Management (37.2 Agreements, Vetting, booking of medicals, compiling of safety files, booking of required
maintain regulatory compliance against ISO 13485 and Medical Device Directives, MDD 93/42/EEC, and will be based Experience 3-5 years of experience in the laboratory / medical device industry Total Quality Management System
Implement a Stability Master Plan. Experience in Medical Devices 2. COMPLAINTS To ensure that all product
Implement a Stability Master Plan. Experience in Medical Devices 2. COMPLAINTS To ensure that all product