Medical Device Engineer (Polymer Science)

Currently I am assisting a medical device company recruit a Medical Device Engineer to join an exciting team in growth mode. The company is seeking a highly skilled Medical Device Engineer with a strong background in polymer chemistry. As a vital member of our team, you will play an essential role in the development, production and testing of our innovative medical device. Key Responsibilities * Conduct R&D activities to improve the polymer-based device formulation to meet the desired properties and medical device specification. * Utilise in-depth knowledge of polymer science to design, optimise and develop production processes, ensuring efficiency and quality in the manufacturing of polymer-based materials. * Support efforts in scaling up polymer-based processes from laboratory to pilot-scale production, ensuring seamless transition and efficiency. * Design, optimize, and validate new testing protocols. * Maintenance and qualification of laboratory equipment * Maintain comprehensive records, including experimental data, observations, and outcomes, following strict documentation protocols and QA/RA Requirements * Contribute actively to the implementation and improvement of H&S requirements. * Produce weekly reports on progress. * Create and manage the design history files and technical files for the product. * Support product regulatory submissions. Qualifications * A master’s degree in Organic Chemistry or Chemical Engineering with a background in Polymer Science * At least 4-5 years proven industrial experience in a production or manufacturing and characterisation, in roles directly related to polymer science. * Demonstrated expertise in polymer characterisation, processing, and synthesis techniques. * Experience in working with hydrogels. * Previous experience within an R&D Laboratory or materials development environment * Experience in experimental design and proficient data analysis skills. * Excellent written and oral communication skills * The ability to handle priorities effectively to meet deadlines under pressure through effective time management. * Self-motivated and capable of working with minimum supervision. * Be able to meet the challenges of a fast-paced start-up and provide innovative ideas to the technical team. Desirable * Working knowledge of Medical Device Quality Management System (ISO 13485). * Experience in creating documentation for regulatory compliance (for example: FDA, CE, etc) * Experience with design reviews and design controls