Pauline Sylvest Salanti

Pauline Sylvest Salanti has a diverse work experience in the field of quality assurance and regulatory compliance. Pauline is currently the Director of QA and Report Management at Scantox since January 2021. Prior to this, they worked as the Head of QA and Associate Director at Charles River Copenhagen from January 2020 to January 2021, managing a team of 5 QA auditors and overseeing the archive with 2 reports. Before that, they served as a Medicines Inspector at Lægemiddelstyrelsen from April 2017 to January 2020. From December 2015 to March 2017, they were a Senior Quality Specialist at LEO Pharma, responsible for pre-clinical activities and monitoring clinical trials outsourced to CROs. Pauline also has experience as the Head of Quality Assurance at Unilabs from April 2015 to November 2015, managing a team and conducting audits. Additionally, they worked as a QA Chemist Research and Development at ALK Abelló in 2014. Pauline started their career at CiToxLAB Scantox in 2002, where they held various roles including Head of Quality Assurance and Archives from January 2006 to April 2014 and QA Auditor from July 2002 to December 2005.

Pauline Sylvest Salanti completed their education at two institutions. From 1992 to 1996, they attended Kolding tekniske skole where they studied Veterinary Nurse. Later, from 2011 to 2013, they pursued an MSc degree in Quality Management in Scientific Research and Development at Cranfield University - Cranfield School of Management.