- Review and approval of all manufacturing batch documentation including electronic batch records, real time reports, master data using the site systems.
- Review and approval of SOP's, cleaning verification/validation data and other documents as necessary for the IPT department.
- Initiate and maintain Quality related metrics, ensuring effective communication and follow up of same.
- Provide effective real time on the floor support for day-to-day manufacturing operations for example area clearances, batch record reviews, aseptic operations.
- Bachelor's Degree or higher preferred; ideally in a Science, Engineering, or other technical discipline
- Relevant experience in a quality role, ideally in a pharmaceutical manufacturing environment
- GMP Audit experience in the pharmaceutical industry
- Knowledge of US and European cGMP guidelines, and other international regulatory requirements, as applicable to the site.
![](https://counter.adcourier.com/a2NvdWdobGFuLjYzNzczLjEyMzg4QGxzY2x0ZC5hcGxpdHJhay5jb20.gif)