Auro Carlotto Email & Phone Number | More than 10 years’ experience in pharmaceutical companies, QA, Packaging and Production. 3 years’ experience like production and packaging manager in pharmaceutical companies. More than 3 years’ experience in IT. 3 years’ experience with SOP’s document creation a GxP document revision. Experience with CAPA’s, Changes 1 year like project manager in decommissioning in international companies. 1 year like expert IT support in decommissioning and disentanglement activities. Expert team leader. Ability to work like a team member. Trilingual: Italian, Spanish, English. Expert in IQ, OQ, PQ, of QC systems, pharmaceutical products, and packaging/production equipment. Expert in risk prevention. Expert in problem solving. Expert in QC laboratory, production, and packaging GMP systems. Experience with specific legal and regulatory requirements in the long-term archive in the pharmaceutical industry.

Auro Carlotto

More than 10 years’ experience in pharmaceutical companies, QA, Packaging and Production. 3 years’ e...
Rincón De La Victoria, Rincón De La Victoria, Spain

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Auro Carlotto’s Email acarlotto@airzoneitalia.it

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Auro Carlotto’s Location Rincón De La Victoria, Rincón De La Victoria, Spain

Auro Carlotto’s Current Industry Airzone Italia By Altra

Auro Carlotto’s Prior Industry Msd | Merck Sharp And Dohme | Schering Pharmaceuticals

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Work Experience

Airzone Italia By Altra

Project Engineer

2022-03-01 00:00:00 - Present

Msd

It Coordinator For Decommissioning And Disentanglement Activities

2016-01-01 00:00:00 - 2022-06-01 00:00:00

Merck Sharp And Dohme

Manufacturing & Packaging Leader

2012-03-01 00:00:00 - 2012-10-01 00:00:00

Schering Pharmaceuticals

Manufacturing Support

2005-10-01 00:00:00 - 2012-03-01 00:00:00

Skills

No Skills Available

Languages

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FAQ About Auro Carlotto

Auro Carlotto is located at
Rincón De La Victoria, Rincón De La Victoria, Spain

Auro Carlotto is a More than 10 years’ experience in pharmaceutical companies, QA, Packaging and Production. 3 years’ experience like production and packaging manager in pharmaceutical companies. More than 3 years’ experience in IT. 3 years’ experience with SOP’s document creation a GxP document revision. Experience with CAPA’s, Changes 1 year like project manager in decommissioning in international companies. 1 year like expert IT support in decommissioning and disentanglement activities. Expert team leader. Ability to work like a team member. Trilingual: Italian, Spanish, English. Expert in IQ, OQ, PQ, of QC systems, pharmaceutical products, and packaging/production equipment. Expert in risk prevention. Expert in problem solving. Expert in QC laboratory, production, and packaging GMP systems. Experience with specific legal and regulatory requirements in the long-term archive in the pharmaceutical industry.