acculink and Dynalink Stents and
Catheters.
+ Initial assignments as Assembler for a few months involved:
Laser Machine Operator, Wet Chemical processing - descaling,
Cleaning and Passivation. Manual and Instrumental (ROI)
measurements of Stent's dimension.
+ Quickly promoted to Production Lead facilitating and
coordinating production activities of 25 to 50 Operators.
+ Responsible for: Opening, Reviewing and Closing Lot History
Records (LHR), Inventory of production materials and supply.
+ Gathering components for assembly, Training and assigning
stations to operators. Monitored Training Records.
+ Obtaining necessary approval prior to and after completion of
work.
+ Ensuring the quality of all operations by making sure that the
Operators follow the Manufacturing Process Instructions.
+ Ensures Safety pre-cautions are being followed to maintain
safety work practices.
+ Updating hourly board for production yields, Collecting and
summarizing data for daily, Weekly and Monthly reports,
+ Laser set-up and adjustment, Ensuring equipment are well
maintained and in proper working condition,
+ Assisting Manufacturing Engineer in prototype works and
Quality Engineers for quality improvements.
Other Employment: ELECTRONIC MANUFACTURING INDUSTRY - Two
Years
Document Scanning Clerk - ATI Advanced Imaging, Milpitas, CA
Oct. 2004 to Nov. 2004
Production Expeditor - National Semi-Conductor, Santa Clara, CA
July 1997 to Nov. 1997
Line Operator/Test Technician - Quantum, Milpitas, CA
Feb. 1997 to May 1997
Test technician/Assembler - SAE, Santa Clara, CA
Oct. 1996 to April 1997
Assistant Lead - Acer Computer Company, San Jose, CA
Sept. 1995 to Dec. 1996
Highlights:
+ At ATI Advanced Imaging, Part-time secondary employment
through VOLT Agency - Film Scanning and Visual verification of
digital image quality. Data Entry and Machine operator.
+ At National Semi-conductor, Wafer fabrication. Responsible for
scheduling and inventory of daily runs. Prepared documentation
to start and close production runs.
+ At Quantum, Performed pre and final inspection of disk drives;
configured hardware according to customer specifications.
+ At SAE, Part-time job. Performed final test for different
kinds of circuit boards and cables. Responsible for daily
reports for assembly and test areas.
+ At Acer Computer company, Started as Computer assembler,
progressed to pre-release testing of assembled computers. During
the last 8 months of the assignments', work as Lead -responsible
for daily reporting of finished goods shipped to the warehouse,
inventory of packaging materials, summary of all "burn-in"
tester, final test report and data entry for production
statistics. Assisted Supervisor in contacting vendors for
packaging materials.
Education/Training
?High School Graduate and some Colleges in the Philippines
?Good Manufacturing Practices
?Lean Manufacturing Tool Guide
?5CORE Matrix
?Supervisory Skills and Managing People
?Safety and Chemical Hazardous Training. ERT Training.
?Training sponsored and provided by current and previous
employer.
Qualities/Personal
?Interpersonal and Organizational Skills, Good with people and
numbers. Hard Worker, Stable, Reliable, Flexible and Quick
Learner. Attentive to details. Follow through on assignments and
completes task on time. Proficient in EXCEL, WORD, GRAPHING,
POWER POINT, SAP System and PDM.
?US Citizen, Excellent Health. Interest in Gardening.
Contact this candidate