Tami Brittingham

*** ****** **

Wilmington Delaware 19804

302-***-****

ad1zty@r.postjobfree.com

EDUCATION:

****-**** ******* **-**** Major (Technical Drafting)

****-****. ***** ********* ******* (Nursing LPN)

2006-2007 Harris School of Business (Surgical Nurse)

2008 -2009 Argosy University (Pursuing Bachelors Degree in Art of Psychology)

EMPLOYMENT:

August 2019 – June 2021

Weekend Production Supervisor – Exide Technology – Lancaster, PA

This was a full time position Supervising on the weekend off shift. All duties consist of Following “Leader Standard Work” to ensure daily, weekly and monthly tasks are complete., Directs and supervises all employees and production in the assigned area, Maintains production and quality standards as directed by plant manager, Checks and maintains production reports and enters production into JDE daily, Meets daily with employees to ensure good communication is maintained on all issues in department and the plans. Completes production and scrap reporting, Reports any shortages of supplies or equipment required for daily operations, Schedules employees assigned to area, Trains, instructs and supervises new employees on job operations, until employees meet job requirements, Evaluates employee’s job performance in relation to established production standards, Counsels employees on job performance, safety/health, absenteeism, tardiness, and disciplinary issues, Interviews applicants to fill appropriate job openings after initial screening by Human Resource Department, Mentor associates and team leads, Participate and or leads in training, development, and certification programs, Ensures all employees follow health and safety guidelines and wears proper PPE in department, Responsible for working with employees to reduce their blood lead and eliminate accidents within departments, Checks and verifies employee’s time in the Kronos Timekeeping system for accuracy prior to approving for weekly payroll processing, Enter employee schedule and changes same for tracking., Participates and supports Lean programs in department and the plant, Follow health and safety practices as they apply to work and the facility and supports STOP program.

May 2016 – August 2019

Quality System Administrator – B&W Tek Inc – Newark, DE

This was a full time position in which I performed all the listed duties. Manage and administer the following processes as they relate to the facility, Product drawings and data sheets, work instructions, Standard Operating Procedures – SOP’s, Forms, Document updates, proofing, distribution and notification, Document Change requests (CR’s), Engineering change orders (Co’s), Non-Conformance Reports (NCR’s), Return Material Authorizations (RMS’s), Record Retention and maintenance, CAPA’s, Internal Audits, Work independently to perform ongoing review of quality systems and procedures in order to identify and recommend revisions to current systems and new systems, Initiate and implement modifications and the improvements to control documentation such as production check lists, Final Quality Control (FQC) records, operating procedures and policy manuals, Communicate with suppliers, as necessary, to obtain RMA’s and CAPA statements, Maintain safe work area in a clean and orderly condition, and Perform all other duties as assigned by management.

August 2013 - May 2016

Quality Administrator/Supervisor - AMI Metals – Swedesboro, New Jersey

This was a full time position working in a sheet, plate, and extrusion warehouse. These metals are used for all military and commercial aircraft. My duties include all vendor discrepancies, internal discrepancies, credits, and corrective actions. My duties also include all floor inspections, (incoming, in process, and before its released inspections) responsible for training all manufacturing employees on QP’s, updating procedures, ranges, reviewing work orders and expediting them, checking on export license approval, and customer issues.

August 2012 – August 2013

QualityAssurance:Technicians - Terumo Medical Corporation Elkton, MD

This was a temporary position which I performed all incoming inspections of Bipore and Destination medical devices. My responsibilities included instron and tensile testing, 3 point bend, operating and testing on the CMM and OGP, review of all DHR & AQL sampling, measurements using a variety of gages and laser mikes, (pins, luer taper, etc).

December 2009 – August 2012

Quality Coordinator, Document Control, Internal ISO Auditor Rexam Newark, DE

This was a full time position which all responsibilities were based on Quality for a Plastic Injection Molding Company. I performed the scheduling for all the daily functions in the quality

department, investigations on cause of rejected or returned product, customer complaints, updating and writing of new procedures, testing and programming the CMM and OGP, internal ISO audits, implemented TMS, and kept all Rexam employees up to date in all training.

October 2007 – December 2009

Manufacturing Technician Research and Development - W.L. Gore and Associates - Elkton, MD

This was a full time position which my responsibilities were in research and development of balloon catheters for cardiovascular. Worked closely with engineering to validate machines and process ER’s (engineer request) for device builds. Worked in lab for testing devices for compliance to burst, leaking and ran the tape wrapper to make the gore-tex material and various other machines.

March 2005 – October 2007

Production Supervisor for Packaging of Pharmaceuticals - Cardinal Health Inc. - Philadelphia, PA

My responsibilities were to oversee 75 to 100 union employees on the off shift hours included hourly inspections, testing, validating of all production lines, employee reviews, and performance feed backs.

March 2004- March - 2005

Quality Technician for Packaging of Pharmaceuticals

-Cardinal Health Inc.-Philadelphia, PA

My responsibilities were performing in-process and finished product inspections, validating and line clearances for Manufacturing and Packaging Operations, review all appropriate documents for production runs, including the review and approval of batch records prior to close out, and doing a complete inspection of production room after change over to sure no loss pills were left from previous jobs to release room to start next batch. (The above job was a transfer still within Cardinal Health)

May 1993 – March 2004

Quality Technician - DuPont Dow Elastomers LLC/Kalrez - Newark, DE

My responsibilities included cycle counting, molding, lathing, milling, extrusion, finishing and inspection of fluoroelastomer o rings. Took on 6 Sigma Project and took charge of all small O-Rings and Roll Flow. Head quality inspector and lead trainer for finishing department.

May 1990 – May 1993

Manufacturing - Technician –Pencader DuPont - Newark, DE

My responsibilities were the making of carbon fiber veins for military jet airplanes. This entire process was done from start to finish. From cutting the prepreg on a die cutter, usage of a 300 and 400 ton press, sanding the finished product with a drummel, final inspection, and government stamping it to be shipped to Boeing and other military bases. (The above job was a transfer still within DuPont)

OTHER EXPERIENCE:

FDA, CGMP, Six Sigma,

Safety Committee, SAP, JD Edwards, Certified in Tech Drafting, Certified in First Aid and CPR, ISO Audit Training, Implemented TMS, CMM Training.

TOOL AND MACHINE EXPERIENCE:

A variety of Calipers, Comparators, micrometers, CMM, OGP, Misc.Gages (Snap, Thread, Height, etc.) 300 and 400 ton presses, Extruder, 4 arm tarot lathe, CNC, Etc.

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