Jennifer Strand

Jennifer Strand has extensive work experience in the biopharmaceutical industry, specializing in quality systems and compliance. Jennifer is currently the Director of Quality Systems & Compliance at Oxford Biomedica Solutions, a role they assumed in August 2022. Prior to this, they served as the Associate Director of Quality Systems and Compliance at the same company from April 2022 to August 2022.

Before joining Oxford Biomedica Solutions, Jennifer worked at Homology Medicines, Inc. from 2019 to 2022. Jennifer held various positions at Homology Medicines, starting as a Senior Validation Manager in September 2019 and progressing to Associate Director of Validation & Quality Risk Management in April 2021. In their last role at Homology, they were responsible for the oversight of quality systems and compliance.

From 2016 to 2019, Jennifer worked at Shire as a QA Manager and Senior Cleaning Validation Engineer II. Prior to Shire, they worked at Bristol-Myers Squibb, where they held the positions of Project Lead and Lead Validation Engineer from 2011 to 2016.

Jennifer's career in the biopharmaceutical industry began at Pfizer (formerly Wyeth Biotech), where they worked as a Validation Specialist III from 2006 to 2011. Jennifer also gained experience at Genzyme Genetics as a QC Analyst and at Veolia Water as a Lab Sales and Marketing Specialist.

Jennifer Strand obtained their initial laboratory experience at Charles River Laboratories, where they worked as a Senior Technologist/Technologist from 2001 to 2003. Jennifer holds a strong foundation in laboratory techniques and processes.

Throughout their career, Jennifer has acquired extensive expertise in quality systems, compliance, validation, and risk management within the biopharmaceutical industry. Their diverse roles and responsibilities demonstrate their ability to adapt and excel in varying capacities.

Jennifer Strand completed their Bachelor of Science degree in Biology at the University of Massachusetts Lowell from 1997 to 2001.