This role involves leading the regulatory strategy for a cardiology medical device company, focusing on FDA, CE, and UKCA submissions, and ensuring compliance with international regulations. You will work closely with the senior team and regulatory bodies, driving the company's expansion into new markets.
This role involves leading the development and integration of microfluidic technologies, including droplet generation, flow control, and droplet sorting. The candidate will work across multidisciplinary projects, design and develop microfluidic devices, and integrate optical systems for high-throughput screening of enzymes.
This role involves designing and developing FPGA functionality using VHDL, and writing embedded software in C to control hardware and interface with FPGA-based systems. You will collaborate with hardware and software engineers to integrate and optimize new features in complex electronic products, supporting cutting-edge scientific research.
This role involves designing and developing internal applications and web-based tools to support scientific research and drug discovery. You will work closely with bioinformaticians, data scientists, and biologists, using technologies like .NET, C#, JavaScript, TypeScript, and React.
This role involves maintaining quality and regulatory compliance for a Class I medical device, overseeing supplier quality, reviewing batch documentation, and supporting audits and post-market surveillance. The position is part-time, working 2.5 days per week, and offers the opportunity to take ownership of compliance activities within an established healthcare packaging division.
This role involves hands-on, multidisciplinary engineering to design and develop complex medical devices, working closely with a diverse team of specialists. The projects span multiple medical specialisms, including surgical robotics, but the role requires a broad interest in various device types and engineering challenges.
This role involves managing product quality issues, leading root cause investigations, and working with Engineering, Production, and Supply Chain to drive continuous improvement. Key responsibilities include structured problem-solving, supporting new product introductions, and monitoring quality performance measures.
As a Van Driver at Movianto, you will deliver pharmaceutical products efficiently and safely, ensuring compliance with health and safety regulations. You will operate company vehicles, perform daily maintenance checks, and maintain a professional appearance while adhering to legal requirements and company policies.
This role involves designing and developing novel mechatronic systems for medical devices and biotechnology products, working within a multidisciplinary team to iterate and refine solutions until they are ready for manufacture. The focus is on intricate mechanisms and overall system development.
This role involves leading complex clinical technology transformation and data migration initiatives across the clinical trial ecosystem. Responsibilities include managing end-to-end migration programmes, data validation, and ensuring compliance with regulatory requirements. The position requires strong clinical technology expertise and project management skills.
This role involves leading the strategy, negotiation, and execution of global and local Pharmacovigilance Agreements, ensuring alignment with regulatory requirements and business objectives. The Director will manage a team responsible for alliance contracting, governance, compliance, and operational excellence, while fostering strong partnerships and driving continuous improvement and digital transformation.
This role involves delivering high-quality teaching and assessment in biomedical and mechanical engineering, developing engaging teaching materials, and supervising students. You will also contribute to curriculum design, research, and professional practice, and engage in student recruitment and support activities.
This role involves leading multiple programmes focused on advancing next-generation drug delivery platforms, mentoring junior engineers, and taking ownership of core mechanical design activities. The position requires a strong background in mechanical engineering, experience with drug delivery devices, and the ability to balance technical innovation with commercial viability.
Lead the development of medical devices from concept to commercial launch within a multidisciplinary engineering team. Drive project execution with a focus on high-volume manufacturability, particularly using injection-moulded plastics, while mentoring junior engineers and ensuring regulatory and design compliance. Play a key role in shaping technically robust, patient-focused medical technologies in a fast-paced environment.
This role involves providing hands-on regulatory support for a diverse portfolio of complex engineering projects, working closely with design engineers and project teams to ensure compliance with international standards. You will contribute to the quality management system, interpret regulatory requirements, and help navigate compliance considerations while supporting innovation.
