A pharmaceutical manufacturing company is seeking a skilled professional to oversee the commissioning, qualification and validation of lyophilisation systems. This role involves developing documentation, leading CQV activities and supporting project adherence.
About the Role
* Oversee commissioning, qualification and validation of lyophilisation systems
* Develop documentation for quality control purposes
* Lead CQV activities to ensure compliance with regulatory standards
The ideal candidate will have over 5 years' experience in a GMP environment and excellent knowledge of regulatory standards. They will be responsible for enhancing efficiency and compliance within the CQV function.