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Posted 3 days ago by SRG
Management of controlled documentation e.g., SOPs, Work instructions, Forms, Policies. Develop procedures so that they are standardised. Ensure that all documents are up to date, maintaining applicable registers. Scanning of documentation. Train employees on how to use and access documents. … more
Posted a week ago by Evolve Personnel
Post market surveillance and post market clinical follow up plans. Completing post market surveillance reports. Involvement in customer complaint investigations. Assisting with internal audits. Maintaining SOPs and other QMS documents. Assisting with internal product reviews. Managing</ … more
Posted 17/04/2024 by Wright Staff Recruitment Ltd
As part of our expansion plans, the company is looking for a PMS/QA Associate to gather and collate clinical data to meet regulatory requirements, and to help develop and maintain the quality system that underpins the business. This person will report to, and provide quality … more
