Pierre Landry has a long and varied work history. Pierre began their career in 1981 as a Laboratory Technician at McGill University. In 1982 they moved to Schering as a Packaging Component Inspector, where they reviewed procedures for the inspection of packaging items and introduced levels of classification of defects. In 1989 they joined DRAXIS Pharma Inc as a QA Specialist and CAPA specialist, and also acted as a product complaint investigator. Pierre also collaborated with the implementation of the SAP System (ERP/3). In 2008 they moved to WINPAK Heat Seal Packaging Inc as Manager, Compliance and Regulatory Affairs. Finally, in 2011 they joined Groupe PARIMA Inc as a QA Specialist.
Pierre Landry attended Laval Catholic High School from 1972 to 1977, where they obtained their High School Certificate. Pierre then went on to attend Dawson College, where they received their Chemical Technology Diploma (D.E.C) in 1981. In 1990, they enrolled at HEC Montréal, where they obtained their BsC. in Gestion des opérations, informatique, qualité in 1999.
Groupe PARIMA
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Groupe PARIMA is a Contract Development and Manufacturing Organization (CDMO), established in 1994. We have developed an expertise in the development and manufacturing of non-sterile liquids, suspensions, and semi-solid drug products. This strategic focus has allowed us to establish a unique expertise to support your product development and manufacturing needs, which, combined to our operational flexibility and commitment to delivering on time, enables us to operate as an extension of your team. Over the years, we have added specialized capabilities such as handling of low-flash point mixtures, and packaging metered-dose sprays (nasal or sublingual), towelettes and sachet/stick/packs. Our business is 100% free-for-service and exclusively focused on contract services. We are here to help you meet your company objectives, not to compete with you. We have been favorably inspected by the European, US, Turkish and Canadian health authorities, and we are manufacturing products for markets in over 30 countries. Product Development: Formulation Development, Packaging Development, QbD, Process Scale-up, process validation, project management Analytical Testing: IVRT, HPLC, UPLC, LCMS, Particle Size, Microbiology, Viscosity Commercial manufacturing for USA, Europe, Canada Turkey, South America, Mexico, Australia, New Zealand, MENA; Serialization, cold-chain Manufacturing: creams, ointments, lotions, gels, solutions, liquids, suspensions, flammable products (Antiseptic gel), inert atmosphere Packaging: Bottles, Jars, Sprays, Pumps, Tubes, Airless Pumps Pledgets/towelettes, Nasal Sprays, Sublingual Sprays, Metered-dose delivery, Syringe applicator (non-sterile), sachets and Stick packs, inert atmosphere