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Pharmaceutical consultant

Érika Rosa Jarzinski

650
51
7
Pharmaceutical consultantGewünschte Stelle
Mo - FrVerfuegbare Arbeitstage

Berufliche Zusammenfassung

Graduation in Pharmacy with Habilitation in Industrial Pharmacy from Universidade Estadual de Londrina (2005). Scientific initiation works with CNPq scholarship for the projects entitled: Immobilization of Bovine Albumin in Vegetable Bush subjected to Previous Treatment with Dimethyl Sulfoxide (2002) and batch culture of Corynebacterium glutamicum MH20-22B for the production of lysine (2003). Work on the characterization of isolated Eugenol (4-Allyl-2-Methoxyphenol) obtained from Syzgium aromaticum (L.) (2003), under other guidance. Acting in the project of monitoring advertising for ANVISA. Course completion project: "Pharmacotechnical Development and Analytical Methodology for Immediate Release and Sustained and Controlled Release Drugs (2005). MBA in Industrial Management from FGV Campinas (2009). Worked in the pharmaceutical industry since 2005; started as an R&D trainee, junior researcher, quality control analyst, and analytical development analyst. Working in major multinational, domestic, and foreign pharmaceutical industries. In 2013 I did an exchange program for English proficiency in the UK. In 2014 I started in the sector of gastronomy and craft beverages as a managing partner for four (04) years; being responsible for development and process management, good quality practices in the area of food, hiring, training, and purchasing team. During this period I took the Empretec course at Sebrae. In 2016 I took an extension course at USP Ribeirão Preto on "Exploration in the nanotechnology sector in Brazil for the pharmaceutical and cosmetic segments: trends and challenges" - FCFRP-USP. I work as an independent consultant in the area of quality, pharmaceutical processes, and regulations since 2018, I developed the quality management system and solve regulatory issues of a correlates distributor that distributes products for neuro and spinal surgeries, a system of which I am responsible until the present moment. I work on projects for the development of the quality system, I guide the development of companies/laboratories for qualification in pharmaceutical equivalence and REBLAS, applying in-company training, applying auditing and applying the regulatory knowledge to prepare them for local health inspection and ANVISA. Since 03/2020 I am a master's student at the School of Pharmaceutical Science of the University of São Paulo - Ribeirão Preto, in the Center for Nanotechnology and Tissue Engineering / Photobiology and Photomedicine Group, with a project in the area of nanotechnology drug development for topical application, using quality by design and big data tools for development and knowledge management.

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