Bill G. Stockton
Fox Lake, IL 60020
abhlyu@r.postjobfree.com
SKILLS
• Over nine years experience working in a cGMP manufacturing facility.
• Knowledge of numerous types of laboratory and pharmaceutical production equipment including but
not limited to: autoclaves, process tanks, incubators, and analytical equipment and CIP/SIP systems.
• Knowledge of basic chemical and biological safety procedures.
• Good computer skills, knowledge of Microsoft Word, Excel and Outlook
• Good interpersonal skills and be able to work effectively and efficiently in a team environment
• Proficient in a variety of mathematical disciplines compiling mathematical calculations for Batch
Records
PROFESSIONAL EXPERINCE
2010-Current GE Healthcare Production Technician II
GE Healthcare manufactures Radiopharma drugs. Some of GEHC core strengths include Biosciences,
technology and diagnostic equipment.
• Experience formulating pharmaceutical/ radioactive pharmaceutical dosage forms (Solid and
Parenteral) including Tablets, Encapsulation and sterile Injectable drugs.
• In-depth knowledge of cGMP and GLP guidelines pertaining to pharmaceutical and diagnostic
research manufacturing.
• Dispense final product radiochemical and radiopharmaceuticals from raw materials in accordance
with regulatory requirements i.e. current Good Manufacturing Practices (cGMP)
• Trained on all aspects of radioactive safety that abides by OSHA rules and regulations, including
both state and federal regulations
• Formulate and package Radiopharma drugs including Iodine 123 and Thallious Chloride.
• Ensure all GMP documentation is complete and accurate and in compliance with 21 CFR 210,
211 and 11
• Perform various other activities include the preparation and sterilization of vial filling apparatus.
• product.
• Accurately review and complete all batch records and related documentation.
• Assist in writing Investigation Reports and initiate unscheduled work orders
• Operate and maintain depyrogenation ovens and autoclaves along with connected chart
recorders.
• Work in and operate equipment associated with the printing and labeling of product.
• Respects all aspects of the 5 S Lean way of laboratory and manufacturing operations.
• Trained and passed all requirements for wearing all respirator equipment.
• Works together with Quality, Chemistry, and Microbiology departments.
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Bill Stockton Resume
2008 – 2010 Catalent Chemical Handler/Formulator
Catalent a global leader in drug-delivery technologies, contract manufacturing, packaging and product
launch services. With seven decades of experience and over 1500 patents and patent applications,
Catalent brings its customers innovative expertise throughout a drug’s development, launch and entire
lifecycle.
• Worked as Chemical Weigher Formulator in Sterile Pharmaceutical Manufacturing.
• Performed formulation, chemical dispensing, Cycle count for chemicals and filters.
• Performed inventory investigations report for chemicals variance.
• Trained new personnel in chemical dispensing area.
• Conduct yearly physical inventory for chemical and manufacturing area.
• Worked closely with Kaizen team to resolve all known issues in a timely manner.
• Developed strong operational functions in the stockroom such as cycle count chemical inventories,
using J.D.Edwards soft ware.
• Respects all aspects of 5 S Lean manufacturing.
• Assembled and operated filtration systems.
• Passivate and steam in place various formulating equipment using hazardous chemicals.
• Operated general production equipment (such as pH and conductivity meters, autoclave, and
portable mixer.)
• Monitored and recorded critical process parameters using chart recorders and aseptic room pressure
gauges
• Completed all relevant paperwork following GDP/GMP guidelines.
• Performed routine maintenance and cleaning of production equipment.
• Performed sampling using aseptic techniques that are submitted to micro and chemistry departments.
• Worked with environmental monitoring equipment.
2007 – 2008 Nanosphere Laboratory Technician
Nanosphere, Inc. is a nanotechnology-based molecular diagnostics company, offering proprietary
breakthrough technologies that provide a unique and powerful solution to greatly simplify
molecular diagnostic testing
• Performed assay development activities.
• Designed, screened, and optimized antibody’s based detection assays.
• Prepared reagent development and testing.
• Document results in compliance with Good Laboratory Practices(GLCs)
• Compiled results for monthly reporting including, temperature gauges, charts for incubators,
freezers and refrigerators.
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Bill Stockton Resume
2006-2007 Baxter Healthcare Scientific Technologist
Baxter International Inc. is a global healthcare company that, through its subsidiaries assists
healthcare professionals and their patients with treatment of complex medical conditions including
hemophilia, immune disorders, kidney disease, cancer, trauma and other conditions
• Remain current with new and revised manufacturing procedures
• Completed relevant paperwork following GDP/GMP Guidelines
• Required a solid understanding of QA/QC requirements including strong knowledge of 21 CFR
210, 211 and 11 and other regulatory requirements, GCP’s and GLP’s
• Worked pilot plant setting
• Aseptic Gowning Certified
• Operated general production equipment such as Ph and conductivity meters, homogenizers
and various equipment related to Isolators and Aseptic areas
• Performed routine maintenance and cleaning of production equipment to encure compliance
with cGMP’s
2004-2006 Dentsply Pharmaceutical Manufacturing/Distribution
Dentsply manufacturer of injectable dental products
• Certified Aseptic Operator
• Certified in cGMP’s, sanitization and gowning procedures
• Operated and sanitized Bausch & Strobel filling machine
• Prepared cleaning solutions
• Restocked aseptic materials,
• Performed loading and unloading of sterilizers
• Worked in compounding, component preparation and bottle wash areas
• Conducted inventory control/distribution, inspection and packaging operations
2002-2004 CSL Behring Pharmaceutical Manufacturing Operations
CSL Behring is a highly sophisticated pharmaceutical manufacturing site-manufacturing
products derived from human blood plasma.
• Worked in the Aseptic environment making life saving/injectable liquid and lyophilized
products
• Performed operations in compliance with FDA, EU and OSHA standards
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Bill Stockton Resume
• Certified in cGMP’s, sanitization and gowning procedures
• Highly trained to sanitize all surfaces and fixtures with caustic chemicals
• Worked in Coagulation and Fractionation departments using human blood plasma as the
raw material.
• Sterilized parts, surfaces and equipment using water for injection, (WFI)
• Highly trained in heat steamed water, mixed with various chemicals, cleaning techniques
• Worked in maintenance and sanitation departments
• Recorded batch records and pharmaceutical documentation, e.g., SOP’s, policies and
procedures
1998-2002 Monsanto, Equal, Nutra Sweet Distribution/Manufacturing
Manufacturer of Equal, Nutra Sweet food product
• Responsible for training new associates on different aspects of logistics and warehouse operation
• Worked as a Lift truck operator in the warehouse trailer spotter and manufacturing
• Trained employees in all cGMP’s, SOP’s and GDP guidelines
1990-1998 Sears Logistics Distribution Supervisor/Trainer
• Supervised approximately 15 associates in distribution activities
• Trained associates in classroom and on the floor on the proper use of warehouse equipment,
using OSHA regulations and cGMP’s as guidelines
• Worked in all capacities of warehouse distribution including, shipping, receiving and trailer
spotting
EDUCATION:
• High School/GED
• PC/Tech Certified
• Attended Kankakee Community College