Site Validation Activities
Our organization is currently recruiting for a Cleaning Validation Engineer to support site validation activities across various workstreams.
This role involves developing and maintaining the site Validation Master Plan, driving development of site cleaning strategy and implementing/maintaining cleaning and sanitisation protocols and procedures for pharmaceutical equipment.
The successful candidate will perform risk assessments to determine the criticality of cleaning processes, set acceptance criteria, oversee cleaning validation studies and ensure proper execution, data collection, and documentation.
Collaboration with production and maintenance teams is essential in establishing cleaning procedures and validating requirements. Drafting, reviewing and approving related documentation is also a key responsibility.