Groupe PARIMA
Nancy Austin has a diverse work experience in the pharmaceutical industry. Nancy began their career as a Regulatory Affairs and Compliance professional at IntelGenx Corp from March 2006 to December 2011. Following this, they worked as an R&D Chemist at Delta Pharma Inc. from June 2013 to December 2015. Nancy then joined Pharmetics Inc. as an R&D Manager and Technical Support from January 2016 to April 2018. Nancy is currently working as a Project Manager at Groupe PARIMA Inc since April 2018.
Nancy Austin has a strong educational background in chemistry. Nancy obtained their Master of Science (M.Sc.) degree from Concordia University, specializing in Biophysical Chemistry and Surface Chemistry. Nancy pursued their studies at Concordia University from 1999 to 2005, and during this period, they completed their M.Sc. degree in Chemistry. Additionally, they also completed their Master of Science (M.Sc.) degree in the same field of Biophysical Chemistry and Surface Chemistry from Concordia University. This degree program lasted from 2003 to 2005.
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