Pino Cabrera Cabrera
Consulting Manager at Qualipharma
Based in Madrid, Spain
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Seniority
Manager
Department
General Business & Management
Location
Madrid
Industry
Pharmaceutical Manufacturing
Company size
162
Contact information
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p•••••••@qualipharmagroup.com
Phone
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Background
About Pino Cabrera Cabrera
Pharmacist with a Master’s in Pharmaceutical and Parapharmaceutical Industry (CESIF) and MBA. Currently a Consultant, GMP Auditor, and Trainer at QUALIPHARMA, with expertise in process and cleaning validation, risk analysis, and GMP compliance. Previous experience includes- 2 years as Validation Specialist at FAMAR HCS, handling process validation, cleaning validation, and operational qualification for solid and sterile manufacturing- 7 years in Operational Quality Assurance, focusing on batch release, deviation investigations, and GMP compliance in diverse production environments. Fluent in English and German, with intermediate French. Skilled in Navision and Microsoft Office. Passionate about ensuring quality and compliance in pharmaceutical manufacturing.
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