Please refer to JobSuchmaschine in your application
– Prepare the product and quality documentation for those innovative systems.
– Write the suppliers specifications.
– Write the testing specifications.
– Be the interface with the different suppliers (product; medicine and packaging suppliers) and the different departments (quality, validation, procurement, etc.) within the company.
– Engineer diploma or equivalent in medical device field
– ISO 13485 knowledge mandatory
– Experience in glass pre-fillable syringes is a plus
– Willingness to work in an international environment
– English and German spoken and written