Anna di Matteo

Anna Di Matteo has extensive work experience in the pharmaceutical industry. Anna most recently worked as a GMP Compliance Project Manager at PQE Group since September 2022. Prior to that, they were a Complaint & Deviation Team Leader at Corden Pharma from April 2021 to September 2022.

Anna also worked at Sanofi, where they held the role of Pre-Filling Supervisor, Sterile Area from June 2019 to February 2020. Anna was responsible for organizing, managing, and optimizing departmental activities. Anna also handled writing and reviewing SOPs, risk assessment, batch record review, and department training.

Before their role at Sanofi, Anna worked as a Quality Assurance Specialist at Corden Pharma from September 2017 to August 2018. Anna also had short-term positions at Patheon as a PDS Quality on the Floor Specialist in 2017 and at AbbVie as a QA Market Ops Officer from June 2014 to December 2016.

Earlier in their career, Anna worked as a QA Consultant at S4BT - Solutions for Business & Technology, where they were assigned to Novartis Vaccini. Anna gained experience in change request management, deviation handling, and root cause analysis from August 2013 to May 2014.

Anna's career started as a QC Analyst at BSP Pharmaceuticals from April 2013 to August 2013. Anna was involved in writing procedures, updating analytical methods, and handling laboratory deviations.

Prior to BSP Pharmaceuticals, Anna worked as a QC Analyst at Janssen, Pharmaceutical Companies of Johnson & Johnson from July 2010 to March 2013 and at Bristol Mayer Squibb from November 2007 to December 2009. In both roles, they were responsible for writing procedures, handling laboratory deviations, and preparing for regulatory inspections.

Overall, Anna Di Matteo has extensive experience in quality assurance and compliance in the pharmaceutical industry, with a focus on managing deviations, completing risk assessments, and ensuring regulatory compliance.

Anna Di Matteo attended Federico II di Napoli from 1998 to 2007, where they obtained a degree in Biiologo with a field of study in Scienze biologiche e fisiche.

Anna also holds multiple certifications:

- In December 2007, they passed the Esame di Stato di abilitazione all'esercizio della professione di Biologo from Università degli Studi di Napoli Federico II.

- In February 2008, they received training in the use and technology background of BactliFlow ALS from AESCHEMUNEX S A.

- In December 2007, they received training in the use and technology background of CHEMSCAN from AESCHEMUNEX.

- In November 2011, they completed fedegari moist heat sterilizers-Maintenance activities training from Fedegari Group.

- In April 2013, they completed a Corso di formazione sui rischi di Mansione per attività a rischio Alto settore Chimico Farmaceutico from BSP Pharmaceuticals S.p.A.

- In June 2015, they completed Root Cause Analysis Training from Tartari & Partners.

- In September 2019, they obtained a Corso Base GMP certification from Specialty Pharma Education Center.

- In February 2020, they completed Gestione Allarmi, Processo e controllo di processo Thema 3 e Thema 4 training from Fedegari Group.