Medical Device Post Market
Medical Device Post Market Surveillance
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.
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.
Medical Device 5 years
Post Market Surveillance
Job Type: Contract