Process Technician

Anthony Ruben Lewis

**** ********* **. # ***

Grand Prairie TX, 75050

817-***-**** (Home)

817-***-**** (Cell)

Objective: To obtain a challenging and rewarding position in the

pharmaceutical or chemical manufacturing industry

that will allow me to utilize my current

and prior experience and offers

the potential for advancement in an

enthusiastic, growth-oriented

environment.

Education:

1990-1991 Crown College, Everett, Washington

Correctional Officer Training Program (Graduate)

1985-1987 Pasadena City College, Pasadena CA

Criminal Justice and General Study / Completed lower level

course work

Qualifications: Knowledge of FDA regulations 21CFR parts

210&211, cGMP and

SOPs, IQ (Instrument

Qualifications),OQ ( Operation Qualifications)

Experience as a department

safety rep, and a member of the

Emergency Response Team..

OSHA regulations and HAZOP Guidelines.

Strong written and oral

communications skills, detailed oriented,

reliable and very cooperative.

Work well with little or no supervision,

possess an aptitude to learn

new commodities and technical concepts.

Ability to work in a fast pace

environment.

Skills: All Windows platforms, Microsoft Office 2000, Microsoft

Word, Excel

Outlook and Data entry

Work Experience:

08/08-09/10 Sovereign Pharmaceuticals/ Quality

Assurance Specialist

7590 Sand Street Fort Worth Texas 76118

. Responsible for review and release of finished

product, review manufacturing and packaging batch

records and laboratory data to ensure accuracy and

cGMP compliance and FDA specifications. Approving and

releasing final product to be shipped.

. Follow production schedule and issue production and

packaging records to specified departments.

. Issue product labels and outserts to be used in

packaging process, reconciliation of labels and

outserts after packaging process is complete.

. Entering lot numbers and deviation reports into the

Master Production Log Book. Verifying validation

status, master batch records, forms and standard

operating procedure are accurate and current.

. Logging in-process, raw material and finished product

samples into the laboratory.

. Ensure that company procedures are followed.

. Maintain QA test results and assist with

determination of product specifications.

11/05-08/08 Adams Respiratory Therapeutics/ QA/

Manufacturing Technician

14801Sovereign Road Fort Worth Texas 76155

. Weighing, measuring and mixing of raw materials into

bulk batches of product. Operate process equipment

such as pumps, mixers, mills, homogenizers and

kettles. Equipment set-up and change over. Sanitation

of process equipment.

. Inspect production process, perform in process checks

of tablet compression, granulation, work up and

weighing of components. Batch record review for

completeness and cGMP compliance and calculation

accuracy for predetermined standards. Detailed

oriented and able to troubleshoot machines and

processes. Reach lift operator stand up forklift

operator and sit down forklift operator.

12/04-11/05 Baxter Bioscience/ Process Technician

4501 Colorado Boulevard Los Angeles CA 90039

. Performed procedures used in the production of Human

Blood Plasma to make synthetic blood.

. Filtrations, Fractionation and proteins separation.

. Column filtration and separation, centrifuge

separation.

. Performed aseptic cleaning on process equipment,

tanks, kettles, pumps and transfer lines to avoid

cross contamination, COP and CIP according to SOPs.

. Weighed and measured chemicals use in production

process.

. Computerized and physical inventory of chemicals

components.

01/98-12/04 Norac Pharmaceuticals/ Manufacturing Technician

405 South Motor Avenue Azusa California 91702

. Operate various types of equipment in the

manufacturing

of THC Tetrahydrocanabinol.

. High Pressure Liquid Chromatography and UV detection.

. Testings of in-process materials by Gas

Chromatography

. "Agilent GC".

. Density testing of solvents, Ph meter, Buchi Rotovap

distillation system for solvent recovery.

. Column filtration and separation of protein through

heat and vacuum distillation.

. Handle acids, pastes, powders, liquids and gels.

Adhere to ISO 9001 requirements and CFR 21 Parts

210&211.

. Sanitized and sterilized process equipment according

to SOPs

. Received incoming raw materials and shipped finished

products.

. Handled Lyophilized products and hazardous waste.

Contact this candidate