PBE Expert Inc

Our Experts



Vice President

Jean Bédard



Jean Bédard, MBA, is the Vice President for PBE Expert. He has more than 20 years of experience in developing and managing companies in the highly-regulated life science sector.

He was Global Vice President Sales, Cold Chain Packaging at Mesa Labs, Vice President Operations at Mesa Canada, President and CEO of Infitrak, Vice President at Alternatives Technology Pharma and Vice president at Validapro/Pharma Concept. In addition to Mr. Bédard’s extensive work experience, he also holds an MBA in Bio-industries Management, and has had extensive training in management, regulatory compliance, validation and regulatory engineering.


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Vice-president – Cannabis Expert

Paul Laurent



Paul Laurent was born in Montreal, where he completed his primary, secondary and university studies. He has worked for several sectors of activity for the Canadian Government, Hydro-Quebec, universities and the Government of Quebec. Since the 1980s, he has invented commercially successful products and built his own business. Today, he advises inventors and entrepreneurs in product and business development.


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Engineering & cGMP Compliance Director

Azis Shraibi



Dr. Azis Shraibi, Eng, has over 25 years of experience in process engineering, layouts, clean systems and utilities, cleanrooms and Validation in various sectors: pharmaceutical, biotechnology, morphine/cannabis, medical devices, natural health products, cosmetics, nutraceuticals, food, pulp & paper, biorefinery & bioethanol. He is an expert referent for Health Canada & MAPAQ, for the implementation of quality systems, but also for facility compliance audits, in accordance with regulatory requirements: GMP/CGMP, HACCP, ISO-22000, SQF, GFSI.


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Director Engineering and Validation

François Goupil



Process and chemical engineer with a Bachelor from University Laval in Quebec City.
Mr Goupil has more than 15 years experience in engineering, automation, validation of manufacturing equipments, clean utilities, pharmaceutical systems and computer systems CSV (cGMP, GAMP5, CFR-21 part 210, 211, 11).


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Validation & GMP Compliance Director

Marco Charron



Marco Charron Consult, Senior. Validation & Compliance Specialist according to cGMP regulatory requirements of Health Canada, EMA and US FDA :

  • Protocols (QIOQ/PQ) development, tests execution, analysis and report writing;
  •  URS, FDS writing;
  • Factory Acceptance Test (FAT) and Site Acceptance Test (SAT) development;
  •  Validation Master Plan development;Environmental program development and implantation;
  • SOP’s writing;
  • Validation project coordonator and management;
  • Technical advisor for all critical systems and clean utilities
  • Environmental control and cleanroom assessment implementation (ISO14644);
  • cGMP Technical support regarding to FDA and EMEA regulatory compliance.

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QPIC, Tech Transfer, QA, IOQ, Director

Marie-Eve Lestage



Process and chemical engineer with a Bachelor degree from Sherbrooke University and Master level courses in Engineering, concentration in International project management and global engineering. Mrs Lestage has more than 15 years experience in engineering, QPIC, research and development, batch release, SOPprocesses & cleaning validation, validation of cleaning and processesLean manufacturing & Green Belt & technical transfers (cGMP, CFR-21 part 210).


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Our Offices

CANADA

For commercial information, partnership and marketing requests with PBE Expert Inc, please contact :
+1 (514) 616-2692

+ 1 (450) 600-0790 x 253

pbe@pbe-expert.com

pbe@pharmabioeng.com3210, Francis Hughes Street, Laval, QC H7L 5A7

Our International Offices in :

Morocco


+(212) 661142327+ 212 522343291www.kimia.maa.elbahraoui@kimia.co.maRésidence EL HADIKA, 4E étage N°88 Ain Sebaa,Casablanca

Algeria


+213 (0) 5-40-96-12-34+ 213 (0) 31-76-61-83tm.ferlab@gmail.comcontact.ferlab@gmail.com147 bloc C, Ben Zakri, les Terrases, Constantine Algérie

Tunisia


+(216) 96-751-330

pbe@pbe-expert.com

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