1 to 13 of 13 Market Surveillance Jobs

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 »

THE COMPANY: Our client is one of the largest commodities houses in the world. They are looking to hire a Market Abuse Surveillance Expert for their London team. THE RESPONSIBILITIES: Conduct daily market abuse and market integrity surveillance Develop the Market Surveillance systems … and processes to ensure the surveillance programme remains robust and effective. Handle referrals and investigations undertaken by Market Surveillance. Responding to requests for information from the FCA. Keep abreast of market and regulatory news that may impact the surveillance programme. Ensure that a full audit trail … are accurate and completed to the highest standard. Draft and update procedure manuals as and when required. Provide support to the rest of the Market Surveillance team on day to day tasks or special projects when required. EXPERIENCE REQUIRED: Surveillance experience is key Metals experience – precious and 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 »

a profitable client orientated Global FX Franchise. Particular focus will be on developing strong liquidity relationships and optimising for high-volume FX flow, increasing market share and profitability. Key Activities: Monitor developments of flow and risk in the SGX OTC ECN Venue in London and Singapore during LDN and … NY Time Zone. Monitor and ensure efficient flow matching in London and Singapore instances on a micro level. Market Surveillance, Risk Monitoring at Central Prime Brokers and participants levels. Work with Project, Product, Integration and Development teams to deliver continuous performance improvement. Maintain contacts and relationship building within … interest in financial markets. Ability to apply systematic techniques to identify quality client flow, improve volume and optimise fill ratios. Knowledge of how FX Market Makers provide liquidity and the techniques used for successful market making. Strong track record of Client engagement and an excellent ability to communicate more »

processes and reviewing and reporting on root cause analysis Compliance oversight of financial promotions issued by the firm. Investigation of suspicious transactions and orders (market surveillance). Assisting in the administration of the Senior Managers and Certification Function Regime. Assisting in the documentation of internal controls, policies, and more »

responsible to maintain the effectiveness of the Quality Management System, including, but not limited to, Document Control, CAPA, Vigilance, Risk Management, Internal Audit, Post-Market Surveillance, Supplier Monitoring and Assessment and Product Release activities Contribute to strategic improvement projects to improve business processes in line with the applicable more »

responsible to maintain the effectiveness of the Quality Management System, including, but not limited to, Document Control, CAPA, Vigilance, Risk Management, Internal Audit, Post-Market Surveillance, Supplier Monitoring and Assessment and Product Release activities Contribute to strategic improvement projects to improve business processes in line with the applicable more »

IVD Directive (98/79/EC). Lead strategies for a large product portfolio including supporting new registrations, authoring technical files, and post-market surveillance. A minimum of 8 years post-qualification experience in regulatory affairs in the medical device and/or pharmaceutical industry in product registration more »

both headcount and AUM. The role offers the opportunity to join a highly prestigious hedge fund that has very low attrition -they offer a) market leading compensation packages, b) incredible benefits , c) some of the best internal progression platforms of any London based hedge fund - hence why its employees … aspects of compliance for the business. Working as part of a team of 3, in a flat structure, responsibilities will extend across monitoring, marketing, surveillance, distribution and advisory. Tech is core to their business and you can expect to fully develop these skills and be involved in various automation … globally. They are flexible on salary for the role – the right candidate will receive a guaranteed strong base salary uplift, as well as a market-leading bonus on top of this. more »