1 of 1 Management Information System Jobs in Waltham Abbey

minimum) As a Quality and Regulatory Affairs Manager at our client, you will play a key role in maintaining and developing their Business Management Systems and ensuring that all their in-vitro diagnostic medical devices meet stringent UK, EU, and international regulatory requirements. Your work will be central … integrity of their products and processes. Drawing on your expertise in ISO 17025 and wider regulatory frameworks, you will take ownership of their Business System Manuals and Technical Documentation, ensuring they remain robust, up to date, and audit ready. As the Management Representative for ISO … to uphold the highest standards of product quality, patient safety, and regulatory compliance. Main Objectives: To be responsible for all aspects of the Business System Manuals (Quality, Information Security & Environment) and medical device/in vitro diagnostic medical device regulatory compliance. To maintain and ensure adequacy and More ❯