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The sample below is for a Quality Assurance Audit Resume Sample. This resume was written by a ResumeMyCareer professional resume writer, and demonstrates how a resume for a Quality Assurance Audit Resume Sample should properly be created. Our Certified Professional Resume Writers can assist you in creating a professional document for the job or industry of your choice. A professional resume writing service can significantly increase your changes of securing employment in a quick time manner.

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Results focused and detail oriented professional with extensive experience in carrying out quality control programs and methods into place to ensure production of goods comply with industry regulations. Analytical, and a logical thinker, highly reliable in interpreting standard policies and procedures and conducting routine testing of finished products, in process, validation, and stability samples. Highly efficient at researching, data extraction and report making, with strong ability to study, analyze and detect errors. A proven leader and an excellent communicator recognized for ability to establish and maintain effective working relationships across cross-functional teams and diverse individuals at any levels.

Core Competencies
Project Management & Coordination • Quality Control/Assurance Audits & Reviews • Process Evaluation
• Needs Assessment • Documentation • Reports Development • Risk Management • Training Delivery


Catalent Pharma Solutions, Somerset, NJ 10/2004 – Present
Scientist, Analytical Services
Perform laboratory investigations for aberrant/atypical and OOS results. Carry out method validation, evaluation, and development, optimization for dissolution, assay, and related substances methods.
• Conduct tests on stability samples, release samples, and formulation R&D samples.
• Manage data review of laboratory notebooks and validation or summary reports.
• Develop method validation reports as well as laboratory investigation reports.

Alpharma, Elizabeth, NJ 05/2002 – 10/2004
Chemist, Quality Control
Oversaw routine testing of finished products, in process, validation, and stability samples. Managed various tests including assay, content uniformity, related compounds, dissolution, dissolution profile, and identification.
• Assisted QC chemists in using Millennium32 software, and maintained HPLC equipment.
• Updated and maintained documentation on procedures, data, and results in laboratory notebook.
• Provided training to new chemists as necessary.

West-Ward Pharmaceutical, Eatontown, NJ 04/2000 – 05/2002
Chemist, Quality Control
Conducted tests on process validation samples. Performed assay, content uniformity, dissolution, related compounds, identification tests on finished products, in process, and stability samples. Documented tests in laboratory notebook.
• Maintained and calibrated HPLC components and dissolution apparatus.
• Facilitated training for new chemists in laboratory techniques and instrumentation.


Bachelor of Science in Chemical Engineering, 05/1999
Rutgers University – Newark, NJ

Associate of Science in Chemistry, 05/1995
Raritan Valley Community College – Branchburg, NJ

Totalchrom software, Millennium32 software, TrackWise software
HPLC, GC, UV/VIS, FT-IR, TLC, IC, dissolution apparatus
cGMP, USP, ICH Guidelines

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