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 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.
The Regulatory Affairs Manager will lead day-to-day regulatory activities, maintaining and developing technical documentation for existing and future medical devices and IVD products. You will support UKCA and CE marking, contribute to regulatory strategies, and collaborate with scientific, data, and technical teams to ensure compliance throughout product development.
This role involves supporting market access, quality systems, and governance in a healthcare and technology environment. Responsibilities include managing regulatory and technical documentation, ensuring CQC compliance, and coordinating evidence for audits and inspections.
The Senior Regulatory Affairs Specialist leads and supports regulatory activities for medical devices, including strategy development, impact assessments, and submission preparation for the US and international markets. The role involves collaborating with project teams, regulatory authorities, and internal stakeholders to ensure compliance and efficiency in regulatory processes.
This role involves leading regulatory strategy and compliance for medicinal products, medical devices, and cosmetics in the UK and Ireland. Responsibilities include managing regulatory submissions, supporting product launches, and maintaining relationships with regulatory authorities like MHRA and HPRA.
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 leading the Medical Affairs team to develop and implement medical strategies, evidence generation, and governance frameworks. Responsibilities include collaborating with cross-functional teams to ensure scientific rigor and compliance in supporting the product lifecycle.
The Clinical Research Scientist will work on the clinical development strategy for large studies and programs in cardiovascular and metabolic diseases, collaborate with global regulatory affairs, and represent the organization at medical congresses. The role involves overseeing communication strategies, driving innovation, and mentoring team members.
Provides medical oversight for clinical trials to ensure patient safety, protocol compliance, and data integrity. Acts as primary medical contact for study teams and sites, reviewing adverse events, supporting safety monitoring, and guiding eligibility and dosing decisions. Collaborates with cross-functional teams to resolve issues and support regulatory submissions.
The Lead Content Compliance Specialist role involves coordinating and optimizing advertising and promotional material approval processes across EMEA. Key responsibilities include managing complex submissions, driving process improvements, and ensuring compliance with regulatory standards.
This role involves working on the development of next-generation imaging technology, including image segmentation hardware, signal processing, transducer design, and optical systems. You will build prototypes, conduct experiments, and work closely with a team of experienced inventors to push technological boundaries.
This role involves shaping growth strategies, modernizing platforms, and delivering differentiated digital and AI capabilities for the Surgery portfolio. The leader will partner with senior business leaders to develop technology as a competitive advantage and drive innovation across the region.
The Compliance Engineer will be responsible for creating, reviewing, and maintaining regulatory and technical documentation to ensure products remain compliant and audit-ready. Key responsibilities include authoring technical files, supporting EU MDR and UK regulatory compliance, and assisting with Notified Body and external audit requirements.
This role involves providing technical leadership and shaping the software architecture for a wearable medical device platform. The engineer will work across software, signal processing, and firmware teams to ensure compliance with medical standards like IEC 62304 and support regulatory approval. The position is hands-on, requiring active development, code reviews, and troubleshooting while guiding internal and external engineering efforts.
