Employee Spotlights

Beto Sanchez, Associate Director of Quality Assurance at Noble Life Sciences
"When starting a career as a Quality Assurance Professional I would recommend researching and joining the Society of Quality Assurance (SQA)."
Beto Sanchez, Ph.D.

Beto Sanchez, Ph.D.

Associate Director of Quality Assurance

Beto Sanchez joined the Noble team in 2021 as the Associate Director of Quality Assurance. He is responsible for the Quality Assurance and regulatory compliance at Noble and has over 20 years of experience with non-GLP/GLP pre-clinical research project management and regulatory compliance oversight. He is experienced with Quality Management Systems, root cause analyses, personnel training, Standard Operating Procedure (SOP) development, equipment management, study file administration and CFR Part 11 compliant software for Document Management Systems. His efforts have resulted in numerous successful FDA/EPA marketing applications.

Beto Sanchez, Ph.D.

Associate Director of Quality Assurance

Q: What do you like most about your job at Noble?

Beto: Ensuring transparency and regulatory compliance in everything we do.

Q: What are you most proud of in your career so far?

Beto: The improvements I see in how research staff document and apply their knowledge of GLP regulations.

Q: Do you have any tips for someone starting a career as a Quality Assurance Professional?

Beto: When starting a career as a Quality Assurance Professional I would recommend researching and joining the Society of Quality Assurance (SQA). The SQA provides numerous educational and training opportunities and hosts an annual meeting every year to discuss quality matters and regulatory updates.

Q: Do you have any hobbies or what do you enjoy most when you’re not at work?

Beto: Coaching, spending time with family, working out and traveling.

Q: Who is someone that has made a big impact on your life? Why?

Beto: Dr. Mohan Suntha, President and Chief Executive Officer of the University of Maryland Medical Center (UMMC). Back when he was a resident he taught me the importance of hard work, education, integrity and family.

With decades of GLP experience, our scientists can support all aspects of the GLP process, from design to regulatory support of your IND, IDE, or PMA FDA submission. Learn more about our quality practices here.

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