We are looking for a Qualification & Cleaning/Sterilization Validation Subject Matter Expert (SME) to join our Technology Lifecycle Excellence (TLE) team.

In this role, you will lead and supervise qualification and validation activities across the site, ensuring systems, processes, and documentation meet the highest quality and regulatory standards, while maintaining a state of continuous inspection readiness.

This is a strategic, high-impact role requiring strong technical expertise, leadership, and cross-functional collaboration in a dynamic pharmaceutical environment.

Responsibilities

• Project Leadership & Execution
  • Lead and supervise site projects related to:
    • Equipment Qualification
    • Computer System Validation (CSV)
    • Cleaning & Sterilization Validation
  • Coordinate with cross-functional teams and global stakeholders to implement best practices and ensure compliance...