Camillo Bologna
Quality Unit Director and Qualified Person at Mipharm S.p.A.- Claim this Profile
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Italiano Native or bilingual proficiency
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Inglese Full professional proficiency
Topline Score
Bio
Credentials
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Qualified Person
AIFA Agenzia Italiana del farmacoMay, 2013- Nov, 2024 -
State License as Pharmacist
Università degli Studi di Pavia
Experience
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MIPHARM SPA
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Italy
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Pharmaceutical Manufacturing
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100 - 200 Employee
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Quality Unit Director and Qualified Person
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Nov 2019 - Present
Quality Unit Director in charge of Quality Assurance, Quality Control and Regulatory Departments.
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Qualified Person
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Dec 2016 - Present
Qualified Person of the site responsible for supervising and managing the Quality System of the site.In charge of Quality Assurance and Regulatory Departments.Mipharm is an italian pharmaceutical company, founded in 1998, as the result of a spin-off from Novartis Farma spa. Mipharm is a centre of excellence in Italy for third party manufacturing, new products development and special services. The productions carried out in Mipharm include: several solid forms (capsules, tablets, granules), liquids for internal use, suppositories, semisolids, medical devices and cosmetics. Show less
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Bayer
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Chemical Manufacturing
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700 & Above Employee
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Validation Head and Qualified Person
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2011 - Nov 2016
Head of Validation department at Bayer HealthCare Manufacturing Segrate site. The activities of the function are mainly: manufacturing and cleaning process validation, coordination of Investigational Medicinal Products manufacturing, technology transfer and life cycle management activities, product and process development, investigation activities on production issues / deviations. Since 2013 I've been also Qualified Person of the site. Head of Validation department at Bayer HealthCare Manufacturing Segrate site. The activities of the function are mainly: manufacturing and cleaning process validation, coordination of Investigational Medicinal Products manufacturing, technology transfer and life cycle management activities, product and process development, investigation activities on production issues / deviations. Since 2013 I've been also Qualified Person of the site.
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Bausch + Lomb
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United States
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Pharmaceutical Manufacturing
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700 & Above Employee
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Quality System Officer
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2009 - 2011
Quality System Officer in Quality Assurance department: responsibility for change management coordination, Product Quality Review redaction, Corrective and Preventive Actions handling, Batch Record Review. Quality System Officer in Quality Assurance department: responsibility for change management coordination, Product Quality Review redaction, Corrective and Preventive Actions handling, Batch Record Review.
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Intendis
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Pharmaceutical Manufacturing
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1 - 100 Employee
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Laboratory analyst
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2008 - 2009
Analyst at Pharmaceutical Development laboratory partecipating in the following activities: life cycle management, manufacturing and analysis of trial batches at lab-pilot scale, investigation activities on production issues / deviations, manufacturing process development and validation activities. Analyst at Pharmaceutical Development laboratory partecipating in the following activities: life cycle management, manufacturing and analysis of trial batches at lab-pilot scale, investigation activities on production issues / deviations, manufacturing process development and validation activities.
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Education
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Università degli Studi di Pavia
Medicinal Chemistry and Pharmaceutical Technology -
Liceo Classico A. Manzoni
Diploma di maturità Classica
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