Future Tech Jobs
Future Tech Jobs
CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means...
The Director, Biostatistics, leads the full scope of statistical contribution to a clinical development program, including life cycle management. The AD provides for statistical excellence in clinical development plans, trial planning, data analysis, interpretation and reporting, and regulatory interactions and...
An exciting hybrid working opportunity has arisen for an experienced Bioinformatician to join a high-impact team supporting clinical-stage assets. Working at the interface of biology and data, you’ll play a key role in unlocking insights from complex patient-level omics datasets...
As a Supplier Quality Engineer, you will lead the supplier quality management programme, working closely with Engineering, Manufacturing, and Quality teams to ensure suppliers meet regulatory, technical, and quality requirements. You will conduct supplier audits, manage quality agreements, and support design reviews and risk management, all while ensuring compliance with ISO 13485 and FDA 21 CFR Part 820.
This Quality Engineer role involves maintaining and improving the Quality Management System, leading audits and validations, and driving continuous improvement initiatives. You'll work across production, suppliers, and operational teams, ensuring compliance with AS9100, ISO 13485, and ISO 9001 standards.
This role involves designing and integrating optical systems into complex medical technologies, from early feasibility to product launch. You'll collaborate with a multidisciplinary team to develop devices that improve diagnostics, treatment, and patient outcomes, with a focus on precision, creativity, and regulatory compliance.
Label Strategy Manager (Devices) - EuropeLocation: Maidenhead/Remote (Hybrid working model)Contract: Temporary, full-time (7‑month maternity cover), starting July 2026Rate: Negotiable - circa. £60-70 per hourAn exciting opportunity has arisen for an experienced Label Strategy Manager (Devices) to join a European labelling...
As a Commercial Partnerships Manager, you will drive impactful collaborations and partnerships to accelerate the transition to human-specific research methods. You will secure sponsorships, grow supplier relationships, and manage the antibodies database to ensure it is a core commercial platform. Your role involves representing the Centre for Human Specific Research, building relationships with stakeholders, and aligning scientific innovation with real-world impact.
Are you an experienced Quality Coordinator with a background working within a regulated manufacturing environment such as Cosmetics, Medical Devices, Pharmaceuticals or similar? If so, this role could be for you!We are partnered with an extraordinary Cosmetics Contract Manufacturer who...
Mechanical Engineer | Bristol (Hybrid)We're working with a global engineering leader in the semiconductor manufacturing equipment sector to find a Mechanical Engineer to support the delivery of complex, high-tech systems used across advanced global manufacturing processes.This is a strong opportunity...
As a Senior Biomedical Engineer, you will be responsible for performing preventative maintenance, completing repairs, and managing administrative tasks related to medical equipment at the Princess Royal Hospital. You will also assist junior engineers and maintain spare part stock, ensuring all tasks are completed according to manufacturers' guidelines.
Senior Structural EngineerWarwick / up to 3 days remoteAbout the RoleYou’ll be working as part of an enthusiastic and committed team of Engineers and Technicians to deliver high quality output on projects. Client care and repeat business is crucial to...
This role involves designing and implementing quality test procedures for both software and hardware in medical device products. Responsibilities include attending design meetings, writing test plans, and ensuring compliance with regulatory standards.
This role involves designing and implementing quality test procedures for both software and hardware components of medical devices. Responsibilities include attending design meetings, writing test plans, analyzing opportunities for automated testing, and ensuring compliance with regulatory standards.
Bank Specialist Physiotherapist| Women's Health | Competitive Hourly Rate | Flexible Working | Fylde CoastWe have an exciting opportunity for an experienced Specialist Physiotherapist in Women's Health to join our bank staffing to support the Physio department on a flexible...
This role involves performing preventative maintenance and repairs on medical equipment in UK hospitals, supporting the site manager and team leader in achieving contractual KPIs, and maintaining safe working practices. The job requires strong customer relationship skills, familiarity with regulatory standards, and experience in a clinical environment.
This role involves leading a team in the design and optimisation of chemical processes for drug development. Responsibilities include technical direction, project delivery, regulatory submissions, and mentoring scientists. The position leverages innovative technologies and AI to enhance process efficiency and ensure robust commercial processes.
