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Hips Lifecycle Management Leader - EMEA

The Lifecycle Management Leader for Hips will oversee the lifecycle management of hip-related medical devices, ensuring the development and execution of strategic projects. This role involves collaborating with cross-functional teams to drive innovation, improve product quality, and enhance patient outcomes in orthopaedic treatments.

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

Hips Lifecycle Management Leader

The Hips Lifecycle Management Leader role involves leading the lifecycle management of hip joint products within the MedTech Orthopaedics business. Responsibilities include strategic planning, product development, and collaboration with cross-functional teams to drive innovation and improve patient outcomes.

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

Specialist Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, 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 review cycles.

Johnson & Johnson MedTech United States
On-site Permanent

Specialist Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, 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, maintaining clinical quality plans, and facilitating regular risk reviews and updates.

Johnson & Johnson MedTech
On-site Permanent

Specialist Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, 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 coordinating data-driven risk oversight, maintaining clinical quality plans, and communicating risk updates to stakeholders through regular review cycles.

Johnson & Johnson MedTech
On-site Permanent

Specialist, Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, 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 coordinating data-driven risk oversight, maintaining clinical quality plans, and communicating risk updates to R&D colleagues through regular review cycles.

Johnson & Johnson MedTech Belgium
On-site Permanent

EMEA HEMA Associate Manager

The EMEA HEMA Associate Manager supports the regional development and execution of Health Economics & Market Access activities across EMEA. Key responsibilities include coordinating EMEA initiatives, generating evidence, developing value tools, and ensuring compliance with governance and regulatory standards.

Johnson & Johnson MedTech Switzerland
On-site Permanent

EMEA HEMA Associate Manager

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

Johnson & Johnson MedTech
On-site Permanent

EMEA HEMA Associate Manager

The EMEA HEMA Associate Manager supports the development and execution of Health Economics & Market Access activities across EMEA, 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
On-site Permanent

EMEA HEMA Associate Manager

The EMEA HEMA Associate Manager supports the regional development and execution of Health Economics & Market Access activities across EMEA. Key responsibilities include coordinating EMEA initiatives, generating evidence, developing value tools, and ensuring compliance with regulatory standards.

Johnson & Johnson MedTech
On-site Permanent

D&A and Master Data Specialist

The role involves maintaining and ensuring the accuracy of master data across multiple platforms, implementing data governance strategies, and collaborating with various departments to enhance data processes. The position also includes developing analytical reports and supporting the implementation of new MDM systems.

Johnson & Johnson MedTech
On-site Permanent

D&A and Master Data Specialist

This role involves maintaining and ensuring the accuracy of master data across multiple platforms, implementing data governance practices, and collaborating with various departments to enhance data processes. The position also includes developing analytical reports and supporting the implementation of new MDM systems.

Johnson & Johnson MedTech
On-site Permanent

Principal Portfolio Lead Clin Prog

This role involves formulating and executing the clinical programming strategy for a portfolio of medium to high complexity clinical trials. Responsibilities include planning, resource allocation, cross-functional collaboration, and ensuring compliance with quality and regulatory standards.

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

Medical Writer II, Oncology

This role involves writing and coordinating clinical and regulatory documents for oncology treatments, including Phase 1-3 protocols, CSRs, and IB updates. The Medical Writer II will work in a team environment, applying internal standards and regulatory guidelines, and may lead writing projects under supervision.

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

Manager, Safety Analysis Scientist

The Manager, Safety Analysis Scientist role involves leading the safety assessment of assigned products, preparing scientific safety analyses, and collaborating with cross-functional teams to ensure regulatory compliance. The role requires in-depth product knowledge, mentoring team members, and supporting safety management teams.

Johnson & Johnson MedTech High Wycombe, United Kingdom
Hybrid Permanent

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