Angelika Athey

** ******** *****

Pittsgrove, NJ 08318

856-***-****

E-mail: adwreq@r.postjobfree.com

Overview

I am a highly motivated individual with an excellent educational background and work history. I am a resourceful and solution-oriented professional with strong organizational and interpersonal skills. Areas of expertise including, but not limited to, the following:

HPLC Analysis; Method Development and Validation

GC, GC/MS and GC-Headspace experience

TOC Analysis

Extensive Wet Chemistry

SOP & cGMP Documentation

Microbiology

Karl Fischer

UV-Vis

FT-IR

Optical (Specific) Rotation

Product Stability

Administrative Duties

R&D/QC Support

Electron Microscope

Responsible for CDS and DEA licensing requirements

Various Computer Skills including Microsoft Word and Excel; LIMS

Participated in a collaborative study with FDA on Apple Juice Concentrates (published)

Former member of the Fruit Juice Adulteration Committee

Education & Training

EAS Short Course, GC Applications Atlantic City, NJ

EAS Short Course, Atlantic City, NJ

Method Development and Validation Training

HPLC & VP Software Training

Shimadzu Columbia, MD

LC Resources, Saddlebrook, NJ

Advanced HPLC Training

LC Resources, Saddlebrook, NJ

HPLC Method Development Training

Rider University, Lawrenceville, NJ

Major: Bachelor of Arts Biology; Minor: Psychology

Work History

Teligent Pharma, Buena, NJ

Duties include analysis of actives in finished veterinarian pharmaceuticals and cosmetic & consumer products, stability testing of finished products, method development for HPLC and GC of actives in new products using USP, BP and ICH guidelines, validation of these methods and documentation of research using current FDA regulations. Process validation of bulk cosmetic products produced and also cleaning validation for the production of these products. Other duties include the microbiological assay of raw materials and finished cosmetic products. Other responsibilities include ordering supplies and chemicals for R&D, QC and Production. Duties also include the writing of SOPs and cGMPs.

Siegfried, USA

3rd shift supervisor/ analytical chemist for API products, following cGMP guidelines of the FDA, EPA and DEA. Duties include, but not limited to, LC, GC, GC-Headspace (Totalchrom), NAT, UV, Optical Rotation and various wet chemistry analyses of finished and intermediate drug products, both controlled and non-controlled. Responsible for review and release of analyses to production for further processing.

IGI, Inc., Buena, NJ

Duties include analysis of actives in finished veterinarian pharmaceuticals and cosmetic & consumer products, stability testing of finished products, method development for HPLC and GC of actives in new products using USP, BP and ICH guidelines, validation of these methods and documentation of research using current FDA regulations. Process validation of bulk cosmetic products produced and also cleaning validation for the production of these products. Other duties include the microbiological assay of raw materials and finished cosmetic products. Other responsibilities include ordering supplies and chemicals for R&D, QC and Production. Duties also include the writing of SOPs and cGMPs.

Clement Pappas, Inc., Seabrook, NJ

Duties included HPLC analysis of raw ingredients and finished products in the fruit juice industry, GC and GC/MS analysis of pesticides; microbiological testing of production equipment, and bench chemistry analysis of preservatives; responsible for acquiring state licensing with NJDEP for water and wastewater analysis and annual blind sample analyses to maintain certification. Testing included COD, BOD, Grease and Oil, pH, TSS, etc.

Seabrook Bros. & Sons, Inc., Seabrook, NJ

Duties included microbiological testing of frozen fruits and vegetables.

Vineland Laboratories, Vineland, NJ

Duties included the manufacturing and QC analysis of poultry vaccines.

References and Supporting Documents Furnished Upon Request

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