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Launch Excellence Lead Velys Trauma & Data Products

The Launch Excellence Lead for Velys Trauma & Data Products is responsible for managing complex projects and processes, coordinating cross-functional teams, and driving process development and simplification. This role ensures the successful implementation of Velys Digital and Capital technologies, supports data-driven decision-making, and aligns project timelines across regional and functional teams.

Johnson & Johnson MedTech Leeds, United Kingdom
On-site Permanent

Engineering Technician

The Engineering Technician role involves maintaining, fault-finding, and repairing CNC machines in a regulated medical device production environment. Responsibilities include performing preventive maintenance, diagnosing issues, and supporting machine setup and qualification activities. The role also focuses on continuous improvement to increase equipment uptime and process yield.

Johnson & Johnson MedTech Leeds, United Kingdom
On-site Permanent

Post Doctoral Researcher, Evaluation & Standards in Clinical Operations

This role involves developing evaluation frameworks and rubrics for AI agents in clinical operations and global development. Responsibilities include designing quality dimensions, running human evaluation protocols, and building benchmark datasets. The position requires a strong understanding of clinical operations, regulatory documentation, and AI systems.

Johnson & Johnson MedTech High Wycombe, United Kingdom
On-site Permanent

Clinical Trial Leader

The Clinical Trial Leader role involves supporting the planning and execution of clinical trials for medical devices, working closely with cross-functional teams, clinical sites, and external partners. The position focuses on ensuring trials are conducted with quality and compliance, contributing to the development of innovative medical devices that improve patient outcomes.

Johnson & Johnson MedTech Leeds, United Kingdom
On-site Permanent

Associate Director, RA UK & Ireland

The role involves leading and overseeing regulatory affairs activities for the UK market, ensuring compliance with UK and EU regulations, and managing regulatory risk. The Associate Director will partner with various teams to support product registrations, lifecycle management, and business initiatives, while also leading the UKCA marking strategy and coaching regulatory team members.

Johnson & Johnson MedTech Leeds, United Kingdom
On-site Permanent

EMEA HEMA Associate Manager

The EMEA HEMA Associate Manager supports the regional development and execution of Health Economics & Market Access activities, working closely with country HEMA Leads. Responsibilities include coordinating EMEA initiatives, generating evidence, developing value tools, and ensuring compliance with governance standards.

Johnson & Johnson MedTech Leeds, United Kingdom
On-site Permanent

D&A and Master Data Specialist

The role involves managing the accuracy and consistency of master data across various commercial systems, implementing data governance practices, and ensuring compliance with regulations like GDPR. Responsibilities include collaborating with internal stakeholders, developing data management strategies, and utilizing tools like Power BI and Excel to create analytical reports and dashboards.

Johnson & Johnson MedTech Leeds, United Kingdom
On-site Permanent

HEMA Lead UK

The HEMA Lead UK is responsible for shaping and executing health economics and market access strategies for DePuy Synthes in the United Kingdom. Key responsibilities include leading payer and HTA engagement, developing value dossiers, and ensuring successful reimbursement and adoption of innovative orthopaedic solutions. The role involves cross-functional collaboration and compliance with regulatory requirements.

Johnson & Johnson MedTech Leeds, United Kingdom
On-site Permanent

Sr. Source Reg Compliance Specialist

The Sr. Source Regulatory Compliance Specialist is responsible for ensuring suppliers and externally provided processes comply with regulatory requirements and quality standards. Key responsibilities include executing supplier audits, supporting compliance oversight, and maintaining documentation. The role involves close collaboration with Quality, Regulatory Affairs, Supply Chain, and Procurement teams to maintain product quality and supply continuity.

Johnson & Johnson MedTech Leeds, United Kingdom
On-site Permanent

Senior Director, Data, Advanced Analytics & AI – Innovative Medicine (EMEA)

This role involves defining and executing an AI-first, product-centric data strategy for Johnson & Johnson's Innovative Medicine division in EMEA. Responsibilities include leading end-to-end data and AI capabilities, ensuring responsible deployment, and building robust data ecosystems. The role also focuses on translating business priorities into scalable outcomes and fostering innovation within cross-functional teams.

Johnson & Johnson MedTech Spain
On-site Permanent

VELYS Trauma Marketing Manager

The VELYS Trauma Marketing Manager will lead the launch and establishment of the new VELYS Trauma system within the DPS International business and Trauma Platforms. Key responsibilities include developing and executing international strategies, partnering with cross-functional teams, and ensuring market access and clinical evidence strategies are in place.

Johnson & Johnson MedTech Leeds, 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

Director, Major Markets Europe & Canada

The Director, Major Markets Europe & Canada, provides strategic regulatory leadership across key European and Canadian markets. This role ensures compliance with local and regional regulatory requirements, manages regulatory risk, and supports business growth in highly regulated markets. Key responsibilities include leading regulatory affairs strategy, ensuring compliance, and partnering with cross-functional teams to manage product registrations and lifecycle management.

Johnson & Johnson MedTech Leeds, United Kingdom
Hybrid Permanent

Director, Clinical Risk Management Post Approval Delivery Unit

This role involves overseeing clinical risk management for post-approval clinical trials, ensuring data integrity, patient safety, and compliance with regulatory requirements. Responsibilities include leading a team of CRM Representatives, conducting risk assessments, and developing mitigation strategies.

Johnson & Johnson MedTech High Wycombe, United Kingdom
On-site Permanent

Associate Director, Regulatory Policy

The Associate Director, Regulatory Policy, provides leadership in regulatory compliance and policy, ensuring alignment with global and regional requirements. Key responsibilities include interpreting regulatory policies, developing internal guidelines, and supporting cross-functional teams to manage regulatory risks and enable informed decision-making.

Johnson & Johnson MedTech Leeds, United Kingdom
On-site Permanent

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