Alvaro Calvo has extensive experience in quality control and regulatory compliance within the pharmaceutical industry, currently serving as a Quality Assurance Specialist at Laboratorios Rubió since January 2017. Key responsibilities include managing PQRs, change controls, and product releases, as well as conducting audits and validations. Prior to this role, Alvaro held various positions at Laboratorios Rubió from 2005 to January 2017, including leadership in analytical development projects audited by the FDA. Alvaro's career also includes a role at UQUIFA as a QA Technician, focusing on release processes and compliance. Alvaro holds a Master's degree from CESIF and a Bachelor's degree in Pharmacy from the Universitat de Barcelona, with over 10 years of experience working with GMP regulations.
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