Quality Assurance Engineer
Resume:
Marc Averette
Miami, FL 33132
305-***-**** x74052
acdupe@r.postjobfree.com
RELEVANT SKILLS
• Certifications (April 2010): CompTIA A+, Network+, Security+, Microsoft MCSA/MCSE
• Proficient in MS Office, Excel graphing, Windows Desktop, HTML web page design
• Strong chemistry background and lab experience
• Familiar with writing and modifying SOPs
• Trained in GMP and FDA regulatory codes (worked in GMP/FDA facilities)
• Speak/read/write intermediate Spanish
PROFESSIONAL EXPERIENCE
Internal Controls Analyst
OneSale Miami Lakes, FL
October 2012 – December 2013
Create and maintain spreadsheets to analyze critical failure data and generate various
statistical reports and graphs. Write inspection reports, methods and standard operating
procedures. Create backups, maintain and continuously update vast electronic library of
inspection methods and historical data. Research and implement ways to improve
efficiency and eliminate procedural bottlenecks.
IT Technician
Broward County Supervisor of Elections Fort Lauderdale, FL
(Temporary assignment through AppleOne) August 2012 - October
2012
Performed maintenance, repairs and upgrades on hardware and software for voter
identification computers (Windows XP based systems)
Quality Assurance Technician
Perrigo Hollywood, FL
(Temporary assignment through Manpower) August 2010 - December
2011
Performed visual, strength, dimensional and leak testing on various blow-molded
bottles. Recorded all data using AQL sampling and GMP guidelines.
Research & Development Consultant
Virbac Animal Health Saint Louis, MO
May 2008 & November 2008
May: Helped setup manufacturing equipment, reformulated and aided with production
process and quality testing for several products.
November: Returned to fine tune process and troubleshoot various concerns.
Quality Engineer
EZ-Med Company Pompano Beach, FL
April 2002 - January 2008
Company was a nutraceutical manufacturer for the pet industry.
• Developed new product lines and improved existing ones by reformulating. Scaled up
formulas to production size.
• Wrote Standard Operating Procedures and operated equipment through entire
manufacturing process, from raw materials mixing to shipping of finished bulk
products.
• Kept and maintained logs and statistical graphs on product data.
• Performed various quality and shelf life testing on finished products before releasing,
such as water activity, hardness, microbe plate counts and heat aging.
• Designed and updated product labels, calculated data for ingredients listing order and
nutritional information. Packaged, labeled and shipped prototype samples.
• Set up and attended two annual trade shows.
• Created company website
Validation Engineer
Cordis Corporation Miami Lakes, FL
(Temporary assignment through Kelly Engineering Services)
May 2001 - February 2002
• Executed installation qualification, operational qualification, product qualification
(IQ/OQ/PQ) and test method validation (TMV) protocols for various equipment and test
methods that were used for the quality testing of their products.
• Aided in feasibility studies and design controls for regulatory requirements.
• Contributed to the site Test Method Validation Strategy Development as a member of
the four-man site TMV team contracted to codify nearly 800 tests for risk priority
analysis.
Materials Engineer Internship
SIMS Portex, Inc. Fort Myers, FL
May 2000 - September 2000
Company produces hundreds of injection, blow-molded and extruded plastic parts and
tubing for the medical industry.
• Performed trouble-shooting on different processes and characterization/design of
experiment studies for injection molded parts and IQ/OQ on machinery.
• Assisted R&D lab with environmental chamber testing and heat aging on a variety of
different polymeric materials.
• Performed dimensional analysis and strength (Instron) testing for quality assurance
and validation depts.
EDUCATION
Bachelor of Science in Materials Engineering (Polymers)
University of Florida, Gainesville, FL
REFERENCES
Available upon request
Contact this candidate