Mona Kohail Email & Phone Number

Laval, Quebec, Canada

-Perform all data review related for PK,Oligo, and ADA groups.-Write production and validation report.-Participate to the identification of continuous process improvement areas, in compliance with GLP processes and documentation for QC activities.-Ensuring that the analytical data generated is on par with regulatory requirements. -Conducting different kinds of calculations that used in the pharmaceutical industry.-Ensuring that all analysis is conducted according to approved… Show more -Perform all data review related for PK,Oligo, and ADA groups.-Write production and validation report.-Participate to the identification of continuous process improvement areas, in compliance with GLP processes and documentation for QC activities.-Ensuring that the analytical data generated is on par with regulatory requirements. -Conducting different kinds of calculations that used in the pharmaceutical industry.-Ensuring that all analysis is conducted according to approved test methods, standard operating procedures.-Checking all the laboratory notebooks for correctness of raw data and verifies all reagents, standards and equipment used are within the acceptable range.-Conducting training to reduce the laboratory documentation errors and providing continuous updates on this to the QC management.-Ensure compliance with all Safety, Health, and Environmental rules, procedures and regulations as it pertains to lab function.-Complete and maintain the required quality records and/or documents as directed by the department standard operating procedures-Trains the new analysts for (GDP) and document corrections and provide guidance accordingly.-Trains and guide the new QC reviewers Show less

Laval, Quebec, Canada

-Participate to the identification of continuous process improvement areas, in compliance with GMP processes and documentation for QC activities.-Ensuring that the analytical data generated is on par with regulatory requirements. -Conducting different kinds of calculations that used in the pharmaceutical industry.-Ensuring that all analysis is conducted according to approved test methods, standard operating procedures.-Checking all the laboratory notebooks for correctness of raw… Show more -Participate to the identification of continuous process improvement areas, in compliance with GMP processes and documentation for QC activities.-Ensuring that the analytical data generated is on par with regulatory requirements. -Conducting different kinds of calculations that used in the pharmaceutical industry.-Ensuring that all analysis is conducted according to approved test methods, standard operating procedures.-Checking all the laboratory notebooks for correctness of raw data and verifies all reagents, standards and equipment used are within the acceptable range.-Conducting training to reduce the laboratory documentation errors and providing continuous updates on this to the QC management.-Ensure compliance with all Safety, Health, and Environmental rules, procedures and regulations as it pertains to lab function.-Complete and maintain the required quality records and/or documents as directed by the department standard operating procedures-Trains the new analysts for (GDP) and document corrections and provide guidance accordingly. Show less

Laval, Quebec, Canada

The Senior Analyst performs assay validation and sample analysis activities for the determination of biomarkers, drug concentrations or immunogenicity assessments using ligand binding assays technologies. Ensures that analyses are performed in accordance with both industry and governmental regulations.

Montreal, Canada Area

The Analyst II is responsible for performing quantitative drug determinations of biological samples using a variety of extraction methods including liquid-liquid extractions, solid phase extractions and protein precipitations. He is also responsible for performing baseline integration. The Analyst ensures that analyses are performed in accordance with both industry and governmental regulations.

Canada - Laval

The Analyst I is responsible for performing quantitative drug determinations of biological samples using a variety of extraction methods including liquid-liquid extractions, solid phase extractions and protein precipitations. The Analyst ensures that analyses are performed in accordance with both industry and governmental regulations.

Montreal, Canada Area

Calibrating analytical instrument.Preparing reagents and buffer solutions.Updating experiments method & the MSDS for lab materials.Performing HPLC (specially Agilent instrument), GC-MS. Validation of pharmaceutical drug.

Dec, Analytical Chemistry

Diploma, Clinical Laboratory Science/Medical Technology/Technologist