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...
This role involves driving the commercial success of the Single Shot electrophysiology portfolio in EMEA, including market execution, launch support, customer engagement, and competitive response. You will work closely with cross-functional teams to ensure consistent and scalable portfolio adoption and performance tracking.
As an Orthopaedics Product Management Specialist, you will develop and execute product strategies for the Primary Knees segment, manage product launches, and collaborate with cross-functional teams. You will also lead surgeon consultant relationships, create marketing content, and maintain market knowledge through research and KOL engagement.
This role involves shaping the competitive landscape for bladder and bowel neurostimulation therapies internationally. You will lead product launches, develop marketing strategies, and collaborate with cross-functional teams to ensure successful market penetration and growth. The position requires a strong background in medical device marketing and the ability to work in a fast-paced, international environment.
This role involves shaping the competitive position of bladder and bowel neurostimulation therapies internationally. You will lead product launches, develop marketing strategies, and collaborate with cross-functional teams to drive growth and deliver measurable commercial results in a fast-evolving market.
This role involves managing key orthopaedic accounts across a defined UK territory, focusing on strategic planning, customer engagement, and revenue growth. The Account Manager will work closely with NHS stakeholders and internal teams to promote Smith & Nephew’s orthopaedic products, using CRM data and market insights to drive adoption. It’s a field-based position requiring frequent travel and relationship-building in clinical and procurement settings.
This role involves maintaining and improving a Quality Management System in a regulated medical device environment, with a focus on ISO13485 compliance, technical documentation, internal audits, and managing non-conformities and CAPAs. The specialist will ensure product literature meets regulatory standards and will act as a key contact during external audits, working closely with senior management and consultants.
Manages the preparation and delivery of regulatory submissions to health authorities across multiple markets, coordinating timelines, translations, and document builds. Acts as a subject matter expert on dossier types and eCTD standards while mentoring colleagues and resolving submission-related issues. Focuses on improving efficiency through reuse of submission content across regions.
This role involves leading Quality Assurance for new product introductions across a global network of external manufacturers. The specialist ensures compliance with GMP and regulatory standards during technology transfers, supports clinical trial manufacturing, and acts as the QA interface during audits and inspections. The position requires close collaboration with cross-functional teams and regular engagement with Contract Manufacturing Organizations.
This role involves maintaining regulatory compliance for medical devices by managing technical documentation, product registrations, and post-market surveillance activities. The specialist will work independently in an SME setting, ensuring adherence to UK and EU regulations including MDR, MDD, and UKCA. Responsibilities include updating clinical evaluations, supporting audits, and managing documentation with a focus on accuracy and efficiency.
This role involves supporting quality assurance and regulatory affairs activities within a medical devices R&D environment, ensuring compliance with ISO 13485, FDA 510(k), and 21 CFR Part 820 standards. The assistant will collaborate closely with R&D teams, providing guidance on regulatory requirements during product development and improvement. The position plays a key part in maintaining quality management systems and enabling the delivery of innovative, life-improving medical technologies.
This role involves monitoring and evaluating the safety profiles of medicines, particularly HIV treatments, across development and post-marketing stages. The Clinical Safety Scientist will conduct signal detection, analyse safety data, contribute to risk management plans, and support regulatory documentation. Close collaboration with safety physicians is required for benefit-risk assessments and compliance with global pharmacovigilance standards.
This role involves leading the end-to-end development of advanced medical and scientific devices within an ISO 13485-regulated environment. The Chief Mechanical Engineer will oversee multidisciplinary teams, manage technical and commercial aspects of projects, and contribute to innovation and thought leadership. The position emphasizes technical leadership, client engagement, and delivery of high-impact engineering solutions in a consultancy setting.
Job Description SummaryThis role provides regulatory strategy and direction to the business regarding healthcare industry regulatory requirements for product launch, premarket submissions/registrations and postmarket compliance, working closely with healthcare regulatory bodies globally. Interprets simple internal and external business challenges and...
Job Advertisement: Sales Specialist (West Midlands)Are you ready to make a significant impact in the healthcare sector? Join our client's Core Lab Sales Team as a Sales Specialist, where you will play a vital role in delivering innovative diagnostic solutions...
