Quality Management System (QMS) Documentation and Training Content to Support Operational Readiness for US-Based Pharmaceutical Company

Bold Statement Markets Pharmaceuticals Services Provided Quality & Compliance The project kicked off with an initial strategy workstream to define the overall ways of working, to assign roles for all team members, and to onboard the project management team. To begin the implementation phase, Kymanox performed a gap assessment of existing Quality Management System (QMS)…

The project kicked off with an initial strategy workstream to define the overall ways of working, to assign roles for all team members, and to onboard the project management team. To begin the implementation phase, Kymanox performed a gap assessment of existing Quality Management System (QMS) processes and documentation to determine what content the new site could leverage from the other global sites in order to minimize implementation costs. Once a full accounting of the available information was completed, Kymanox began developing new or revised documents and training content with some improvements incorporated where feasible.

Challenges

A Fortune 500 US-based pharmaceutical company needed support in the development of their site’s QMS and associated training programs required for Good Manufacturing Practices (GMP) operational readiness at a new site under construction.

Key Objectives

  • Drafting comprehensive documents for the new facility from leveraged materials such as existing policies and procedures and creating them from baseline reference materials available.
  • Collaborating with personnel from multiple departments within the client company: Operations, Engineering, Quality Assurance, Quality Control, Logistics & Supply Chain, Manufacturing Sciences, and others.
  • Working directly with subject matter experts (SMEs) to draft, review, and approve all documentation and training content.
  • Producing cost savings and efficiencies by combining or simplifying documentation and training content where possible.
  • Facilitating risk assessments to ensure training was assigned to site QMS procedures based on the perceived risk to patient safety.
  • Producing training content to include eLearning/Computer-Based Training (CBT), Instructor-Led Rraining (ILT), assessments, and On-the-Job Training (OJT) modules.
  • Tracking and reporting monthly on the deliverables, budget, and any project concerns.
  • Finalizing the client’s QMS and phasing out the technical writing component of the project.
  • Ensuring all work could stand the test of a regulatory body inspection to allow for commercial success.

Solutions

Kymanox experts assisted the client with building the QMS system and offering continuous support over a multi-year contract. Kymanox conducted gap assessments of existing QMS processes and documentation​. Then our team of experts worked cross functionally with multiple departments and subject matter experts to develop QMS documents and training content​. We also created risk assessment & training assignments to produce various training content.

Result

  • Performing gap assessments for continual monitoring of compliance with client standards and regulatory expectations.
  • Supporting the technical writing of procedures, child documents, and training content during the site start-up period in line with the operational readiness schedule for the facility and equipment.
  • Collaborating with subject matter experts to create the training materials necessary to support site operations.
  • Committing to acclimate new hires to the pharmaceutical industry while working alongside them to build the QMS