We are looking for a Regulatory Affairs Specialist for medical devices who will be responsible for planning, leading, and executing regulatory activities in R&D projects for international clients from the Medical Devices and Products sector. You will work closely with teams across sites under design control and ensure that the client adheres to internal QMS and our Risk lifecycle process.
Your roleJob no. 241015-BRCKU
Bring them to Sii and receive a bonus (fill in the form in English please)
Are you sure you want to leave this page?
Ви справді бажаєте залишити цю сторінку?
Ви справді бажаєте залишити цю сторінку?