Latest regulatory affairs specialist Jobs

Sr Director, C&SP - NS and Cardio-Pulmonary

The Senior Director, C&SP - Neuroscience & Cardiopulmonary will lead the strategic and operational aspects of clinical and statistical programming. This role involves shaping the long-term vision, guiding organizational evolution, and ensuring flawless execution across major therapeutic and regional portfolios. The position requires strong leadership skills to inspire and develop a global team, drive technical innovation, and collaborate with cross-functional stakeholders to deliver clinical evidence to global health authorities.

Johnson & Johnson MedTech Switzerland

Hybrid Permanent

Sr Director, C&SP - NS and Cardio-Pulmonary

The Senior Director, C&SP - Neuroscience & Cardio role involves leading a large, global team in Clinical & Statistical Programming, shaping the long-term strategy, and ensuring operational excellence across major therapeutic and regional portfolios. Responsibilities include guiding organizational evolution, making strategic decisions, and fostering collaboration across various functions to deliver clinical evidence to global health authorities.

Johnson & Johnson MedTech

Hybrid Permanent

Product Manager

The Product Manager will join a dynamic AI & Digital team focused on transforming the orthopaedics supply chain with innovative, scalable AI and digital solutions. The role involves strong organizational engagement, cross-functional collaboration, and implementing data-driven solutions to meet the growing demand for personalized care in the medical device industry.

Johnson & Johnson MedTech Leeds, United Kingdom

On-site Permanent

Hips Lifecycle Management Leader - EMEA

The Lifecycle Management Leader for Hips will orchestrate projects across the Hips Value Stream, focusing on innovation and continuous improvement in orthopaedic solutions. This role involves collaborating with cross-functional teams to drive the development and lifecycle management of hip-related medical devices, ensuring they meet clinical and economic standards.

Johnson & Johnson MedTech

On-site Permanent

Hips Lifecycle Management Leader

The Hips Lifecycle Management Leader role involves leading the lifecycle management of hip orthopaedic products, driving innovation and ensuring the delivery of high-quality, less invasive, and personalized treatments. The role is part of a global team focused on advancing orthopaedic solutions and improving patient outcomes.

Johnson & Johnson MedTech United States

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 ensuring the delivery of innovative and personalized treatments. The role is part of a global team focused on advancing orthopaedic solutions and improving patient outcomes.

Johnson & Johnson MedTech

On-site Permanent

Hips Lifecycle Management Leader

The Hips Lifecycle Management Leader role involves managing the lifecycle of hip joint products within the MedTech Orthopaedics business. Responsibilities include overseeing product development, innovation, and market strategies to ensure the delivery of advanced, less invasive, and personalized treatments. The role is part of a global team focused on improving patient outcomes and expanding the possibilities of orthopaedic care.

Johnson & Johnson MedTech

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 ensuring the delivery of innovative and high-quality orthopaedic solutions.

Johnson & Johnson MedTech

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

On-site 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

Experienced Clin Programmer

The Experienced Clinical Programmer is responsible for overseeing or developing complex clinical data management activities, including data model specifications, data stream integrations, and transformation of source data to internal models. They create and execute edit check programs, listings, and reports to ensure data quality and compliance, and may lead in process and tool improvements.

Johnson & Johnson MedTech High Wycombe, 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 across EMEA. Key responsibilities include coordinating EMEA initiatives, supporting evidence generation, and ensuring consistent market access strategies across multiple countries.

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. 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