A Proven Experience: QMS and MES on a Unified Platform

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Key Takeaways

Why Attend?

  • Learn how integrating quality and manufacturing functions on a unified platform ensures seamless connectivity, leading to the production of safe and effective products
  • See how flexible systems support life science manufacturers, including contract manufacturers and 503B outsourcers, in managing the production of multiple products.
  • Understand the specific features and functionalities of a platform that caters to high variability life science manufacturing.

About This Event

Ensuring quality is a fundamental aspect of life science manufacturing, crucial for producing impactful, safe, and effective products. Achieving seamless connectivity between quality and manufacturing functions is key. One proven solution is integrating quality and manufacturing systems on a unified platform. Join Jennifer Rodriguez, Corporate Quality Systems Manager at QuVa Pharma, as she shares her insights on leveraging a closed-loop, single-platform approach. Jennifer will present real-world data and everyday experiences that highlight the benefits of integrating your quality management system (QMS) and manufacturing execution system (MES).

About QuVa Pharma

QuVa is an industry-leading FDA-registered 503B outsourcing services company that provides hospitals with essential medications in ready-to-administer injectable formats that are critical for effective patient care. QuVa was purpose-built to change the 503B industry for the better and is leading the way with its significant expertise in cGMPs and sterile pharmaceutical manufacturing, and a focus on ensuring compliance with the highest quality and safety standards.

Key Takeaways

Why Attend?

  • Learn how integrating quality and manufacturing functions on a unified platform ensures seamless connectivity, leading to the production of safe and effective products
  • See how flexible systems support life science manufacturers, including contract manufacturers and 503B outsourcers, in managing the production of multiple products.
  • Understand the specific features and functionalities of a platform that caters to high variability life science manufacturing.

Jennifer Rodriguez

Corporate Quality Systems Manager

QuVa Pharma

Jennifer Rodriguez is a seasoned quality systems manager with over 18 years of experience in quality assurance, program management, and continuous improvement. She currently serves as the Corporate Quality Systems Manager at QuVa Pharma, Inc., where she has worked since August 2016. Jennifer has extensive experience in configuring quality management systems and continuous improvement programs. She holds a degree in System Engineering from Pontificia Universidad Javeriana, is a MasterControl Certified Expert, and has earned Greenbelt Six Sigma certification.

Katie Farley

Director, Product Management at MC Research Labs

MasterControl

Katie Farley is a product management director at MasterControl, where she collaborates with customers, engineering, quality, and other cross-functional teams to complete software product roadmaps that accomplish user needs. In this role, she has been actively involved in defining and developing MasterControl’s one-of-a-kind Manufacturing Excellence solution, as well as been responsible for the early-adopter program that brought the solution to market for life sciences manufacturers. Farley has 10 years of experience in management and recruitment positions within various industries, most with an emphasis on IT. She earned a Certified ScrumMaster certification and is a Scaled Agile Framework (SAFe) 4 certified product owner/product manager. Farley holds a bachelor’s degree in international business management and German from Western Washington University and a master’s in management information systems from the University of Utah. 
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