Within a world leading contract manufacturer and developer specialized in aerosol, semi-solid and liquid pharmaceutical products.
- The operations of manual conditioning according to a defined modus operandi and in the respect for Good Manufacturing Practice (GMP)
- The qualitative controls and checking the consumption of raw material.
- File a record or a description of controls that are in place during manufacturing and conditioning to ensure the labelled amount of medicinal and corresponding packaging.
- Verification and maintenance of records
- Verification of the final product before launch into the industry.
Learnd to be rigorous, to work within a big corporation and gained technical skills.