Cleaning Validation Specialist
We are seeking an accomplished professional to lead qualification and validation activities in our Biopharmaceutical organization.
* Develop, review, approve, and execute qualification/validation documentation and cycle development studies.
* Implement change controls.
* Resolve technical issues during study execution.
Key Requirements:
* Experience in cleaning validation including CD & PQ of mobile vessels and parts washers, recipe development, and optimisation.
* Proven track record in delivering excellence in a GMP manufacturing setting.
* Relevant technical qualifications in Applied Pharmaceutical or Biological sciences.
* Exception/Deviation Management and Change Control.
* Leadership of technical projects.
* Knowledge of process monitoring systems and automation within a GMP manufacturing environment.
* Equipment and process validation.
As a Cleaning Validation Specialist, you will be responsible for ensuring the quality and integrity of our cleaning processes. If you have a strong background in cleaning validation and excellent communication skills, we encourage you to apply.