Quality Engineer
Crawley, Sussex, United Kingdom
Elekta AB
similar role. Training and experience in relevant medical device regulatory requirements and standards (e.g. ISO, IEC, MDR, MDSAP). Lead audit trained in ISO13485/9001 Proven experience in relevant areas of Quality, Regulatory, or Engineering, preferably within a medical device environment. Strong written and verbal communication skills and More ❯
Employment Type: Permanent
Salary: GBP Annual
Posted: