Fabrizia Lo Bosco, PhD
Quality Assurance and Regulatory Affairs Manager at Sanecovit- Claim this Profile
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english Professional working proficiency
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spanish Full professional proficiency
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italian Native or bilingual proficiency
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Bio
Experience
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San.Eco.Vit srl
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Italy
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Personal Care Product Manufacturing
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1 - 100 Employee
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Quality Assurance and Regulatory Affairs Manager
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Apr 2018 - Present
- Manage the documents of the Quality Management System - Internal Auditor for ISO 22716:2008, ISO 9001:2015, IFS-HPC- Evaluate and qualify suppliers of products and services in collaboration with Procurement and R & D departments- Define with the competent company departments the most appropriate solution for non-conformities and customer complaints - Evaluate the need to undertake corrective and / or improvement actions, manage the management process and evaluate its effectiveness- Define and maintain the Internal Audit Program- Carry out the monitoring of the after-sales phase and the documentation of adverse events- Collect data to evaluate the effectiveness of the Quality Management System and its continuous improvement- Draw up and collect all the necessary documents for compliance with the Cosmetics Regulation and related regulations- Notify at ISS dangerous non-cosmetic products and detergency- Notify cosmetic products on the CPNP portal- Check the conformity of the product comparing the certificates of analysis with the reference specifications- Communicate regulatory updates internally to the company- Support the Marketing Department in the development of products formulated by subcontractors, also interfacing with the contractors for the related regulatory aspects- Collecting documentation and preparation of PIF- Verify the conformity of the cosmetic labelling- Deepening and follow the evolution of regulatory issues- Provide the technical and regulatory support required for the Marketing, Quality and R&D functions
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NECOS srl
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Italy
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Personal Care Product Manufacturing
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1 - 100 Employee
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Regulatory Affairs Specialist
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Jun 2017 - Apr 2018
• Collecting documentation and preparation of PIF• Verify the conformity of the cosmetic labelling• Deepening and follow the evolution of regulatory issues• Provide the technical and regulatory support required for the Marketing, Quality and R&D functions• Preparation of documentation, necessary to ensure that systems and regulatory processes are in compliance withnational and international regulatory standards• Support dedicated to each customer questions on the regulatory framework according to pre-established service level(documents, raw material specifications, technical questionnaires and quality)
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Chromavis Fareva
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Italy
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Personal Care Product Manufacturing
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500 - 600 Employee
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Quality Control
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Feb 2017 - May 2017
• Preparation of documentation, necessary to ensure that systems and quality processes are in compliance with national and international regulatory standards• Management of corporate instrumentation according to the company's quality system• Gather and maintain data for production batches ensuring GMP and customer compliance• Support dedicated to each customer questions on the regulatory framework according to pre-established service level (documents, raw material specifications, technical questionnaires and quality);• Support to the sales department on quality demands from customers.
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Regulatory Affairs Specialist
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Oct 2016 - Jan 2017
• Preparation of documentation, necessary to ensure that systems and regulatory processes are in compliance with national and international regulatory standards;• Support dedicated to each customer questions on the regulatory framework according to pre-established service level (documents, raw material specifications, technical questionnaires and quality);• Support to the sales department on quality and regulatory demands from customers.• Collecting documentation and preparation of PIF.
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Itinerari Cosmetici 2016
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Mar 2016 - Jul 2016
R&D Team Leader: Person in Charge of Product an Pack development R&D Team Leader: Person in Charge of Product an Pack development
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Consiglio Nazionale delle Ricerche
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Italy
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Research Services
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700 & Above Employee
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Research grant
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Sep 2013 - Apr 2015
• Study of the volatile components in the shelf life of shellfish by means of gas chromatography and electronic nose in the project De.Cro.Med. entitled "Catch of the Mediterranean: Quality certification and enhancement of shellfish defrosted" (PO.FESR 2007-2013 Action Line 4.1.1.1).
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Stage
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Mar 2013 - Mar 2014
Study and extraction of bioactive components of food matrices
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Education
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Universitat Politècnica de València (UPV)
Doctor of Philosophy (Ph.D.), Mediterrean Fruit Crops -
Università degli Studi di Milano
Course in Cosmetics Science -
Università degli Studi di Palermo
Master's degree, pharmaceutical chemistry and technologies -
Liceo Scientifico
High School Diploma, 98/100