**ABOUT UNILEVER**
Unilever is the place where you can bring your purpose to life with the work that you do - creating a better business and a better world. You will work on brands that are loved and improve the lives of our consumers and the communities around us. You will lead innovations, big and small, that will make our business win and grow. You will learn from brilliant business leaders and colleagues who provide mentorship and inspiration so that you can become a better you.
**JOB PURPOSE**
If you want to be part of Unilever´s history, as being part of the creation of a completely new site that has the expectation to be a state of the art and future fit factory, a model for other sites to reference both internally and externally, then this role is just for you!
**WHAT WILL YOUR MAIN RESPONSIBILITIES BE**
- Leads effort to verify and document compliance to regulatory requirements applicable to quality and consumer safety, and to ethnic and religious requirements. Includes the FDA
- Implementation of UL Quality Management System (QMS) in Veeva Quality One at the site to assure consumer safety and overall quality of final product being manufactured
- Review process and management of the factory SOPs/Document Management through Veeva Quality One to ensure that UL and other applicable standards are accurately represented
- Leads the factory Management of Change program
- Manages SAP QM Systems and Unilever specifications including PLM and supports verification of use for quality purposes
- The implementation and maintenance of systems where key quality data and information are recorded and preserved and assures, they meet regulatory requirements
- Drives quality focus improvement activities through the use of advanced tools such as SPC and digital capabilities
- Leads efforts to complete and maintain external audits and certifications
- Leads finished goods holds and releases
**EXPERIENCES & QUALIFICATIONS**
- Bachelor's Degree
- 2-4 years of Manufacturing
- A minimum of 3 year of related Quality experience
- FDA experience