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 providing clinical expertise and education in complex wound care across the Yorkshire and Humber region, supporting healthcare professionals in the community to improve patient outcomes. The specialist will deliver hands-on training, build relationships with clinicians, and ensure effective use of advanced wound management therapies. It combines clinical knowledge with field-based sales and advocacy within a supportive, patient-focused environment.
Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.We are currently searching for aSenior Productivity & Cost Optimisation Engineer.The Senior Productivity & Cost Optimisation Engineer is a strategic, technically grounded professional responsible for identifying,...
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...
The UK Pricing & Contracting Systems Specialist role involves managing the development and coordination of offers, contracts, and related analytics. The position requires strong business acumen, advanced analytics skills, and the ability to guide team members to ensure accuracy and quality in contract management and offer development.
This role involves managing and improving content compliance and copy review processes across EMEA markets, ensuring promotional materials meet regulatory and procedural standards. The specialist supports audit readiness, drives process efficiency, and contributes to digital innovation using AI and automation tools. Working in a multilingual, matrixed environment, they provide guidance to submitters and maintain high-quality, compliant content workflows.
This role involves providing medical expertise in the evaluation of safety data from adverse event reports, clinical studies, and literature to support pharmacovigilance activities. The physician will assess case-level and aggregate safety data, identify emerging risks, and contribute to safety reviews and risk management plans. Work includes cross-functional collaboration, signal detection, and ensuring compliance with regulatory standards in a global healthcare environment.
This role involves leading the safety assessment and risk management of immunology drugs in clinical development and on the market, providing medical oversight on safety data, and contributing to regulatory submissions. The Medical Safety Officer collaborates with cross-functional teams to evaluate drug safety profiles, design risk mitigation strategies, and communicate findings to health authorities and internal leadership. It is a strategic position requiring strong medical, regulatory, and communication expertise in pharmacovigilance.
This role involves leading the medical safety assessment of pharmaceutical products throughout their lifecycle, with a focus on proactive safety surveillance, risk management, and benefit-risk evaluation. The Medical Safety Officer provides expert medical input into clinical development and regulatory documentation, leads cross-functional Safety Management Teams, and ensures compliance with global pharmacovigilance standards. Key responsibilities include signal detection, risk mitigation strategy design, and communication of safety findings to internal leadership and health authorities.
This role involves developing and executing regulatory strategies for solid tumour products across Europe, the Middle East, and Africa, with a focus on clinical trial applications, marketing authorisation submissions, and lifecycle management. The professional will collaborate with cross-functional teams and regulatory agencies, ensuring compliance and timely approvals for oncology pharmaceuticals. Work includes drafting submissions, responding to health authority queries, and supporting scientific advice procedures.
This role involves developing and executing regulatory strategies for solid tumour pharmaceutical products across Europe, the Middle East, and Africa. The professional will lead submissions to health authorities, support clinical trial applications, marketing authorizations, and lifecycle management, while collaborating with cross-functional teams and regulatory agencies. Expertise in EMA procedures and oncology regulations is central to ensuring compliance and timely product commercialization.
This role involves developing and executing regulatory strategies for pharmaceutical products in the EMEA region, with a focus on oncology. The professional will support submissions to health authorities, including clinical trial applications and marketing authorization dossiers, while collaborating with cross-functional teams and regulatory agencies. Key responsibilities span pre-authorization, authorization, and post-approval lifecycle management across solid tumour therapies.
This role involves managing and improving content compliance and copy review processes across EMEA markets for MedTech promotional materials. The specialist ensures regulatory adherence, supports audit readiness, and drives process efficiency through digital tools, AI, and automation. They provide guidance to submitters, maintain documentation, and contribute to system enhancements in a multilingual, cross-regional environment.
This role involves leading the safety assessment and risk management of Innovative Medicine products within the Immunology therapeutic area. The Medical Safety Officer provides medical expertise on safety data, leads cross-functional teams, and ensures compliance with global regulations through activities like signal detection, risk mitigation, and regulatory reporting. The position plays a key part in shaping safety strategy across clinical development and post-marketing phases.
