Job Title: Medical Safety Analyst DevicesLocation: SittingbournePay Rate: £23-£30 per hourDuration: 12 MonthsResponsibilities:Process consumer complaints related to enteral feeding medical devices in accordance with applicable regulations.Collect, assess, and document medical device complaints and adverse events promptly and compliantly.Conduct follow-up calls with customers to gather additional details on adverse events and complaints.Code complaints usin
Job Title: Medical Safety Analyst DevicesLocation: SittingbournePay Rate: £23-£30 per hourDuration: 12 MonthsResponsibilities:Process consumer complaints related to enteral feeding medical devices in accordance with applicable regulations.Collect, assess, and document medical device complaints and adverse events promptly and compliantly.Conduct follow-up calls with customers to gather additional details on adverse events and complaints.Code complaints usin
Do you consider yourself to be an organised individual, with great communication skills? Are you able to work effectively to provide procedural reports and updates? If so, we are looking for an individual who would be interested in joining a UK EHS Commercial Manager. You will be responsible for a number of tasks from supporting issues or incidents, conducting reviews and chairing committee meetings.Role details:Title - UK EHS Commercial ManagerLocation -
Do you consider yourself to be an organised individual, with great communication skills? Are you able to work effectively to provide procedural reports and updates? If so, we are looking for an individual who would be interested in joining a UK EHS Commercial Manager. You will be responsible for a number of tasks from supporting issues or incidents, conducting reviews and chairing committee meetings.Role details:Title - UK EHS Commercial ManagerLocation -
Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so, our Biotechnology client is looking for individuals just like you! The successful candidate will perform quality review to ensure documents authored by the Safety Surveillance and Aggregate Reports team or their vendors are of high quality and support process improvement. This is a contract position offered initially on a 12 month contract basis working
Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so, our Biotechnology client is looking for individuals just like you! The successful candidate will perform quality review to ensure documents authored by the Safety Surveillance and Aggregate Reports team or their vendors are of high quality and support process improvement. This is a contract position offered initially on a 12 month contract basis working
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