Azzur Group is a GxP compliance and consulting organization focused on providing quality-driven solutions that propel life science companies toward success. If you're a dedicated professional with a desire to engage, learn, and adapt within a dynamic healthcare landscape, you will fit right into our core values: Put Others First, Have the Courage to Take Action, Take Personal Responsibility, and Have Fun!

This position requires expertise in cleaning validation and monitoring in a cGMP facility. Key requirements include:

Hands-on experience with CIP/SIP systems, washers, vessels, tanks, and manual cleaning. Development and execution of cleaning validation protocols and reports. Troubleshooting and optimizing CIP/COP systems, with experience in cycle development preferred. Data analysis and presentation of results, ensuring adherence to project specifications and timelines. Generation and resolution of protocol discrepancies. Review of GxP deliverables (specifications, procedures, validation documents). Training of operations staff on relevant protocols and procedures. Organization and tracking of validation activities to meet client timelines. Experience with various sampling techniques. Strong knowledge of cGMP requirements and excellent communication skills. Preferred skills: experimental design, problem-solving, organizational abilities, project management, discrepancy reporting, and root cause analysis experience.