Raymond M. Empleo

**** ****** *** ***** **** CA *0620

714-***-****

Objective

Looking for challenging work environment that enhance my professional skills & experiences.

Have over 13 years experience in Manufacturing Technician in Pharmaceutical industry.

Knowledge of wide range material and processes. Committed to quality and safety, able to

delegate and solving complex problem.

Skills:

Knowledge of SOP, GMP, Microsoft Word, Excel.

Experience

Kerr Corporation/Scientific Resources 05/24/07 12/06/13

QA/QC Senior Lead Inspector

Supervise and coordinate activities to Quality Inspectors in testing and inspection and scheduling

to ensure the product release on time.

Makes Certificate of Analysis per customer request.

Performed incoming closed tolerance Dental precision parts; such as Syringes, Cartridge, Mixing

tips, Curing light, Tools and Labels.

Received raw materials from vendor and performed testing to make sure passes the particulate

limit. Generate non conformance if needed.

Performed visual and dimension inspection, verified against Master Control to ensure 100%

compliance and verified Certificate of Analysis. Generate nonconformance as needed.

Performed first article in filling and packaging department, inspect and verify correct and legible

information are printed on the carton and tray lot number referencing ANSI ASQC Z1.4.

Verified label artwork, lot number, and bar code for the correct product name.

Calculate and record mathematical data onto proper form and report unusual observation to

supervisor. Initiate nonconformance as needed.

Performed in process testing of Dental product according to Manufacturing Instruction; calculate

result and complete all appropriate document and release per procedure.

Reviewed the accuracy of Work Order and verified component for intolerable defects including

product mix up, and generate Nonconformance in accordance with Standard Operating

Procedure (SOP).

Reviewed Work Order to ensure compliance per procedure and file.

Attained perfect attendance for seven consecutive years.

Vita Tech International 02/19/07 05/04/07

QA/QC Inspector

Performed line clearance in packaging line and verified the correct and legible information printed

in the box matches information against Work Order.

Reviewed and verified Work Order to ensure compliance per procedure.

Inspects, testing and released raw material per procedure.

Performed in process testing; such as compression testing, tablet weight, hardness, thickness,

friability, and appearance, and release in accordance with Standard Operating Procedure (SOP).

Generate nonconformance report as needed.

Pacific Rim/Bio Rad 03/23/06 12/01/06

QA Inspector

Performed first article in packaging and filling line to ensure proper set up has taken placed to

package on designated Tiromat or carton line.

Randomly inspect vials (reference to the ANSI ASQC Z1.4 1993 sampling method in QA

Compliance) for defect that include: incorrect label information, expiration date, missing labels,

low fill volume of product solution.

Reviewed the accuracy of Work Order and verified appropriate component, calculate and record

mathematical data onto proper form and report unusual observation to supervisor.

Initiate nonconformance as needed.

Corda Enterprises 06/15/03 03/20/06

QA Inspector

Perform in process inspection.

Inspects, product packaging for accurate torque of lid and weight requirement.

Verified labels and inkjet codes matches the product specification and are placed properly.

Received product from vendor and verified the accuracy of paperwork to ensure quality system

requirements.

Reviewed and compile paperwork to ensure compliance and released product per procedure.

Responded to inbound/outbound sales calls, quoting and marketing product

Alpha Therapeutic 04/15//02 06/10/03

Manufacturing Technician III

Cleaned and set up equipment for production. Processed Immune Globulin Intravenous (IGIV)

human suspension and filtration.

Tested, monitored, scheduled and produced plasma bi product.

Eliminate downtime and improved productivity by efficiently maintaining equipment and replacing

worn parts before breaking.

Made suggestion to management, which improve safety and production process.

Handled records of GMP, SOP, and MI Training.

Baxter Bioscience 03/09/97 10/10/01

Manufacturing Technician III

Monitored controlled product weight, volume, temperatures, and ph adjustments.

Processed suspension B @ 17% filtration.

Handled records of GMP, SOP and MI training.

Selected to train newly hired employee of all policies and procedures to be independently productive

within a month.

Achieve error free result for twelve continuous month (no deviation report) by focusing key activities

adhering to Standard Operating Procedure (SOP).

Perfect attendance for full year.

Premiere Cruise Ship 05/31/94 02/31/97

Boiler Operator

Maintaining compressor and air dryer to meet the demand of entire ship.

Inspects, maintained and maid mechanical repairs on all types of equipment in the boiler and engine

rooms in timely manner.

Made adjustment to chemical treatment and chemical mixtures to establish desired values for ph; such

as chloride, sulfite, phosphate hydrate and total dissolved solids.

Performed preventive maintenance on all type machinery associated with the production of high

pressure steam and chilled water to heat and cool in entire ship, thus minimizing equipment downtime.

Certification/Licenses

License in Steam Plant Operation, 500 HP, 2000

Los Angeles Technical Institute of Los Angeles CA

A.A., Marine Engineering, Technological Institute of the Philippines

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