Brian J. Starbuck
***** *. ******** ******, *********, CO 80111
Home: 720-***-**** *********@***.*** Mobile: 303-***-****
Versatile Chemist highly experienced in a variety of industries with highly developed business acumen
Scientist strongly motivated by the improvement of products through innovation and invention of
new manufacturing products for market. Highly developed science acumen across multiple
disciplines. Possess 15+ years experience in chemical production operations, chemical analysis,
evaluation of materials for fitness of use, and project management. Polished skill with integration
of fiscal, regulatory, logistics, engineering, and quality functions. Experienced implementer of Six
Sigma and lean manufacturing principles. Skilled written and verbal communicator, with proven
ability to collaborate with customers and colleagues to solve problems and implement efficiencies.
Strong bottom line and enterprise awareness, resulting in ability to innovate and deliver products
and services to customers, management and investors.
Logistics Personnel Process management
s s s
management
Statistical process Technical sales
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control Customer service Organic chemistry
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MS Office Suite Analytical chemistry
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PROFESSIONAL EXPERIENCE
Modec Inc., Denver, CO 2007 – 2012
CHEMICAL PRODUCTS MANAGER
Manufacturer of licensed decontamination products, applications and materials used in
remediation of chemical weapons and biological pathogens, toxic industrial chemicals, molds and
viruses. Developed and performed complete product lifecycle management and process
standardization of decontamination product. Initiated Just In Time manufacturing operations that
functioned profitably, safely and delivered product quality improvements. Invented numerous new
product applications.
Managed product data development with testing laboratories and completed EPA regulatory filings
for label and efficacy claims. Conferred with regulatory consultants and federal and state
regulators on submission of Confidential Statement of Formulations, label language/format and
developmental strategies.
Expanded customer base and international markets through representation at trade shows and
other high contact customer venues. Developed and trained sales staff on product value
propositions. Designed product labels and consulted with web designers relative to acceptable
content and claims.
Singlehandedly completed 3,000 gallon per month production rate of a liquid binary product,
attaining revenues of over $105,000 per month and gross margins of over 50%.
Managed multiple regulatory compliance submissions for pathogens, including laboratory
testing protocols and correcting testing errors. Developed testing protocol for Norovirus
efficacy testing followed by approved EPA submission.
Successfully instituted and commissioned in house chemical engineering processes to
ensure integrity of batch records and attain benchmarks necessary for regulatory
compliance.
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PROFESSIONAL EXPERIENCE (CONTINUED)
Nanoproducts, Longmont, CO 2003 – 2007
CHEMICAL MANAGER
Patent holding manufacturer of nanometer sized metal oxide powders. Oversaw cross functional
team challenged to develop precursor to manufacturing formulations and critical property data
needed to establish plasma based manufacture. Identified and eliminated root cause of non
performing powders. Operated argon plasma based production process. Developed and
performed analyses and product quality measurements for classification of nanomaterials
including BET analysis, SEM analysis and rheology.
Managed a complex blending/synthesis operation with zero safety incidents.
Gained promotion to Chemical Manager from position as Chemical Process Operator, due
to depth of knowledge regarding process to precursor, and initiative taken to improve
speed and efficiency of experimental methods.
Orica Commercial Explosives, Watkins, CO 2000 – 2002
GROUP LEADER PACKAGED PRODUCTS
World’s largest manufacturer of commercial explosives. Directed developmental engineering and
four staff in improvement of commercial explosives. Completed thorough hazard operation review
evaluations. Investigated field performance and resolved product complaints directly with
customers.
Conducted an over one ton product trial that implemented a proprietary product design
innovation, then designed and executed product evaluation program.
Implemented improvements in plants in North, Latin and South America, resulting in cut
costs and improved margins.
Rosemont Pharmaceuticals, Denver, CO 1997 – 2000
RAW MATERIALS QUALITY CONTROL MANAGER
Manufacturer of 20 generic pharmaceuticals owned by Akzo Nobel. Managed 5 quality control
personnel and laboratory resources. Oversaw quality control of 100 to 200 raw materials for
finished dose pharmaceuticals in a FDA protocol/Current Good Manufacturing Practices (CGMP)
environment. Conducted analyses, out of specification inquiries, and unit operation quality
measurements. Collaborated with operations and purchasing to ensure material readiness.
Applied Statistical Process Controls to plant wide deionized water system and
recommended corrective actions, achieving ongoing plant operational readiness.
Previous background includes experience as Staff Chemist at a commercial laboratory performing
complex syntheses, natural product isolations and purifications, support for legal actions, and
material evaluations; and as Chemical Materials Engineer at National Semiconductor working with
fabrication engineers to implement statistical process controls.
EDUCATION & AFFILIATIONS
Oregon State University, Corvallis, OR MASTER OF SCIENCE DEGREE, CHEMISTRY
Colorado State University, Fort Collins, CO BACHELOR OF SCIENCE DEGREE, CHEMISTRY
American Chemical Society, Member