Quality Control Technician

Carol A. Morgan

**** ***** ******, *********, ********** 92509

951-***-****

email: *********@*******.***

Objective:

To obtain a position in pharmaceutical industry or healthcare where I can maximize my skills.

Summary of Qualifications:

. Several years working as an efficient organized biologist in numerous

areas including but not limited to: food inspection, hospital

emergency medical technician, research laboratory technician,

analytical chemistry technician, microbiology technician, clinical

research associate, and investigational drug development in neurology

and oncology research.

. Results-oriented, high-energy, hands-on professional, with a

successful record of accomplishments in the pharmaceutical clinical

research and analytical quality control manufacturing industry.

Experienced accurate and deep knowledge of monitoring of

investigational sites. Detailed knowledge of GCP and ICH guidelines

including understanding of regulatory requirements. Developing and

providing site training sessions. Clinical statistical analysis to

determine trends. Filing of regulatory documentation. Communicating

with regulatory agencies. Organization and presenting at research

meetings. Managing Clinical Research Organizations.

. Major strengths include strong leadership, excellent communication

skills, competent, strong team player, attention to detail, dutiful

respect for compliance in all regulated environments, as well as

supervisory skills including, scheduling, training, payroll, and

other administrative tasks. Computer and internet literate.

. Microbial testing: Practical and theoretical knowledge of WHIMIS, the

standard aseptic method, culture inoculation and identification of,

various pathological species and their related vectors. Setup and

accurate analysis of microbes present in food manufacturing inline

testing prior to manufacture, raw material and sample analysis.

Quality control check for FDA and company requirements.

. Chemical testing: Accurate testing of raw materials and in process

samples during manufacturing. Finished product analysis and

certificate of analysis generation.

. Technical Writing: Experience with new drug applications,

institutional review board applications and quarterly reports.

Creating case report forms for drug studies and clinical standard

operating procedures for a start up drug company. Presenting research

results at meetings, primary investigator meetings and to the public.

Professional Accomplishments:

. RN License in good standing with California State Board of Nursing -

2012.

. RN License in good standing with the College of Nurses of Ontario -

2011.

. RN License in good standing with the Arizona State Board of Nursing -

2011.

. Nursing Scholarship Winner University of Ottawa.

. Participated in the expedited approval of over the counter and

prescription drugs in the United States.

. Certificate of Appreciation - IBRD - Rostrum Global.

. Organized and presented at The First Avon Breast Cancer - University

of California, Irvine Symposium.

Work History:

. Quality Control Technician, Golden State Foods, City of Industry, CA:

2004.

. Chemist, Stepan Company, Anaheim, CA: 2003-2004.

. Breast Cancer Coordinator, Chao Family Cancer Center, Orange, CA:

2000.

. Clinical Research Monitor/Manager, NeoTherapeutics, Irvine, CA: 1997-

1999.

. Project Research Associate, IBRD Rostrum Global, Irvine, CA: 1993-

1997.

Education:

. Bachelor of Science Nursing. Cum Laude, University of Ottawa, Ottawa,

Ontario, Canada.

. Bachelor of Science Environmental Biology, McGill University,

Montreal, Quebec, Canada.

Publications:

. J. Appl. Physiol. 61(4)1329-1336:"Respiratory Adaptation to Chronic

Hypoxia in Newborn Rats."

Other:

. French Language.

. American Heart Association BLS for Health Care Professionals

(Current).

. California Drivers License

. Word, Excel, PowerPoint other data spread sheets.

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