Roles and Responsibilities: To work on Complaint handling Process – Evaluation, Regulatory Assessment, Investigation Work with lead in completing daily assignation. Organize and manage daily work allocation Complaints remediation using work instruction, compliance to process To drive efficiency and compliance. Collaborate with of cross function team (CFT) such as Intake, MDR, Investigation to execute the project and initiative.Skills: 5 to 12 years of experience in Medical devices complaints handling For Complaint Investigation – Mechanical problem analysis skill needed An excellent communicator, both written and verbal Adopt to cross cultural differences Ability to work in a timeline driven environment Proficiency using tools such as Trackwise, Sales force, Service MaxEducational Qualification:B.E./B.Tech (Bio-Medical, Mechanical), B.Pharm, BSc Bio ScienceExperience - 5 to 12yrs Immediate joiners can apply (notice period not more than 30 to 45days)
Job Title
Lead Engineer - Post Market Surveillance