Medical Technology Jobs in Milton Keynes

Associate Director, Safety Analysis Scientist

This role involves leading scientific safety evaluations for pharmaceutical products across development and post-marketing stages, with a focus on analyzing complex medical data, shaping safety strategies, and supporting regulatory compliance. The scientist will serve as a subject matter expert, lead cross-functional safety reviews, contribute to key clinical documents, and drive innovation in safety analysis methodologies. Emphasis is placed on proactive risk assessment, collaboration with global teams, and ensuring high-quality, timely safety reporting.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Manager, Clinical Operations

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through...

Johnson & Johnson MedTech High Wycombe, United Kingdom

Development Scientist

The role involves working within the Sequencing Development Team to advance sequencing technologies. Responsibilities include conducting experiments, analyzing data, and contributing to the development of new sequencing methods and products.

Oxford Nanopore Technologies Oxford, United Kingdom

On-site Permanent

Senior Director, Product Management - Sequencing Systems

The Senior Director of Product Management will lead the strategy and lifecycle management of sequencing systems, working closely with R&D, Product Development, Commercial, Marketing, Operations, and Regulatory teams to ensure products deliver customer value and align with company strategy.

Oxford Nanopore Technologies Oxford, United Kingdom

On-site Permanent

Full Stack Developer

The Full Stack Developer role involves hands-on software engineering, focusing on building and maintaining high-quality applications and solutions across OrganOx's digital platforms. Responsibilities include coding, API design, database management, DevOps, and collaboration with internal and external teams to support regulated medical device and data solutions.

OrganOx Oxford, United Kingdom

On-site Permanent

Process Engineer, Validation

The Process Engineer, Validation leads and executes validation activities for new product ranges and changes to existing medical devices. They ensure all manufacturing processes, equipment, and test methods meet internal and external regulatory standards, working closely with cross-functional teams and external partners. The role involves developing validation strategies, authoring protocols, conducting risk assessments, and supporting regulatory submissions.

OrganOx Oxford, United Kingdom

On-site Permanent

Experienced Stat Programmer

The Experienced Statistical Programmer is responsible for developing, verifying, and documenting code for clinical data analysis and reporting. They work on tasks of medium to high complexity, ensuring quality and timeliness, and collaborate with cross-functional teams to achieve project goals.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site Permanent

Specialist, Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, works with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. They actively participate in study activities, maintain clinical quality plans, and communicate risk updates to R&D colleagues through regular review cycles.

Johnson & Johnson MedTech High Wycombe, United Kingdom

On-site Permanent