Engineer Manufacturing-Chemical

CORDELL L BRADLEY

*** *. ***** ** ***. ***, Long Beach, CA 90802 C: 510-***-**** **********@*****.***

PROFESSIONAL SUMMARY

[Chemical Engineer ] with [ 10 ] years of experience in [Biotechnology]. Areas of expertise include

[protein purification, HPLC, Assay development and cosmetics manufacturing ].

SKILLS

HPLC SmiSci PRO 2SDS-PAGE WordHomogenization processes

Power point Cosmetic Manufacturing ExcelProcess

C ontrol Assay Development

WORK HISTORY

Associate Research Scientist, 0 1/2008 to 1 0/2010 Oxygen Biotherapuetics Inc – Costa Mesa, C A

Responsibilities includes, Pilot scale manufacturing, process optimization and analytical testing

o fOxycyte(TM)(IV emulsion used for Traumatic Brain Injury) Responsible for the formulation of our cosmetics

brand, Dermacyte(TM) Oxygenating Concentrate skin cream Consultant for ContractManufacturing Facilities

during scale-up and large scale manufacturing for both Oxycyte(TM) and Dermacyte(TM) Help coordinate

stability programs for both Oxycyte(TM) and Demacyte(TM) Have written Stability Protocols, final Stability

R eports and Standard Operating Procedures.

QC Analyst III, 0 6/2005 to 11/2007 Tanox Inc – San Diego, C A

Initiated, perform, and assisted in Method Transfer and the Analytical validation of TNX-355 methods from our

Houston Facility to our San Diego Facility Assisted in setting up a functional QC Lab according to cGMP

guidelines Performed IQ/OQ/PQ on certain equipment in the Lab Trained other Analysts on methods

performed in the Lab Initiated new and revised Standard Operating Procedures (SOP's).

Quality Associate III, 0 7/2002 to 0 6/2005 XOMA (US) LLC – Berkeley, C A

Perform routine tests for the products our company develops, i.e(HPLC,SDS-PAGE,ELISA, DNAThreshold,

LAL, Nephelometry, Spectrophotometry and various wet chemistry assays).Assisted in various Assay

Development, Validation and Transfer procedures.Assisted QE in the Validation of equipment for Quality

areas.Wrote and modified Standard Operating Procedures (SOP's).

R&D Research Associate, 0 5/2001 to 0 7/2002 Glyko Inc – N ovato, C A

Developed new analytical methods by developing carbohydrate research for out-sourcing companies - - Xoma,

Mederex, Imclone, and BioMarin.Methods used were Flurophore Assisted Carbohydrate Electrophoresis,

(FACE) and Ion ExchangeChromatography Assisted in product development using chromatography for

separating carbohydrate sugars Assisted in the implementation of clinical trials Phase I, II, and III by using the

following techniques

QA/QC Analyst I, 0 7/1999 to 0 5/2001 Chiron Corporation – Emeryville, C A

Conducted investigative research and distributed reports on findings among senior management Involved

and lend support to in - process manufacturing to ensure quality of FDA approved products Performedvarious

analytical chemistry assays such as SDS-Page, BCA, Sialic Acid Determination, andFormaldehyde

Determination to ensure proper production of all manufacturing processes Responsible for determining protein

concentrations, aggregates and impurities by using techniques such as Reverse Phase HPLC, UV-Spectroscopy,

Anion Exchange Chromatography, and Size Exclusion Chromatography Developed various methods using

reverse phase HPLC and implemented those methods for new product development Responsible for the

preparation of numerous chemical reagents used in the laboratoryManaged all laboratory processes on a

quarterly basis, as well as distribution of work among team lab members Trained lab team members on the

following assays

EDUCATION

B.S : Chemical Engineering, C urrent Cal State Long Beach - Long Beach, CA

Emphasis in [ Petroleum and process control ]Top [5] % of class

2011 Long Beach City College - Long Beach, CA

A.A : Chemistry, Mathematics & Physics, 1 995 Laney College - O akland, CA

Laboratory Testing Experience: HPLC, GC, SDS-PAGE, ELISA, DNA Threshold, UV-Vis, Particle Size

Testing, pH, Osmolarity and other wet chemistry assays :

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