Experience

Medicom Group

• Canada
• Medical Equipment Manufacturing
• 200 - 300 Employee

• Quality Assurance Specialist

  • Nov 2021 - Present



Groupe PARIMA

• Canada
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Quality Assurance Specialist- Operations

  • Sep 2020 - Nov 2021



Laboratoires Confab Laboratories

• Canada
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• CAPA Specialist

  • Jan 2020 - Sep 2020



Prometic Bioproduction Inc.

• Canada
• Biotechnology Research
• 1 - 100 Employee

• Quality Assurance Specialist

  • Jan 2019 - Dec 2019



ARA - Avanti Rx Analytics Inc

• Canada
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Quality Assurance Specialist

  • Sep 2017 - Jan 2019



Canadian Analytical Laboratories

• Canada
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• QA Document Reviewer

  • Mar 2017 - Aug 2017



Laboratoires Confab Laboratories

• Canada
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Analytical Service Auditor

  • Nov 2015 - Feb 2017



UQAM | Université du Québec à Montréal

• Canada
• Higher Education
• 700 & Above Employee

• Research assistant in the laboratory of Pr. Steve Bourgault (intern)

  • Sep 2015 - Nov 2015

  • Synthesize different kind of peptide by automatic synthesizer (Tribute UV / IR). • Perform chemical cleavage to remove the resin of the peptide. • Perform the lyophilization step to recover the crude peptide. • Conduct mass spectroscopy (TOF-MS) to obtain the molar mass of the peptide. • Purify the crude peptide by preparative and analytical HPLC • Synthesize different kind of peptide by automatic synthesizer (Tribute UV / IR). • Perform chemical cleavage to remove the resin of the peptide. • Perform the lyophilization step to recover the crude peptide. • Conduct mass spectroscopy (TOF-MS) to obtain the molar mass of the peptide. • Purify the crude peptide by preparative and analytical HPLC



samisaz pharmaceutical company

• Quality assurance specialist

  • Sep 2009 - Nov 2012

  • Inspected and assessed the production lines to ensure that equipment, materials and production processes are in accordance with the principles of good manufacturing practices(GMP), regulations and standards.• Performed physical analyses on the granules, the basic tablets, film coated tablets and enteric coated tablets on USP and BP pharmacopoeias.• Examine the packaging and labeling of products according to regulations.• Control all stages of drug production.

• Laboratory Analyst

  • Sep 2007 - Aug 2009

  JOB RESPONSIBILITIES:• Performed complex sample preparations and executed the analyses by classical and instrumental test methods; following the standard operation procedures (SOPs).• Performed chemical analyses on finished products, process validation and new products for R & D department.• Documented the results according to WHO methods and based on pharmacopoeia, USP & BP.• Generated, revised and approved the SOPs and procedures related to quality systems and GLP, oversaw the distribution of new issues and the removal of obsolete SOPs from circulation.• Performed activities related to development, qualification and validation of analytical methods.• Supervise other analysts, technicians and technologists. Show less