Lab Technician

OLEG BORODIN

*** ******* ******, ********, *******, L6R-2G8

Tel: 905-***-****, E-mail:*********@*******.***

Lab Technician

• More than five years of experience in QC Laboratory

• Obtain samples from in-process and packaging lines for inspection and testing

• Generate reports for QA/QC compliance

• Notify management of issues in a timely manner

Perform tests on raw materials, packaging components, in process, stability, finished products

• Performs the following tests: Assay/CU/RC/Dissolution, melting point, pH determination, specific gravity, heavy metals, visual appearance, loss on drying, moisture determination and conductivity.

• Operates and maintains laboratory equipment such as:

HPLC/GC, FT-IR, UV-Visible, Refractometer, Polarimeter and Karl Fisher

• Following SOP,GMP,GLP,GDP,USP,EP requirements and procedures, Process Validation and Stability Protocols

• Compile records and interpret experimental.

• Demonstrates excellent problem solving and multitasking capabilities.

• Excellent knowledge of Empower, Chemstation, Microsoft Word / Excel.

PROFESSOINAL EXPERIENCE

Alphora Research Inc 2009

QC Chemist

Provided support to GMP operations by testing of Raw Materials, In Process controls, Intermediate and Finished products.

• Worked in accordance with established SOP, GMP and safety requirements.

• Carried out assay, purity analysis by HPLC and GC.

• Performed moisture determination by Karl Fisher (KF) and KFCT.

• Used wet chemistry for assay test.

• Preformed Description and ID tests according SOP and USP

• Determined optical activity (amount rotation) by Polarimeter.

• Carried out analysis of products and reactions liaise RD Department.

Achievements: after resourced chemical information suggestion was to make changes for the analytical procedure. CCF (change control form) was initiated and quality of the test was improved.

OLEG BORODIN

104 Seaside Circle, Brampton, Ontario, L6R-2G8

Tel: 905-***-****, E-mail:*********@*******.***

Ciba Vision Sterile Manufacturing, 2007- 2009

QC Associate

Provided analytical support for Sterile Manufactory. Reviewed analytical records and performed internal audit.

• Performed Assay tests by UV-Visible spectrometry and wet chemistry (potentiometric and manual titration) for raw materials, in-process and finished products.

• Determined melting point, specific gravity, pH of the raw materials.

• Performed tests as such: Assay, semi quantitative tests for heavy metals, chloride ions, iron and other ions, limit of non-volatile residue, limit of preservatives, acidity determination for raw materials by physical and chemical method of analysis.

• Reviewed analytical records for in-process and finished products.

Achievements: made recommendation to update SOP and corrected calculation formula. Created discrepancy report after participating in internal audit.

Pancap Inc. 2007 – 2007

QC Chemist

Responsible for the testing, sampling; monitoring of environmental conditions and reviewing of Analytical Data.

• Performed Physical and Chemical tests.

• Performed Assay and ID tests by UV and IR spectrophotometer.

• Carried out determination of water content by KF titration method.

• Operated and calibrated the analytical equipment.

• Reported analytical data and results.

Achievements: validated and calibrated refrigerators which were attended to be used to keep the retained samples.

Genpharm Inc., 2005- 2006

QC Associate

Contributed to R&D product development and the regulatory submission process by conducting routine formulation and process testing validation.

• Performed Dissolution, Assay/ CU tests for hard shell gelatine capsules, sustain and immediate release tablets by HPLC and UV/Visible spectrometry.

• Carried out Identification test by HPLC and UV.

• Recorded data and prepared reports in LIMS.

Achievements: timely completion of the RD projects to meet validation deadline.

OLEG BORODIN

104 Seaside Circle, Brampton, Ontario, L6R-2G8

Tel: 905-***-****, E-mail:*********@*******.***

Patheon Inc., 2004- 2005

Lab Analyst

Performed routine samples testing following GLP/GMP/SOP regulations .

• Carried out Assay/CU/Dissolution/RC tests for solid dosage form (tablets, capsules) by UV, HPLC/GC and Potentiometric titration.

• Performed ID tests by TLC, FT-IR and HPLC.

• Performed physical tests for solid dosage form: weight variation, thickness, hardness, friability and disintegration.

• Carried out determination of residual solvent for solid dosage form by GC (FID).

• Performed loss on drying test.

Achievements: ability to manage multiple projects to satisfy customer needs.

Philip Analytical services 2001- 2004

Laboratory Analyst

Carried out extraction for soil and water samples accordingly SOP and Provincial Regulations .

• Performed extraction of TEH (Total Extractable Hydrocarbons), TP (Total Purgeable) for soil and water samples.

• Analyzed samples by GC chromatography.

EDUCATION:

B.Sc. in Chemistry, degree assessed by University of Toronto, Comparative Ed. Services.

Seneca College Industrial Pharmaceutical Technology certificate program:

• Pharmaceutical Manufacturing Methods

• Clinical Pharmacology and Toxicology

• Industrial Drug Legislation

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