1 to 6 of 6 Permanent Market Surveillance Jobs in the UK with Remote Work Options

Product Manager Salary: £60,000 - £80,000 Location: London/Bristol - Hybrid Skills : Trade Surveillance, Market Surveillance, Market Abuse, eComms Surveillance, TCA, Regulatory Reporting, Best Execution, MAD2, MAR2, Mifid2 Are you looking for an excellent opportunity to join an exciting vendor who provide Regulatory and … Surveillance & Analytics tools to the financial services industry who require a Product Manager to join there expanding team. As a Product Manager within this leading provider of Regulatory Technology(RegTech), you will be working very closely with development teams and clients translating requirements for functional and technical specifications. My … of clients in flight and is under resourced with the technical and functional knowledge and know how to enhance their systems to compete with market leading financial services platforms. To be considered for the role of Product Manager the following experience is essential; knowledge of Trade, Market or more »

Junior Consultant with 2-5 years of experience in Regulatory Affairs. This role requires hands-on involvement with the management of technical files, post-market regulatory activities, global device registration, and formulating regulatory strategies. Quality Assurance experience is an added advantage. Key Responsibilities: Regulatory Submissions: Prepare and submit regulatory … medical devices. Compliance Monitoring: Monitor and interpret regulatory requirements, ensuring that company products and practices are in compliance with relevant regulations and standards. Post-Market Surveillance: Conduct post-market surveillance activities, including adverse event reporting and PMS reports. Validation Testing: Participate in the planning and execution … Assist in the preparation and maintenance of Clinical Evaluation Reports (CER). Regulatory Strategy: Support the development of regulatory strategies for new products and market entries. Stakeholder Communication: Liaise with internal and external stakeholders, including regulatory bodies, to address queries and provide regulatory guidance. Key Qualifications: 2-5 years more »

Junior Consultant with 2-5 years of experience in Regulatory Affairs. This role requires hands-on involvement with the management of technical files, post-market regulatory activities, global device registration, and formulating regulatory strategies. Quality Assurance experience is an added advantage. Key Responsibilities: Regulatory Submissions: Prepare and submit regulatory … medical devices. Compliance Monitoring: Monitor and interpret regulatory requirements, ensuring that company products and practices are in compliance with relevant regulations and standards. Post-Market Surveillance: Conduct post-market surveillance activities, including adverse event reporting and PMS reports. Validation Testing: Participate in the planning and execution … Assist in the preparation and maintenance of Clinical Evaluation Reports (CER). Regulatory Strategy: Support the development of regulatory strategies for new products and market entries. Stakeholder Communication: Liaise with internal and external stakeholders, including regulatory bodies, to address queries and provide regulatory guidance. Key Qualifications: 2-5 years more »

compliant to EU/UK MDR (Medical Device Regulation) Identifying, interpreting, evaluating and incorporating information from various sources appropriate to the device Analysing post-market surveillance data and risk management data to ensure consistency and alignment in CER (Comparative Effectiveness Research) Evaluating clinical evidence from published literature, post … market surveillance, risk assessments and post-market clinical data, and be able to generate a report of these data Ensure that Clinical Evaluation Plans/Reports and databases are kept compliant and up to date Managing timelines and communication to ensure deliverables and milestones are met Assisting more »

and monitor established policies and procedures to ensure compliance with necessary regulatory bodies in the areas of: Corrective and Preventive Action (CAPA), Complaint, Post Market Surveillance and Non-conformance Report (NCR). Provision of advice according to established procedures relating to CAPA, Complaint, Post Market Surveillance … Employee Assistance Programme About ATL Technology ATL Technology is a fast-growing provider of outsourced design, development and manufacturing services to the medical device market, and its UK site is based in St Mellons, Cardiff. We believe that there is a better way to bring medical devices to market more »

and monitor established policies and procedures to ensure compliance with necessary regulatory bodies in the areas of: Corrective and Preventive Action (CAPA), Complaint, Post Market Surveillance and Non-conformance Report (NCR). Provision of advice according to established procedures relating to CAPA, Complaint, Post Market Surveillance … Employee Assistance Programme About ATL Technology ATL Technology is a fast-growing provider of outsourced design, development and manufacturing services to the medical device market, and its UK site is based in St Mellons, Cardiff. We believe that there is a better way to bring medical devices to market more »