Future Tech Jobs
Future Tech Jobs
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through...
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through...
This role involves leading end-to-end operational transformation programs within healthcare systems across EurAsia, working closely with hospital leaders and internal teams to turn strategic insights into practical, sustainable improvements. The Principal Consultant will drive performance optimization in areas like care pathways, operations, and service delivery, using a blend of consulting expertise and hands-on execution. The position emphasizes scalable solutions, knowledge sharing, and shaping offerings within a remote-based, travel-inclusive model.
This role involves developing and implementing sales and call plans for hospitals, providing technical expertise through sales presentations and product demonstrations, and offering training and support to medical professionals. The position focuses on maintaining and growing business in the Cardiac Ablation Solutions (CAS) market, particularly in Electrophysiology (EP).
As a Surgical Training Technician, you will prepare and maintain laboratory spaces for surgical education, support live training sessions, and ensure compliance with regulatory frameworks. You will work closely with Medical Education, Marketing, and R&D teams, managing stock levels and maintaining inventory systems.
The Operational Quality 1 role involves maintaining high standards of quality and compliance in the manufacturing process. Responsibilities include reviewing and releasing product documentation, managing non-conformances, and supporting quality audits. The role also involves leading investigations and dispositions of defective materials and ensuring compliance with quality management systems.
This role involves leading the scientific safety assessment of pharmaceutical products across development and post-marketing stages, with responsibility for analyzing complex medical data, supporting global safety strategy, and contributing to regulatory compliance. The scientist will lead safety evaluations, guide cross-functional teams, and ensure high-quality reporting while acting as a subject matter expert during audits and inspections. Innovation in data presentation and process improvement is emphasized within a hybrid work environment.
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 position supports inspection readiness, drives risk-based oversight, and collaborates with cross-functional teams to implement effective quality strategies and corrective actions.
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 position drives risk-based oversight, supports inspection readiness, and provides expert guidance on quality issues and corrective actions within a global, cross-functional environment.
This role leads clinical risk management across therapeutic areas, ensuring trial data integrity, patient safety, and regulatory compliance. The Associate Director drives risk-based oversight, inspection readiness, and quality assurance for clinical trials, working closely with global teams to identify, assess, and mitigate risks. They also support audits, develop quality strategies, and provide expert guidance on GCP and regulatory standards.
This role involves leading clinical risk management activities across therapeutic areas, ensuring trial data integrity, patient safety, and regulatory compliance. The Associate Director drives risk-based oversight, supports inspection readiness, and advises on quality issues and corrective actions within global clinical trials. They collaborate with cross-functional teams to implement robust quality systems and continuous improvement in clinical development.
This role involves leading clinical risk management across therapeutic areas in Johnson & Johnson's R&D Quality team. The individual will identify, assess, and mitigate quality risks impacting clinical trial data integrity, patient safety, and regulatory compliance. They will drive risk-based oversight, support inspection readiness, lead quality investigations, and provide expert guidance on GCP and regulatory standards across global trial teams.
This role involves leading clinical risk management across therapeutic areas in Johnson & Johnson’s R&D organization, focusing on ensuring data integrity, patient safety, and regulatory compliance in clinical trials. The Associate Director will drive risk-based oversight, support inspection readiness, and provide expert guidance on quality issues and corrective actions. They will collaborate with cross-functional teams to identify, assess, and mitigate risks throughout the trial lifecycle.
This role involves leading clinical risk management across multiple therapeutic areas, focusing on ensuring trial data integrity, patient safety, and regulatory compliance. The individual will drive risk-based oversight, support inspection readiness, and guide cross-functional teams in implementing quality strategies throughout clinical development. A key aspect is providing expert advice on quality issues and leading continuous improvement in clinical trial quality systems.
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.
