Prepare for and participate in internal and external Project Kick-Off Meetings to evaluate contractual quality obligations, clarifications and deviations.
Perform dimensional and functional inspections on First Article (FA), incoming, in-process, and outgoing parts according to work instructions and specifications.
Develop and implement strategic sourcing and commodity strategies, including supplier negotiations, commercial agreements and cost reduction initiatives.
To work in close coordination with SPS Quality Lead for SPS quality assurance / controls activities, and equipment delivery and handover coordination activities.
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
Serve as the Quality Engineer for assigned product technologies and manufacturing processes, ensuring compliance with quality requirements and customer expectations.