Sara B. possesses extensive experience in quality control and analytical chemistry, currently serving as a Quality Control Data Reviewer at Groupe PARIMA since August 2022. Responsibilities include reviewing documentation and analyzing results in chemistry and microbiology, and validating analytical methods. Previous roles include Immunology QC Data Reviewer at Charles River Laboratories and Analyst positions at Pharmascience and Altasciences, where Sara contributed to liquid-liquid extraction and bioanalytical analyses. A strong educational background includes a Master’s degree in Molecular Medicine and Biochemistry from Université de Montréal and a Master's degree in Microbiology from Université Azad. Sara has also worked as a research assistant, providing expertise in protein production and characterization, alongside consulting experience in microbiology across various industries.
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