Regulatory Compliance Jobs in Guildford

2 of 2 Regulatory Compliance Jobs in Guildford

Principal Agentic Solutions Consultant

Guildford, Surrey, UK
Hybrid/Remote Options
Aveni
financial services domain experience to drive enterprise-wide productivity. We're using the latest in AI to automate and innovate, empowering financial service businesses to achieve exceptional productivity and compliance outcomes. Role Overview As a Forward Solutions Engineer/Principal Solutions Consultant at Aveni, you will be a key technical leader in pre-sales, solution design, and customer engagement. … to define, architect, demonstrate, and deliver AI-powered solutions tailored to banks, wealth managers, insurance firms, and other financial services clients. Your mission is to translate complex business and regulatory needs into scalable, robust, compliant solutions that underscore Aveni's value proposition. You will often be "forward deployed", meaning you'll engage closely with strategic clients, acting as subject … From this background you bring: Rigorous client-facing experience: doing discovery, scoping, workshops, POCs, RFPs, not just writing proposals, but engaging deeply with clients at multiple levels (operations, risk, compliance, executives). Structured, analytical problem solving: you break down fuzzy business problems, diagnose root causes, map them to technical and regulatory constraints, and propose robust, scalable solutions. High More ❯
Employment Type: Full-time
Posted:

Regulation & Quality Lead

Guildford, Surrey, UK
Physitrack PLC
Your primary focus will be to prepare the organisation for MDR/UKCA certification. This role is ideal for someone who enjoys bridging the gap between product, engineering, and compliance in a fast-moving digital health environment. You will work closely with our Product, Engineering, and Clinical teams across the full product lifecycle of the Physitrack and Champion Health … platforms. Your mission will be to ensure that our Quality Management System (QMS), risk management, and compliance processes evolve as our products move towards medical device status under MDR and UKCA frameworks. You will collaborate with internal stakeholders — including our Information Security and Legal teams — and manage relationships with external regulatory consultants. This is a hands-on role … about building quality into products, not just maintaining documentation. The ideal candidate will have experience with Quality Management Systems (ISO 13485/ISO 9001), Medical Device Software (SaMD), or Regulatory Compliance in a digital health or wellness environment. However, we are also open to hearing from candidates with deep experience in one of these areas and a strong More ❯
Employment Type: Full-time
Posted: