Main Purpose of the position is to lead and execute process improvement projects at supplier and internal sites to ensure reliable Direct Material supply in collaboration with cross functional and supplier representatives to bring comprehensive solution to trending and recurring Direct Material issues.
You lead supplier site technical visits to review and assess Direct Material manufacturing processes and capabilities. In addition you proactively identify and ensure anticipated issues are sustainably addressed using quality engineering tools to effectively support new supplier site introductions, supplier site transfers, and new technology introduction at supplier site.
Your main responsibilities are to :
ups through quality engineering activities and oversight at the supplier site, in collaboration with internal relations and in conjunction with overall change management activities
Who you are :
You have a University degree in Life Sciences e.g. Chemistry, Chemical Engineering, Engineering, Pharmacy, Biochemistry and at least ten years’ professional industrial experience (pharmaceutical, biopharmaceutical or related industry is a plus), or an equivalent combination of education and experience.
You have a sound knowledge of cGMP’s, ISO standards and international regulations. You bring solid knowledge and experience in at least two of the following areas : drug, medical device, or biologic manufacturing processes, Supplier Quality, laboratory test methods, sterilization, and validation processes.
In addition you bring the following skills and competencies :
This role requires international travel up to 20%.
focused healthcare groups. Our success is built on innovation, curiosity and diversity.
Roche is an equal opportunity employer.