Latest Pharmaceuticals Jobs

Field Service Engineer, Medical Diagnostic Systems

This role involves installing, servicing, and repairing advanced medical diagnostic analysers used in NHS and private pathology laboratories. The engineer will conduct preventative maintenance, respond to breakdowns, and provide technical support on-site, ensuring minimal downtime for critical healthcare equipment. The position offers comprehensive training and supports a diverse range of high-value scientific instrumentation.

TRS Consulting Cheltenham, Gloucestershire, United Kingdom £45,000 – £48,000 pa

Hybrid Permanent

Field Service Engineer, Medical Diagnostic Systems

The role involves servicing and repairing advanced medical diagnostic systems used in pathology and clinical laboratories. The engineer will visit customer sites to perform maintenance, troubleshoot issues, and deliver technical solutions. Full product training is provided, and the position supports a globally recognised healthcare technology provider.

TRS Consulting Worcester, Worcestershire, United Kingdom £45,000 – £48,000 pa

Hybrid Permanent

Manager, Trial Delivery Management

This role involves managing the execution of clinical trials at the study level, including oversight of trial documentation, vendor management, and regional coordination of trial activities. The Manager ensures alignment of feasibility strategies, conducts risk reviews, and supports compound training in collaboration with clinical teams. They also contribute to operational strategy, mentor team members, and support compliance during health authority inspections.

Johnson & Johnson MedTech

Hybrid Permanent

Manager, Trial Delivery Management

Manages the execution of clinical trial activities, including oversight of trial-specific documentation, vendor management, and regional operational delivery. Coordinates feasibility strategies, risk assessments, and compliance across global teams while supporting training and process improvements. Provides leadership in a matrixed environment and mentors team members in trial management functions.

Johnson & Johnson MedTech

Hybrid Permanent

Manager Regulatory Medical Writing X-TA

This role involves leading the preparation and finalization of clinical and regulatory documents within a global medical writing team, with a focus on cross-functional collaboration and scientific strategy. The individual will guide teams, ensure compliance with regulatory standards such as ICH, and mentor junior staff. Based in a hybrid work model, the position supports multiple therapeutic areas and drives process improvements in medical writing operations.

Johnson & Johnson MedTech €78,300 – €135,700 pa

Hybrid Permanent

Associate Director, Clinical Risk Management

This role involves leading clinical risk management across therapeutic areas, focusing on identifying, assessing, and mitigating quality risks in clinical trials to ensure patient safety, data integrity, and regulatory compliance. The individual will drive risk-based oversight, support inspection readiness, lead quality investigations, and provide expert guidance to cross-functional teams within a global R&D environment.

Johnson & Johnson MedTech Spain

Hybrid Permanent

Associate Director, Clinical Risk Management

This role involves leading clinical risk management across multiple therapeutic areas, focusing on identifying, assessing, and mitigating quality risks in clinical trials to ensure patient safety, data integrity, and regulatory compliance. The individual will drive risk-based oversight, support inspection readiness, lead quality investigations, and advise on CAPA plans in a global, cross-functional environment. Key activities include coaching teams, maintaining clinical quality plans, and contributing to governance forums to uphold high standards in clinical development.

Johnson & Johnson MedTech

Hybrid Permanent

Manager, Medical Writing, Immunology

Lead and manage the development of clinical and regulatory medical writing deliverables within the Immunology therapeutic area, providing scientific and strategic input across the product lifecycle. This role involves direct supervision of medical writers, mentoring junior staff, leading cross-functional writing teams, and ensuring compliance with regulatory standards. The position requires deep expertise in medical writing processes, ICH guidelines, and clinical documentation, with a strong emphasis on leadership, project management, and process improvement.

Johnson & Johnson MedTech

On-site Permanent

Manager, Medical Writing, Immunology

Lead and manage medical writing activities for immunology clinical documents, including planning, authoring, and mentoring junior staff. Guide cross-functional teams, ensure regulatory compliance, and drive process improvements in a global healthcare environment.

Johnson & Johnson MedTech Belgium

On-site Permanent

Manager, Medical Writing, Immunology

This role involves leading the development and finalization of clinical and regulatory documents within the Immunology therapeutic area, with a focus on scientific strategy, team leadership, and cross-functional collaboration. The manager will oversee medical writing projects from planning to delivery, mentor junior staff, and ensure compliance with regulatory standards such as ICH guidelines. The position also includes direct people management, process improvement, and coordination across global teams in a patient-centered innovation environment.

Johnson & Johnson MedTech Switzerland

On-site Permanent

Lead Analyst-Global Reporting

This role involves leading and coordinating transparency reporting across EMEA markets, ensuring compliance with regional and local regulations. The candidate will develop reporting frameworks, drive process improvements, and leverage automation and analytics to enhance data quality and operational efficiency. They will also act as a compliance advisor, translating regulatory changes into actionable processes while supporting governance, risk assessments, and stakeholder training.

Johnson & Johnson MedTech Switzerland

Hybrid Permanent

Associate Dir. Cross TA Risk Management

This role leads clinical risk management across therapeutic areas in J&J's R&D organization, focusing on ensuring data integrity, patient safety, and regulatory compliance in clinical trials. The individual will drive risk-based oversight, support inspection readiness, and provide expert guidance on quality issues and CAPA plans. The position operates in a global, cross-functional environment and contributes to shaping quality systems and processes across clinical development.

Johnson & Johnson MedTech United States US$122,000 – US$212,750 pa

Hybrid Permanent

Associate Dir. Cross TA Risk Management

This role involves leading clinical risk management across therapeutic areas, ensuring data integrity, patient safety, and regulatory compliance in global clinical trials. The Associate Director drives risk-based oversight, inspection readiness, and quality governance, working closely with cross-functional teams to identify, assess, and mitigate risks throughout trial lifecycles. They also support audits, inspections, and the development of corrective actions, contributing to a robust quality framework in R&D.

Johnson & Johnson MedTech US$122,000 – US$212,750 pa

Hybrid Permanent

Associate Dir. Cross TA Risk Management

This role involves leading clinical risk management across therapeutic areas, ensuring data integrity, patient safety, and regulatory compliance in global clinical trials. The Associate Director will drive risk-based oversight, inspection readiness, and quality investigations, while advising trial teams and collaborating with cross-functional stakeholders to maintain high standards in clinical research quality.

Johnson & Johnson MedTech US$122,000 – US$212,750 pa

Hybrid Permanent

Associate Dir. Cross TA Risk Management

This role involves leading clinical risk management across therapeutic areas, ensuring trial data integrity, patient safety, and regulatory compliance. The individual will drive risk-based oversight, develop Clinical Quality Plans, support inspection readiness, and advise on quality issues and CAPAs in a global, cross-functional environment.

Johnson & Johnson MedTech US$122,000 – US$212,750 pa

Hybrid Permanent