Future Tech Jobs
Future Tech Jobs
Regulatory Affairs Specialist - MedTechA growing medical devices company in Cambridgeshire are currently in need of an experienced quality assurance and regulatory affairs specialist.This is an excellent opportunity for a QARA specialist to join this team of experts and work...
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.
The Regulatory Affairs Specialist will ensure compliance with UK MDR and EU MDR requirements, maintain technical documentation, and support regulatory submissions for Class I and Class IIa medical devices. You will work closely with the QA Manager to improve the Quality Management System and coordinate post-market surveillance activities.
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.
Regulatory Affairs Manager EU, clinical trials, post approvalYour new companyAn exciting opportunity has arisen for an experienced Regulatory Affairs Manager to join a leading global biotechnology organisation. Working within the European Regulatory Affairs team, you will play a critical role...
Our client:* A global leader in ingredient solutions, supporting innovation across food, beverage, and nutrition markets.* Driving growth through strategic partnerships with retailers, manufacturers, and health-focused brands.* Renowned for high-quality, functional ingredients that help brands meet evolving consumer needs.The role:*...
This role involves managing regulatory compliance for advanced wound care medical devices throughout their lifecycle. The specialist will lead global regulatory submissions, support new product development, and ensure adherence to standards like ISO 13485 and FDA regulations. Collaboration with cross-functional teams and engagement with regulatory authorities are key to securing approvals and maintaining product registrations worldwide.
This role involves leading regulatory strategy and compliance for medicinal products, medical devices, and cosmetics in the UK and Ireland. The specialist will manage submissions, support product launches, ensure compliance with MHRA and HPRA, and maintain regulatory documentation. It requires strong post-Brexit regulatory knowledge and collaboration with global teams.
Leads the European Regulatory Affairs team at GE HealthCare, defining regulatory strategy and ensuring compliance with EU MDR and UK MDR for medical devices. Oversees CE and UKCA marking, manages interactions with Notified Bodies and Competent Authorities, and drives regulatory alignment across quality, legal, and product teams. Focuses on strategic planning, postmarket compliance, and industry engagement in a global healthcare technology environment.
This role involves supporting regulatory and quality processes within a healthcare organisation, focusing on documentation control, customer feedback management, and compliance with medical device regulations. The administrator will coordinate cross-functional communication, maintain quality systems, and ensure accurate record-keeping across product safety and regulatory submissions. It offers exposure to pharmacovigilance, regulatory standards, and product lifecycle management in a collaborative team environment.
This role involves supporting the Quality Management System (QMS) and Regulatory processes, including ISO13485 readiness and FDA 510(k) documentation. You will work closely with internal teams to maintain quality documentation, manage change controls, and promote continuous improvement.
Your new companyAre you an experienced Senior Medical Writer looking for your next long-term contract opportunity?I am currently partnering with a leading global pharmaceutical organisation seeking a Senior Medical Writer to join their clinical and regulatory writing team on an...
This role involves leading the global product strategy for a patient hygiene portfolio within a healthcare manufacturing organisation. The Product Manager will identify market opportunities, guide product development from concept to launch, and collaborate with cross-functional teams including marketing, R&D, and sales. The position focuses on delivering innovative healthcare solutions that improve patient outcomes internationally.
This role involves providing quality assurance leadership for the development and clinical manufacturing of diagnostic radiopharmaceuticals. The QA Manager will oversee GMP compliance, support technology transfer, manage CMO relationships, and ensure quality systems are integrated across R&D and clinical operations. Key responsibilities include leading investigations, supporting audits and inspections, and driving continuous improvement in quality processes.
This role involves providing scientific and clinical leadership across global clinical development programs, shaping clinical strategy, and ensuring high-quality execution of trials from design to regulatory submission. The director will lead cross-functional teams, oversee clinical data analysis, and contribute to safety monitoring and regulatory interactions. It offers the chance to work on innovative therapies within a collaborative, matrixed environment.
