5 of 5 Regulatory Compliance Jobs in Wilmslow

Project Manager

Location
Wilmslow, England, United Kingdom
coordination of complex IVD development programmes, bringing together diverse teams to deliver innovative LC-MS diagnostic solutions that meet the highest standards of quality, regulatory compliance, and commercial success. This is an exciting opportunity to contribute to products that have a meaningful impact on patient care while developing … link up with risk management approach. Manage project execution to meet cost, schedule, and performance targets Cross-Functional Coordination Collaborate with R&D, Clinical, Regulatory Affairs, Quality, Supply Chain, and Marketing Coordinate meetings, actions, and follow-ups across project teams Support clear communication of project updates and status Regulatory ...

Senior Principal Test Engineer - Clinical Software & LC-MS

Location
Wilmslow, England, United Kingdom
lead testing, verification, and validation of software-driven clinical systems. You will collaborate across software, hardware and quality teams to ensure reliability, cybersecurity, and regulatory compliance for LC-MS instrumentation and associated workflows. The role focuses on software-controlled analytical platforms with opportunities to shape testing strategy, mentor ...

IVD Product Development Project Manager

Location
Wilmslow, England, United Kingdom
drive end-to-end workstreams across assays, instruments and software, coordinating cross-functional teams to deliver on time and within budget. The role emphasizes regulatory compliance, design control processes, risk management and continuous improvement. Travel up to 20% to Waters offices is expected, with a strong focus ...

Principal IVD Engineer, Clinical Software

Location
Wilmslow, England, United Kingdom
technical authority for complex clinical and diagnostic software systems. Lead the evaluation and design of software architectures that balance performance, maintainability, scalability, security, and regulatory compliance. Guide engineering teams in adopting robust development practices, including software design, verification, validation, traceability, cybersecurity, and risk management. Partner with Software, Systems, Quality … Regulatory, Scientific, and Product Management teams throughout the product lifecycle. Contribute technical expertise to product planning, technology roadmaps, and architectural governance activities. Champion secure-by-design principles and help ensure cybersecurity considerations are incorporated throughout the software lifecycle. Evaluate emerging technologies, development approaches, industry trends, and evolving regulatory ...

Principal Test Engineer, Clinical Software

Location
Wilmslow, England, United Kingdom
systems engineers, hardware engineers, product owners, and quality teams, you will help ensure our products meet the highest standards of reliability, performance, cybersecurity, and regulatory compliance. This role has a particular focus on the testing and verification of software-controlled analytical instrumentation and integrated LC-MS systems. … software, or integrated laboratory informatics systems. Experience working in clinical diagnostics, healthcare, medical device, IVD, pharmaceutical, or laboratory instrumentation environments. Knowledge of validation and compliance activities for regulated products. Experience with automated testing frameworks, test automation tools, and data-driven testing approaches. Understanding of cybersecurity testing concepts and secure ...