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Medical Affairs Director | Johnson and Johnson| MedTech|UK

The Medical Affairs Director UK is a strategic leader responsible for shaping commercial strategy and driving innovation by leveraging deep surgical expertise and insights into the local healthcare ecosystem. Key responsibilities include stakeholder engagement, evidence strategy, and scientific leadership to support regulatory approval, market access, and clinical adoption of J&J MedTech products.

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

Medical Affairs Director | Johnson and Johnson| MedTech|UK

The Medical Affairs Director UK is a strategic leader responsible for shaping commercial strategy and driving innovation by leveraging deep surgical expertise and insights into the local healthcare ecosystem. Key responsibilities include stakeholder engagement, evidence strategy, and scientific leadership to support regulatory approval, market access, and clinical adoption of J&J MedTech products.

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

Senior Clinical Trial Leader

The Senior Clinical Trial Leader will support the planning and execution of clinical trials for medical devices, working closely with cross-functional teams, clinical sites, and external partners. The role involves ensuring quality and compliance while contributing to innovative medical device development that improves patient outcomes.

Johnson & Johnson MedTech
On-site Permanent

Senior Specialist, Clinical Risk Management

The Senior Specialist, Clinical Risk Management, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Responsibilities include active participation in study activities, regular risk reviews, maintaining clinical quality plans, and communicating risk updates to stakeholders.

Johnson & Johnson MedTech United States
On-site Permanent

Senior Specialist, Clinical Risk Management

The Senior Specialist, Clinical Risk Management, works closely 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 risk management activities, maintain clinical quality plans, and communicate risk updates to stakeholders through regular reviews and governance meetings.

Johnson & Johnson MedTech
On-site Permanent

Senior Specialist, Clinical Risk Management

The Senior Specialist, Clinical Risk Management, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Key responsibilities include active participation in study activities, regular risk reviews, maintaining clinical quality plans, and facilitating risk updates to R&D colleagues.

Johnson & Johnson MedTech
On-site Permanent

Senior Specialist, Clinical Risk Management

The Senior Specialist, Clinical Risk Management, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Responsibilities include active participation in study activities, maintaining clinical quality plans, and facilitating regular risk reviews and updates.

Johnson & Johnson MedTech
On-site Permanent

Senior Specialist, Clinical Risk Management

The Senior Specialist, Clinical Risk Management, collaborates with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Key responsibilities include participating in risk assessments, maintaining clinical quality plans, and communicating risk updates to R&D colleagues through regular review cycles.

Johnson & Johnson MedTech Belgium
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

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

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

Director, 3rd Party RM. Program (BPO)

The Director, 3rd Party RM Program provides strategic leadership for an enterprise-wide third-party risk management program, focusing on anti-bribery and anti-corruption risks. Key responsibilities include setting global standards, developing risk assessment frameworks, overseeing due diligence processes, and partnering with Legal and IT to implement technology solutions.

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

Senior Manager Clinical Operations - Early Development

This role involves managing and shaping the Early Development & Clinical Pharmacology (ED&CP) structure, overseeing trial operations, and ensuring compliance with regulations. Responsibilities include line management, resource allocation, and driving process improvements. The position is hybrid, with 3 days onsite and 2 days remote.

Johnson & Johnson MedTech High Wycombe, United Kingdom
Hybrid 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

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