Set-Up Manufacturing Technician
Resume:
Lathrop, CA *****
Phone 209-***-****
E-mail ****.*********@*****.***
Antonio C. Panaligan
OBJECTIVE
EXPERIENCE
To establish a career in a progressive organization with opportunities for growth and improvement.
Revance Therapeutics Inc.,
Newark,CA Feb 2009 to present
Sr.Manufacturing Technician III
Prepared, set-up and ran fill process automation used to produce sterile pharmaceutical drug in class A clean room facility during media fills and clinical fills.
Responsible for supporting the equipment and personnel in the production utililizing aseptic and cGMP skills.
Performed, trained and suggested improvements for production process and equipment set-up, operation and maintenance.
Cross-supported engineering, validation, and research and development in executing protocols, to improve manufacturing processes.
Supported QC department in collecting water samples through facilities.
Assembly/disassembly of manufacturing equipment for product changeover procedures.
Hands-on experience in a GMP environment.
Sterilization using an autoclave and operation of a depyrogenation oven.
Prepare solutions based on specifications and written procedures
Document production by completing forms, logs, reports and records of equipment and batches.
Novo Nordisk, Hayward, CA May 2005 to May 2008
Process Technician
Performed aqueous-based drug compounding, sterile filtration, and aseptic form/fill/seal operations of small to large volumes.
Performed filling operations in a class 100/10,000 cleanroom facility and supports functions in a class 10,000 and 100,000 cleanroom environment both requiring appropriate gowning and qualification.
Performed parts preparation and autoclaving.
Performed equipment set-up, operation, adjustment, and shut down.
Performed batch record review.
Conducted training for manufacturing associates.
Supported equipment maintenance and calibration.
Worked with Engineers on continuous improvement projects.
Supported clinical manufacturing, development projects, and commercial scale-up.
Inamed Corporation, Fremont, CA Nov. 2003 to May 2005
CR Manufacturing Technician II
Maintained of an aseptic environment by sanitizing equipment and clean room surfaces and preparing samples for QC testing.
Cleaned, assembled, wrapped and autoclaved equipment and materials as needed for the clean room operations.
Assembled, inspected and tested integrity of equipment and filters per schedule.
Acquired qualification in aseptic gowning procedures as required.
Maintained weekly personal monitoring counts within acceptable levels.
Prepared and steriled filter product buffers and solutions, including weighing and measuring materials and pH solutions.
Aradigm Corporation, Hayward, CA July 2000 to July 2003
ManufacturingTech II
Setup the FFSO1 at a moment notice to run as required by the validation staff.
Assisted engineers to set up and operate the FFSO1 as required. Troubleshoot the programming of the FFSO1 HMI and PLC.
Assisted in the development of training materials and performed ongoing training and implementation of changes to procedures.
Assisted Validation Engineers in the creation and execution of validation protocols.
Held aseptic training session for operators to ensure proper aseptic technique when performing activities specifically on the FFSO1.
Performed routine Preventive Maintenance Standard Operating Procedures while operating in a manner compliant with GMP’s.
Trained co-workers, which resulted in, increase productivity and reduction in lead-time.
Mcghan Medical Corporation, Fremont, CA Feb 1993 to July 2000
Manufacturing Technician II
Prepared equipment and materials for use in the clean room.
Prepared buffers and solutions and sterile filtration.
Performed integrity tests on equipment and materials.
Set up equipment for CIP/SIP operations.
Set up fill-lines and automated filling equipment.
Assembled automated batch processing equipment aseptically.
Performed batch filtration, precipitation, screening, bottle filling, centrifugation, homogenization, and unit product filling.
Trained fellow employees on manufacturing processes.
Cygnus Therapeutic Systems,
Redwood City, CA Sep. 1991 to Jan. 1993
Production Coordinator
Manufactured clinical materials according to GMP guidelines. Under some direct and some indirect supervision, performed the operations necessary to make supplies for test in clinical studies. Communicated production status, suggestions for improvements and problems.
Completed inventory control and dispensing activities for GMP raw materials.
Collected, maintained and interpreted data on operations performed.
Revised, updated and/or developed new processing records and
Assisted machine operator CP11 clockner.
Performed line clearance.
Supervised and led all activities on the swing shift department.
Coordinated operations with teamwork among machine operators and line attendant.
EDUCATION
Immaculate Conception Academy High School (1982)
Computer Learning Center, Manteca Ca (1999)
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