Pedro M Bento

About Pedro M Bento

Dynamic Leader with 20+ Years of Transformational Success in Pharmaceutical Quality Assurance and Operations.Problem solver executive with a distinguished track record of leading high-performing teams and driving enterprise-wide Quality Assurance and regulatory compliance initiatives within the pharmaceutical industry. Expertise spans Quality Systems management, process validation, operational excellence, and regulatory compliance, with a focus on enhancing efficiency, mitigating risk, and exceeding industry standards.Proven ability to design and implement innovative quality strategies that deliver measurable results, improve product integrity, and ensure alignment with global regulatory frameworks. Adept at fostering collaborative relationships with internal and external stakeholders, building consensus across diverse organizational levels, and inspiring teams toward a shared vision.Recognized for customer-focused leadership, team-building acumen, and conflict resolution expertise, driving sustainable growth and operational excellence in fast-paced, highly regulated environments.

Experience

1. Senior Director - Group Lead, Quality Systems & Compliance

   Dr. Reddy's Laboratories

   Apr 2023 — Present

Education

• Centenary University

  Master of Business Administration (M.B.A.)

• University of Nebraska at Kearney

  Master of Science (MSc), Biology

• Kean University

  Bachelor's Degree, Biology, General

Skills

• Quality Assurance
• U.s. Title 21 Cfr Part 11 Regulation
• Verification and Validation (V&V)
• Gmp
• Computer System Validation
• Change Control
• Good Laboratory Practice (Glp)
• U.s. Food and Drug Administration (Fda)
• Pharmaceutical Industry
• Sop
• Fda
• 21 Cfr Part 11
• Standard Operating Procedure (Sop)
• Regulatory Affairs
• Validation
• Capa
• Gxp
• Quality System
• V&V
• Laboratory
• Corrective and Preventive Action (Capa)
• Glp