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...
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 the preparation and finalization of clinical and regulatory documents within a global medical writing team, with a focus on strategic content planning and cross-functional collaboration. The manager will oversee writing projects across multiple therapeutic areas, mentor junior staff, ensure compliance with regulatory standards, and contribute to process improvements. Based in High Wycombe with a hybrid working model, the position requires strong scientific communication, project leadership, and regulatory expertise.
Leads medical writing activities for clinical documents in the Immunology therapeutic area, providing scientific and strategic leadership. Manages a team of medical writers, mentors junior staff, and collaborates cross-functionally to ensure regulatory compliance and high-quality documentation. Works within a global regulatory environment, contributing to process improvements and departmental best practices.
This role involves leading the production of plain language summaries (PLS) for clinical trial results, ensuring scientific accuracy and compliance with regulatory standards while making content accessible to non-specialist audiences. The manager will oversee vendor performance, collaborate with cross-functional teams across therapeutic areas, and ensure adherence to health literacy principles and global disclosure requirements. Key responsibilities include maintaining robust PLS processes, addressing content issues, and supporting translation workflows.
This role leads the strategy and governance of Standard Operating Procedures (SOPs) for Medical and Scientific Affairs within DePuy Synthes, focusing on clinical research, Medical Affairs, and clinical evidence generation for orthopedic medical devices. The position ensures global regulatory compliance, drives SOP updates in response to evolving standards, and coordinates cross-functionally to maintain audit readiness and operational excellence across a highly regulated environment.
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 leads the design and execution of a global operational excellence framework across DePuy Synthes' supply chain and operations. The Director will establish performance standards, drive continuous improvement initiatives using Lean and Six Sigma methodologies, and embed a culture of data-driven decision-making across manufacturing, planning, procurement, and logistics functions. They will work cross-functionally to deliver measurable improvements in cost, service, quality, and working capital within a highly regulated MedTech environment.
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 the preparation and finalization of clinical and regulatory documents within a cross-functional environment, ensuring scientific accuracy and compliance with regulatory standards. The manager will guide teams, mentor junior staff, and drive process improvements in medical writing, with a strong focus on strategic planning and cross-departmental collaboration.
This role involves leading the preparation and finalization of clinical and regulatory documents within a cross-functional environment, providing scientific and strategic direction for medical writing teams. The manager will mentor junior staff, drive process improvements, and serve as the primary liaison between medical writing and clinical teams, ensuring compliance with regulatory standards across multiple therapeutic areas.
Leads and oversees the preparation of clinical and regulatory documents, providing scientific and strategic direction for medical writing teams. Champions document planning, ensures regulatory compliance, and mentors junior staff while collaborating across functions to deliver high-quality submissions. Focuses on process improvement and cross-functional alignment in a hybrid work environment.
This role involves leading the preparation and finalization of clinical and regulatory documents within Johnson & Johnson's MedTech division, supporting multiple therapeutic areas. The manager will lead writing teams, guide cross-functional colleagues, ensure compliance with regulatory standards such as ICH, and drive process improvements. A key focus is scientific strategy, project leadership, and mentoring junior staff in a hybrid work environment.
This role involves leading the preparation and finalization of clinical and regulatory documents across multiple therapeutic areas, with a focus on strategic input, project leadership, and compliance with global regulatory standards. The manager will lead writing teams, mentor junior staff, and collaborate cross-functionally to ensure high-quality submissions. They will also contribute to process improvements and maintain alignment with ICH and other regulatory guidelines.
