SRG are currently in partnership with one of the world's leading specialised medical diagnostic companies. They are leading the way in delivering innovation to the medical devices sector and you will have the opportunity to meet some of the industry's biggest challenges and opportunities head on. They are looking to a fulfil a position within their company for a QA Specialist.
To contribute to the development of policies and procedures within their area of specialism and ensuring that these are implemented and compliant with the quality system. To report the status of their area of responsibility to senior managers as required. To be responsible for planning their own workload and work without day‐to‐day input from manager, influencing own personal development and establishing appropriate timelines for long‐term projects. To co‐ordinate workload and set objectives for staff member(s) assigned to assisting with their area of specialism to ensure that the operational objectives of the department are met and delivered within agreed timelines. To be responsible for ensuring quality within validation activities across the company, evaluate validation activities and suggest improvement initiatives to ensure that departments are performing validation as efficiently as possible. To take full responsibility for understanding their key areas of responsibility and ensuring that they are understood and followed throughout the company.Candidate requirements:
Previous experience of working in a quality system environment, preferably within medical devices or similar. Extensive knowledge of Computerised Systems Validation within a medical device or similar environment.Desirable:
Previous management experience. Ability to deputise for department manager as required. Working knowledge of process validation and equipment qualification. Understanding of Data Integrity regulations applied to Medical Device (or similar) manufacturing. If this role sounds of interest to you, please apply below for more information