Oversee effective implementation of the QMS throughout the company including management of FMEA, control plan, change control, documentation and internal/external audits
Set up, start, operate, stop, and adjust plastic machining equipment according to approved work instructions, engineering drawings, and production requirements.
Provide QA oversight for RSTO to ensure that investigational medicinal products (IMPs) and commercial medicinal products are manufactured in accordance with global Roche, Pharmaceutical Quality System (PQS) and local site requirements
Lead and manage end-to-end integration projects for new data centre capacity, ensuring projects are completed on time, within budget, and to the required quality standards.
Implementing and monitoring quality assurance and quality control (QA/QC) procedures to ensure compliance with project specifications, approved drawings, and relevant industry standards.