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Manager Quality Control

Location:
Athens, GA
Posted:
December 31, 2013

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Resume:

PRODUCTION SUPERVISOR

Patricia Seaberry

*** **** **. ******, ** 30605

E: *********@*****.***

C: 510-***-****

Professional Summary

Dynamic operating / management professional offering extensive and

successful leadership position in industrial and manufacturing areas.

Cultivates a company culture in which staff members feel comfortable

voicing questions and concerns, as well as contributing new ideas that

drive company growth.

Skill Highlights

Operation Start-Ups Shipping & receiving

operations

Quality Control and customer / client relations Project troubleshooting

& problem resolution

Team leadership and staff development OSHA regulations and code

compliance

Time management; deadline sensitive Inventory management-

JIT system

FDA CLIA & CGMP Standards ISO Standard

Human Resources Budgeting

Production Control Performance Evaluations

Multi-task - Oriented SAP / DMS/ EQUE / ADP

Professional Experience

Assistant Manager

Biotest Pharmaceuticals - Athens, GA

2010 to 2013

Start -up. Appropriately resolved customer issues, complaints and

questions. Provide valuable health-care counseling. Followed state and

federal record keeping guidelines for FDA approved Standard Operating

Procedures, OSHA, and CLIA. Safely administer immunizations for Rabies

specialty program. Maintained proper inventory levels, rotated stock.

Directed operations to increase efficiency and minimize patient wait times.

Use SAP to compile and submit orders to vendors to meet determined

inventory levels

Assistant Manager

Talecris Pharmaceuticals - Salem, OR

2008 to 2010

Assist with operational management of a Plasma Collection Center,

Compliance with all applicable policies and regulations. Act on behalf of

Center Manager in her absence. Supervise donor selection, plasma

collection, shipment, and record completion. Build rapport with donors to

ensure overall customer satisfaction. Maintain compliance with state and

federal regulations, U.S. Food and Drug Administration (FDA)-approved

Standard Operating Procedures, Occupational Safety and Health

Administration (OSHA), Clinical Laboratory Improvement Amendments (CLIA),

and Current Good Manufacturing Practice (cGMP). Schedule all employees to

accommodate donor cycles. Collaborates with Training and Quality staff to

ensure that training and quality goals are met and to implement operational

changes and maximize center efficiency. Leader and coach through effective

feedback to employees. Identify regulatory deficiencies and implements

immediate corrective action. Investigate all unsafe situations and

complaints.

Quality Supervisor

Biomat USA Incorporation - Phoenix, AZ

2007 to 2008

Expertise in cGMPs, FDA regulations, SOP implementation, and an

understanding of quality control principles and QA audit function. Prepare

for Internal and external quality driven audits. Assist in hiring of new

employees, Maintain Quality Certification. Prepare samples for courier

pickup. Monitor training documents. Follow-up and track corrective

actions for preventive measures, Update the Center Procedure Manual with

the most recent approved procedures and forms.

Quality Assurance Technician

Syntax Brillian- Scottsdale, AZ

2001 to 2007

Inspection techniques and measurement of micrometers, calipers, pin gages,

OGP, XY table, etc. Disposition incoming discrepant materials, Maintain IQC

inventory of incoming, outgoing, and Non-conforming materials. Maintain

required logs/records, for ISO 9001:2000 for all inspected material.

Generates and distributes reports, charts and office correspondence;

regarding defect trends. Performs quality inspections on raw materials, in-

process goods and finished product according to drawings, SOPs, standards,

as appropriate.

Process Engineering Technician

Lam Research Corporation - San Jose, CA

2000 to 2001

Write recipes for 200mm SAC and HARC processes on the Exelan HP. Metrology

support - Hitachi Sem, x-section and CD SEM measurements. Thin films

support using Prometrix tool and Dektak 8000 profiler. Manually cleave and

decorate 200mm wafers in wet lab. Denton Vacuum Desk 2 equipment to coat

wafers. New part validation, characterization, and release to production.

Complete weekly process qualifications. Prepare baseline on different

gases to run process marathons. Implement process change by writing IPCN'S,

DCN'S, SWR'S, and STRS for engineering experiments.

Senior Quality / Reliability Technician

Motorola Semiconductor - Chandler, AZ

1981 to 2000

ASICs, DRAMs, Flash, EEPROM, SRAM, and CMOS Devices. Positive and

negative photoresist, materials used in photolithography to transfer

pattern from mask onto wafers. Dry ( RIE, ICP, Plasma - Anisotropic ) &

wet chemical solution Isotropic etching (nitric & hydrofluoric acid).

Disposition material discrepancy lots, implement SWR'S and Process changes

as needed. Engineering projects to help ensure HIP6L Nitro XC

Qualification in MOS 13, which was qualified ahead of schedule. Analyzed

engineer and low yield production lots through generating wafer maps, Unit

and Parametric Probe data. Proficient software usage; KNIGHTS, SAP, EDAS,

DART, DATALOG, SYNERGY, PROMIS, PROBE, CANVAS, FILEMAKER PRO, JMP UNIX DOS

WINDOWS NT EXPLORER, MICROSOFT WORD, EXCEL, and POWER POINT. Analyzed low

yield production and engineering lots through generation Wafer Maps, Unit

and Parametric Probe data. Retrieve daily Trend charts, monitor watchdog

results, and disposition material discrepancy lots. Evaluate Statistical

Analysis on engineering experiments through generating Cumulative Percent

Plots, Time/Equipment commonality, Wafer maps, Unit and Parametric Probe

data. Implementing process changes by writing IPCN'S, DCN'S, SWR'S, and

STRS for engineering experiments. Perform Reliability stress test

(Operating Life, Temperature Cycle, Thermal Shock, and Auto Clave) on ASIC

parts using various ovens and environmental stress chambers to ensure the

integrity of the test. Preventive maintenance and cleaning environmental

stress chambers. ISO9001 Compliance Documentation, Create and revise (PCN)

Process Change Notices. Build, repair, and solder of test fixtures.

Maintenance Supervisor

WHITE OAK SEMICONDUCTOR (JOINT VENTURE) Motorola / Infineon - Richmond, VA

1997 to 1999

START UP, Mark Scan and Pack, Burn-In, and Final Test Maintenance

Supervisor. Employee Performance Evaluations, Promote communication and

cooperation between shifts. Thoroughly communicate status of operations at

shift change. Projects and process improvement team leadership. Meet

department/company goals and objectives. Train technicians. Promote career

development. Preventive maintenance, diagnostics procedures on Schluberger

300 and Sipa Pick and Place Handlers, ANDO and AEHR ovens, ADVANTEST &

Mulhbeur testers and handlers, Mark Scan and Pack Tape and Reel machines,

ROOD Lead Conditioner, and Sealer for package devices. Written controlled

technical specification procedures.

Education and

Training

Associate of Science: Computer Science 1983

Miller Institute of Technology - Phoenix, AZ -USA

High School Diploma: General Studies 1980

Westwood High School- Mesa, AZ -USA



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