Deborah A Hubbard
San Leandro Ca. 94577
•Familiar with GMP’s for manufacture processing, storage holding of drugs and finished pharmaceuticals. Lab testing of adhesive products.
•Resolve issues by the use of GMP’s and company guidelines. Deviation investigations, compliance reviews, Documentation reviews. Document Control,
•Proficient using MS Word, and Excel.
•Installation of medical devices, and in vitro diagnostic products Familiar with SPC, SAP and LIMS systems, Surface plate inspection, GD&T, optical comparators Quality System Registration ISO 13485, clean room environment, CMM testing controlled by metrology. calipers, radius gages, thread gages, pin gages, metal classifications, micrometers, Oscilloscope, CAPA’s, NCMR’s, batch records, line clearance, BOM’s, Microsoft word, PowerPoint, Excel, 1st Article Inspection, mechanical inspection, ISO 9001:2000 Quality System Registration 08/01/2002, licensed to transport explosive materials
PROFESSIONAL EXPERIENCE: *QC Lab Technician
*Pharmaceutical/ Inspection Technician
*Mechanical Explosives Inspector II
*Quality Assurance Coordinator
January 2014 to Present
QC Lab Technician
•Quality Lab Technician responsible for working with business and technical staff in planning, executing, and documenting testing, while promoting a safe work environment.
• Lab testing of adhesive products.
•Testing adhesives using a spectrometer to get the concentricity of the chemical ingredients of the product. Determine the percentage of its dicyandiamide (dicy), I.R testing.
•Testing of Film Carrier Weight and Resin Content analysis calculations of different templates size. Using THF or Methanol solvent chemicals.
•Viscosity measurements to test the movement of liquid in adhesives under certain conditions with using a Rheometer tester.
•Mixing hazardous chemicals used for testing adhesives.
•Disposing of hazardous materials, and chemicals.
•Document test cases to meet desired test coverage goals.
•Work to minimize risk by identifying, communicating and escalating issues appropriately to management.
YOH/ A DAY & ZIMMERMANN COMPANY August 2012 to December 2013
Pharmaceutical/ Inspection Technician, Genentech (Contract)
•Responsible for the final inspection of necessary medical products using Current Good Manufacturing Practices (GMP) while maintaining the production schedule.
•Communicate quality issues and complete discrepancy documentation as required in a timely manner.
•Strong organizational skills with the ability to resolve issues and adapt to changing priorities.
PACIFIC SCIENTIFIC May 2008 to August 2012
Mechanical Explosives Inspector Level II
•Inspection of energetic explosive materials and devices for the defense industry.
•Production environment auditing.
•Explosive devices and material auditing.
•Perform limited repetitive dimensional and electrical inspection using basic equipment and established procedures with minimum supervision.
•Interpret drawings and written work instructions.
•Use of a variety of precision measuring instruments.
•Familiar with metal classifications
CUMMINS-ALLISON August 2005 to June 2007
Quality Assurance Coordinator
•Review and process receiving inspections using Supplier Focus.
•Resolving issues regarding quantities, receiving condition of products.
•Creating and maintenance of various spread sheets, printing reports through excel.
•Manage documents and document changes
•Coordinate inspection assignments with Quality Inspectors and team leaders.
•Processing Certificate of Assurance with LIMS 6.
A.L. HANSEN August 2000 to January 2005
•Auditing manufactured parts.
•Incoming inspection of mechanical machined parts.
•Visual, dimensional, and cosmetic inspection.
OTHER PRIOR EMPLOYMENT: Opportunity Medical
Rank Video Services of America
Associate of Art, Communications
Minor Music: General with Honors