Dianne McCammon

**** *. ****** *** *******, CA **776

Home 626-***-**** Cell 805-***-****

dk2ocn@r.postjobfree.com & dk2ocn@r.postjobfree.com

Objective

I’m interested in a long-term full time position in any of the position listed below. I will relocate, and am willing to travel up to 75% of my time. A list of references and letters of recommendation from my last employer can be provided.

Summary of Qualifications

Quality Assurance, ISO 9002 - Document Control Manager, for medical and high-tech. manufacturing companies.

Facilities and Civil Engineering Tech.

Human Resources Program Manager, Supervision and Training.

Management Administrator and Budget Analyst.

Employment

WePackItAll, Duarte, CA; Quality Assurance/Document Control Specialists 01/2008 to 05/2010

WePackItAll is a FDA, ISO, GMP, HACCP certified manufacture, specialized in packaging. I was there first fulltime Document Control Department Specialist. I conducted employee training sessions and supervised one person. Their main products were food supplements. While I was there they branched out into Organic, Kocher, and Hypo-Allergenic Foods. I also, saved the company $600,000.00 in product and legal costs.

• Restructured filing systems hard copy and electronic.

• Updated the Quality Control Systems Manual and Quality Control Procedures Manual.

• Created data base tracking system for in-service, archived and working documents.

• Worked with management to update, consolidate and create new SOP’s.

• Created and enforced a review system for SOP’s.

• Created and paperless security files for all SOP’s.

• Did safety inspections out on the work floor and on offsite warehouse.

• Created and tracking data based for all CAR and PAR’s.

• Managed and all hard copy CAR’s and PAR’s.

• Managed all hard copy supplier files.

• Maintained all private employee training files and tracked system.

• Maintained, updated and created internal forms.

• Tracked and audited all equipment cleaning forms.

• A part of the H ACCP management core team, on 24 hour call.

• Tracked and approved all job issuance before going to the work floor.

• Worked closely with Marketing Department on job orders.

Was laid off along with 10 other middle management employees

Celite /World Minerals, Lompoc, CA; Quality Control Lab/Document Control 10/04 to 07/2007

Celite is the world’s only salt water diatomaceous earth mine used for filtration.

Quality Control Lab: International Standards Organization (ISO) Document Control Coordinator.

• Responsible for working with the department heads to help organize and prepare them for ISO internal and external audits.

• Managed all controlled documents and archives electronic and hard copy; Standard Operating Procedures (SOP’s) Lab Test Methods, Test Levels, Records, Forms, Department Audits, Quality System Procedures Manual(QSPM) and Quality System Manual (QSM), Corrective Action Reports (CAR’s) & Preventive Action Reports (PAR’s).

• Responsible for final review of changes in; content, formatting, numbering, revision, issuance, and distribution to meet the requirements of the ISO9002 Quality System.

Position was eliminated after company was sold to Imerys, a French multinational company.

Dianne McCammon

5218 N. Burton San Gabriel, CA 91776

Home 626-***-**** Cell 805-***-****

dk2ocn@r.postjobfree.com & dk2ocn@r.postjobfree.com

Continuation

Pacific Bell/SBC Services, San Ramon, CA. Financial Quality Control 3/99 to 10/01

Member of LROCC Task Force for Leased Computer Equipment Returns.

• Troubleshooter for offsite inventories and audits for returned leased computer equipment in 12 mid-west states. Member of the Core Budget Group for the Department. Personally recovered $300,000.00 in lost or unlisted leased computer equipment.

• Created a database tracking system. Reconciled old and new assets against the LROCC Assets Tracking Database to 100% reconciliation on a daily bases.

Department moved to Dallas, TX. I could not move for family reasons.

OUR Medical Systems, Pleasanton, CA. Quality Assurance/Document Control 3/98 to 3/99

Gamma Knife Medical Equipment, manufacturer, gamma rays surgery on brain cancer patients.

• Enforced strict manufacturing standards using ISO 9001, Blue Prints, CARS & PARS, Supplier Audits, SOP’s, maintained FDA regulation Binders, as a part of the GMP standards.

• Developed and implemented a new Document Control data base for their Control System.

• Worked directly for CEO, VP of Operations Engineering, VP of Quality Assurance.

(Start Up Company, lost funding and went out of business)

Seimens Medical Systems Oncology Care Systems Groups, Concord, CA 10/95 to 10/97

Manufacture of “The Magnetom” a tumor dignity and location diagnostic equipment.

ISO Document Control/Quality Assurance Technical Analyst.

• Worked with department heads on managing all design changes and additions to blue prints and engineering design documents.

• Responsible for sending and tracking all Supplier SCAR’s & SPAR’s.

• Created and maintained Change Control Data Base and hard copy archive.

• Maintained departmental procurement, Supplier Classification Restrictions, Supplier Material Rejection reports.

+Left for a job closer to home and family.

U C Davis - BS, Native American Studies

Computer Program Expertise

MSWord XP MS Vista

Excel Power Point

QuickBooks Lotus

Outlook Auto Cad/Road Design

Cartographic Critical Logistics Analyst

Oracle Financials Tutor Author/ Publisher

Citrix Intelx- DC

Access LIMS

Management Classes

Nuclear Gage Management

Administration Management

Regional Leadership Training

Women in Engineering

ISO 9001:2000 /Continuous Improvement

HR Special Emphasis Program Manager

Quality Assurance Control Management

Business Administration Management

Finance Management

Contact this candidate