ERIC F.

ABDELLA
7324 Cascade Ct. Apt 1034
Fort Worth, TX 76137
515-401-8753
Efflux@hotmail.com

CAREER OBJECTIVE
Employment position that offers challenge and opportunity for future growth.

EDUCATION
Ferris State University, Big Rapids, MI.
Earned Bachelor of Science degree in Pharmacy in December 1988.

Michigan State University, East Lansing, MI.

Earned Bachelor of Science degree in Medical Technology in June 1985.

Michigan State University, East Lansing, MI.

Earned Bachelor of Science degree in Physiology in August 1984.

WORK EXPERIENCE
Jan.2008-May 2010
Cambrex, Inc. Charles City, IA. Analytical Development Department
Sr. Analytical Development Chemist
Development, validation, and method transfer of a variety of analytical test methods for an active pharmaceutical
manufacturing facility. Participation in project teams as analytical development department representative to
perform duties such as coordination of analytical needs, customer interaction, analytical testing support for
chemical development department, and ensuring the components of a project have requirements necessary from
an analytical development perspective. Assay, residual solvents, and impurity method development, cleaning
validations, and validation of methods for use on a wide range of instruments (HPLC, GC, HSGC, dissolutions,).
Method validations on new compounds, existing compounds, in process manufacturing of active pharmaceutical
ingredients, and manufacture release testing of active pharmaceutical ingredients. Writing protocols, validation
reports, analytical test methods, and standard operating procedures.

Dec.2002-Dec. 2007
Qualis, Inc. Des Moines, IA. Technical Services Department
Analytical Method Development/Validation Chemist
Development and validation of various analytical methods for current and new product formulations. Method
validation protocols, study report, and test method composition. Execution of method validation protocols.
Analytical method problem solving. Primary focus on LC, GC,FTIR method development and validation. Cleaning
validation method development and validation. Additional responsibilities include maintenance and operation of
stability department. Stability sample receipt, labeling, disposition in long term stability chamber or accelerated
stability ovens, sample log into spreadsheet for testing schedule, sample pulls at required time intervals,
specification sheet issue, evaluation of test results, and final study report preparation/submission.

Nov. 1998-Dec.2002
Accra Pac Group, Inc., Elkhart, IN.
Technical Services Department
Sr. Analytical/Validation Chemist
Quantitative analysis of a variety of liquids, creams and aerosol products using HPLC, GC, IR, UV, and AA
techniques. Analytical method development, method validation, and method transfers according to GMP and FDA
guidelines. Cleaning validation protocols, cleaning method validation and development. Extensive recordkeeping,
problem solving and various other lab responsibilities.

March 1992-Nov. 1998

Leiner Health Products, Kalamazoo, MI.
Quality Control Department, Lead Chemist.
Quantitative analysis of vitamin supplements and OTC drug products, raw materials and intermediates by way of
HPLC, GC, AA, UV, and IR methods. Formula adjustments, extensive record keeping and documentation,
employee training and various other lab responsibilities.

Sept 1990-March 1992

International Research & Development Corp., Mattawan, MI.
Analytical Chemistry Department, Analytical Chemist.
Analysis of test material diet preparations using HPLC, spectrophotometry and thin layer chromatography.
Method development, method validation, recording, review, and reporting of analytical results.

ADDITIONAL EXPERIENCE
Vast computer experience using Windows, Microsoft Office, and a wide variety of current software programs.
Extensive internet use combined with knowledge of computer hardware and components.

REFERENCES
Provided upon request.