Keyskills :
                            Manufacturing , Analysis , Biomedical Engineering , Catheter , Collaboration , Communication , Compliance , Design , Development , Documentation , Documentation Development , Equal Employment Opportunity , Guidance , Hazard Analysis , Implementation , Inclusive , ISO 13485 , ISO 14971 , Management , Manufacturing Process , Mechanical Engineering , Medical Device , Medical Device Regulations , Optimization , Oral and Written Communication , Orientation , Process Improvement , Process Optimization , Process Validation , Product Development , Product Quality , Proper Documentation , Quality Metrics , Regulatory Standards , Revision , Risk Management , Root Cause Analysis , Study Design , Team Player , Tooling , Validation , Work Instructions , Written Communication                            
                        
                        Designation:
                            
                                N/A
                            
                        
                                                        
                                    Job Description:
                                    
                                         Title: Quality Manager (Engineer background) Status: Full-time, Exempt Reports to: Director of R&D Our team is dedicated to developing technologies that will change the medical device landscape. If you are seeking an opportunity to make a real impact on pa…