Lovleen Sethi

Lovleen Sethi has extensive experience in quality assurance and compliance roles in the biotech and pharmaceutical industries. Lovleen is currently the Director of Quality Systems & Compliance at Kymera Therapeutics. Prior to that, they worked as an Associate Director of Quality Systems at Nuvation Bio, a Senior Quality Assurance Manager at Axovant Gene Therapies, and a Quality Assurance Project Lead/Manager at Purdue Pharma. Lovleen also held roles as a Senior QA Investigations Specialist at Actavis and a Sr. QA Specialist IV, Compliance Project Manager, and Lead Investigator at Wyeth Biotech. Additionally, they have experience as a Senior Cell Therapy Specialist at Progenitor Cell Therapy, where they were responsible for stem cell manipulation, cryopreservation, and investigation of non-conforming products.

Lovleen Sethi completed a PhD in Leadership and Higher Education from Capella University from 2012 to 2016. Prior to that, from 2000 to 2003, they earned an MS in Molecular Biology from Montclair State University. Additionally, they attended Rutgers Robert Wood Johnson Medical School for Molecular Biology & Biochemistry, although specific dates and the completion of a degree are not provided.