Abstract
This presentation offers Project Managers in software companies that support the Life Sciences industry a step-by-step guideline to design and implement a scalable Quality Management System (QMS). Tailored for organizations that develop enterprise software solutions for pharmaceutical and MedTech companies, the session emphasizes how to align QMS frameworks with regulatory compliance, audit readiness, and industry best practices.
Learning objectives:
Attendees will gain practical insights on building a QMS that not only supports software development and delivery but also ensures long-term scalability, adaptability, and compliance in an evolving life sciences landscape.
Registration
- $0.00 - PMINJ Chapter members
- $5.00 - Non-members (no refund)
- The link to the virtual meeting will be included in
the Registration Receipt
- Download the Zoom app at: https://zoom.us/download
Speaker
Trupti Shinde
With over 15 years of experience leading projects and teams in the pharmaceutical industry, Trupti Shinde brings deep expertise in Program Management, Strategic Communications, Project Management, and Compliance Management across both Agile and Waterfall methodologies. Her career has been defined by establishing and enhancing Quality Management Systems (QMS), driving compliance, and optimizing processes to meet evolving industry demands.
Trupti specializes in building and developing scaling strategies for organizational digital transformation initiatives, enabling companies to modernize operations and achieve sustainable growth. She excels at leading cross-functional teams to ensure projects align with organizational strategy while meeting audit requirements and industry benchmarks.
Guided by a mission to uphold the highest standards of quality, Trupti is driven by a commitment to excellence, adaptability, and delivering lasting value in the pharmaceutical sector.
