4 of 4 Regulatory Compliance Jobs in Cambridge

Description Summary At Sandoz, our Purpose is pioneering access for patients. The Regulatory Information Management Systems (RIMS) and Digitalisation role blends regulatory domain expertise, systems leadership, digital transformation capability, and a strong focus on automation and AI‐enabled process optimisation. The successful candidate will be a key member … responsible for system definition, selection, implementation, and continual improvement of RIMS platforms, business processes, automation solutions, and emerging AI technologies to deliver high‐quality regulatory data and efficient submission operations. Responsibilities Own the global RIMS strategy and ensure the system supports end‐to‐end regulatory processes, data standards ...

remaining hands‐on in design and problem solving. You will build and guide a high‐performing team across electronics, firmware, software and mechanics, ensure regulatory compliance, and deliver reliable, high‐precision control for complex automated instruments. #J-18808-Ljbffr ...

trials. About the role As Qureight scales, we are building the operational backbone required to deliver at pace, without compromising on scientific rigour or regulatory compliance. We have strong commercial traction with global biopharma partners and the infrastructure, workflows and quality frameworks needed to support complex global trials. … enhanced maternity leave A diverse work environment that brings together experts in many fields, including software engineering, devops, data science, machine learning, quality assurance, regulatory affairs, and clinical operations. Closing date for applications is Wednesday 12th August @ 17.00. Please note: Previous applicants do not need to re-apply ...

Opportunity You’ll take ownership of firmware development for a new class of insulin delivery technology, working at the intersection of engineering, quality, and regulatory compliance. This role is ideal for someone who thrives in structured environments, enjoys collaborating with cross‑functional teams, and wants their work to have … Leading development of safety‑critical firmware for insulin pump systems Defining and improving firmware lifecycle processes, documentation, and audit readiness Working closely with Quality, Regulatory, and Systems Engineering teams Ensuring compliance with IEC 62304, ISO 13485, and medical device development standards Contributing to architecture, design reviews, risk management ...