Medical Device Post Market

Minneapolis, MN

Job ID: 122841 Industry: Med

                                                    Medical Device  Post Market  Surveillance 

Environment:
Our client is a leading supplier of specialized medical devices and equipment for global markets, focusing on the medication delivery, vital care and safety devices market segments. They need a Quality Engineer that will be focusing on Post Market Surveillance and Risk Management for their design team.

Job Duties/Responsibilities:
Our client is looking for a Quality Assurance Consultant  that will be supporting the Quality team in various ways. They will be responsible  for post market surveillance and updating their legacy files and procedures. They will be in charge of  re-looking at  how they  conduct post market surveillance  activities and what is critical to the customer. They are in the midst of launching a new product and they want to make sure they are delivering the right strategies.  They will also be assisting the R&D team by understanding and creating linkages between risk management and complaint specifications.   They will need to compare risk management to the field reports through MDRs and complaints.  They will be responsible for ensuring product complaint investigations are accurate, thorough and compliant. They will also support risk assessment activities associated with product failures.

Required:

Medical Device 5 years

Post Market Surveillance

Risk Management

Job Type: Contract 

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