Laurett Rivera

With experience leading in a GMP environment, including more than 15 years in progressively responsible team leadership roles in the biotech and pharmaceutical industries, Laurett is the Principal Consultant of Digital Transformation Manufacturing at USDM Life Sciences.

She has provided strategic direction and leadership to quality assurance and quality control functions. She’s also implemented mechanisms to drive compliance and control strategies that consistently achieve favorable audit results with a continuous state of inspection readiness.

Laurett has managed and executed comprehensive health authority inspections with positive outcomes, including the U.S. Food and Drug Administration (FDA), European Medicines Agency (EMA), and Pharmaceuticals and Medical Devices Agency (PMDA).

As a mentor and coach, Laurett guides high-performing cross-functional teams toward organizational goals. Her innovative solutions to complex problems boost compliance, cost savings, and efficiencies.

Her background in leading quality and manufacturing operations enables her to leverage her analytical and communication skills to achieve operational success and quality compliance.