Latest quality assurance Jobs

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

Product Portfolio Marketing Specialist

This role involves shaping the competitive position of bladder and bowel neurostimulation therapies internationally. Responsibilities include leading product launches, developing marketing strategies, and collaborating with cross-functional teams to ensure successful market penetration and growth.

Medtronic

Remote Permanent

Product Portfolio Marketing Specialist

In this role, you will shape the competitive positioning of bladder and bowel neurostimulation therapies internationally, leading product launches, marketing strategies, and cross-functional collaboration to drive growth and commercial success. You will work closely with sales, market development, and global marketing teams to ensure effective go-to-market execution and customer engagement.

Medtronic

Remote Permanent

Senior Analytical Monitor

The Senior Analytical Monitor role involves conducting analytical monitoring activities for multiple clinical trials, ensuring compliance with regulations and company policies. Responsibilities include performing regular reviews, detecting issues early, and collaborating with Site Managers and Central Monitoring Managers to improve data reliability and site satisfaction.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Senior Clinical Trial Leader

The Senior Clinical Trial Leader role involves planning and executing clinical trials for innovative medical devices, working closely with cross-functional teams, clinical sites, and external partners. The position focuses on advancing clinical research and ensuring quality and compliance in the development of medical devices that improve patient outcomes.

Johnson & Johnson MedTech Leeds, United Kingdom

On-site Permanent

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

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 on specific projects under supervision.

Johnson & Johnson MedTech Canada

Remote Permanent

Medical Writer II, Oncology

The Medical Writer II, Oncology role involves writing and coordinating clinical and regulatory documents, such as Phase 1-3 protocols, CSRs, and IB updates. You will work in a team environment, applying internal standards and regulatory guidelines, and participate in process working groups to support the development of oncology treatments.

Johnson & Johnson MedTech Switzerland

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, clinical study reports, and initial IBs. 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 Belgium

On-site Permanent

Product Manager - EMEA

As a Product Manager, you will lead cross-functional teams to develop innovative AI and digital solutions for the orthopedics supply chain. You will collaborate with business partners to implement data-driven decisions, drive growth, and streamline processes in a dynamic and complex environment.

Johnson & Johnson MedTech Ireland

On-site Permanent

Manager, Medical Writing, Immunology

The Manager, Medical Writing, Immunology role involves preparing and finalizing clinical documents, leading team projects, and guiding cross-functional team members on processes and best practices. The position focuses on the Immunology therapeutic area and supports the development of transformational medicines for immunological disorders.

Johnson & Johnson MedTech Switzerland

On-site Permanent

Manager, Medical Writing, Immunology

The Manager, Medical Writing, Immunology role involves preparing and finalizing clinical documents, leading cross-functional teams, and guiding team members on processes and best practices. The position focuses on the Immunology therapeutic area, with responsibilities including content and scientific strategy, project management, and process improvements.

Johnson & Johnson MedTech Canada

Remote Permanent

Manager, Medical Writing, Immunology

This role involves preparing and finalizing clinical documents for the Immunology therapeutic area, leading cross-functional teams, and guiding team members on processes and best practices. The Manager will work with a high level of independence, take a lead role in content and scientific strategy, and proactively recommend process improvements.

Johnson & Johnson MedTech Belgium

On-site Permanent