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Quality Control Data

Location:
Princeton, NJ
Salary:
65000
Posted:
June 24, 2015

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Resume:

acqefr@r.postjobfree.com

609-***-****

** ******* ***** ***** **, 08638

ROBERT EZEUKA

SUMMARY

Associate Scientist / Quality Control Analyst with 5+ years experience (4+ years industrial) in Analytical Chemistry within the pharmaceutical industry. Comprehensive knowledge with analytical instrumentation including: HPLC (Chemstation Software) with RID, UV-Vis, crystallography, and MS detectors. Extensive experience in sample analysis, aseptic technique, gram staining and other microbiology techniques. Proficient in analyzing and interpreting biological, chemical, and microbiological data using exceptional quantitative skills, critical-thinking, and mathematical skills. Proficient in analyzing and interpreting biological, chemical, and microbiological data using exceptional quantitative skills, critical-thinking, and mathematical skills. Superb communication, interpersonal, leadership, and problem-solving skills with the ability to excel in challenging and deadline-driven environments and ensure that projects are completed on time and within budget.

Highlights

Equipment calibration

Reporting

Regulatory compliance

Operational Improvements

Raw material spefication

Program implementation

Laboratory analysis

Docimentation

EXPERIENCE

Bristol-Myers Squib New Brunswick, NJ

Associate Scientist / Quality Control Analyst December 2010- Present

Perform troubleshooting in compounding/manufacturing for adjusting the batches to meet the product specifications.

Familiarity and demonstrated competency, after training, with test equipment including gas chromatography (GC), high performance liquid chromatography (HPLC), spectrometers, fluorimeters, polarimeters, dissolution testers, volumetric and gravimetric analyzers, balances,

Performs adjustments minor repairs as needed to instruments and equipment as indicated by Instrument Operating Procedures

Extensive knowledge of structure solution from single-crystal and powder data. Including structure solution, qualitative and quantitative analysis, polymorph identification and elucidation

Experience consultant in good laboratory practices (GLP), pharmaceuticals, process analytical control and nano-materials

Responsible for daily quality checks on each phase of the manufacturing process.

Performed functional testing of raw materials including HIV, HCV, HBV, CT/NG, MTB, MAV, CMV, and blood screening products..

Experienced crystallographer and X-ray powder diffractionist. Responsible for the maintenance and use of three Bruker SMART1000 CCD single-crystal diffractometers, D5 X-ray powder diffractometers, a Bruker D8 GADDS powder/single-crystal diffractometer and two Bruker Small Angle X-ray Scattering instruments

Maintains laboratory notebook, records raw data, calculates results, and reports results to laboratory supervisor and or computer database.

Prepare the batches of formulas for submitting the samples to marketing and reformulating them based upon feedback.

Maintained and updated test data and documented laboratory activities using the LIMS system.

Aid senior scientists in developing PK and ADA assays and prepare/label conjugates.

Comfortable with developing comprehensive graphs and charts from complex data

Experience in manufacturing design

Large equipment maintenance and quality control

Versatile as well as flexible

Can work on large or small job sites

LABORATORY SKILLS/EQUIPMENT

Powder X-ray diffraction.

Kikusui Tablet Press

Thomas Engineering Accela-Cota FLEX 500 Batch Tablet Coater

Quadro Comil underdriven and overdriven

Thermogravimetric Analysis

PH 300 Korsch Tablet Press

High Pressure Liquid Chromatography

Knowledge of statistics for experimental design, data analysis, and quality control

General Area Detector Diffraction System (GADDS)

Knowledge of performing stability testing using pH meter, Viscometer, Sonicator.

Crystallography (crystal x-rays)

Differential Scanning Calorimetry

Roller Compacter

Spectroscopy, Micro-calorimetry

Understanding of Protein Structure

Years of cGMP experience

GLP//GMP Lab Procedures * Team Leadership/Management

FDA Regulations

SOP Development

Study Sample Analysis

COMPUTER

Computer Skills: MS Windows, Microsoft Office, Microsoft Excel, LIMS, Watson, MS Word, Microsoft Suite, PRISM/CARA, Ariba, Softmax 4.8 and Adobe Photoshop

Trackwise, Documentum, QIS, and DCN

Awards and Accomplishments: STAR award 2012 to basically employ hard-work and outstanding performance

Responsibilities:

I took the responsibility of preparing solutions, compounds, equipment needed for conducting the test by chemists and senior persons in the chemical laboratory. I also took the tasks of analyzing data of chemical compound results given to me and interpreting the results and recording the same. I underwent training in using techniques and equipment in chemical lab from chemists in the department. Apart from this I also assisted the senior chemists and chemists and learned daily small operations and tasks in laboratory.

EDUCATION

Rutgers University

Bachelor’s of Science in Chemistry May 2010

GPA 3.0 (Science courses)

Dean’s List 2 semesters

Rutgers University

Master of Science in Molecular Biology May 2014

GPA 3.15

Dean’s List 1 semester



Contact this candidate