Groupe PARIMA
Sharon Candoleta has over 17 years of experience in the quality assurance and validation field. Sharon began their career in 2003 as a QA Computer Validation Auditor at Charles River Laboratories. In 2006, they joined Pharmascience as a Process Validation Specialist and a Computer Systems Validation Specialist. In 2012, Sharon moved to TouchTunes Interactive Networks as a Software Quality Control Project Coordinator. Sharon then worked at JUBILANT HOLLISTERSTIER GP as a Senior Validation Specialist in 2013. In the same year, Sharon took on a role as Quality Assurance (QA) Analyst, Point of Sales & Store Solutions at Dollarama. From 2016 to 2019, they worked at SNC-Lavalin as a Computer Systems Validation Specialist. In 2020, Sharon joined Groupe PARIMA as a Senior Project Manager for Computer Systems Validation, where they developed an IT Computerized Systems Validation Program, provided CSV guidance for system implementations, and developed and revised SOPs for multiple GxP systems and IT operations.
Sharon Candoleta completed a Bachelor of Science in Biology from Concordia University, an A.E.C in Programmer Analyst from Herzing College, and a D.E.C in Social Sciences from Vanier College.
Groupe PARIMA
2 followers
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