Job Title Development Technician I Location(s) Oxford, UK - Oxford Immunotec About Us Revvity is a developer and provider of end-to-end solutions designed to help scientists, researchers, and clinicians solve the world’s greatest health challenges. We pair the enthusiasm of an industry disruptor with the experience of a longtime leader. Our team of 11,000 colleagues from around the globe are vital to our success and the reason we’re able to push boundaries in pursuit of better human health. Find your future at Revvity This position is a member of the Development Team and is specifically responsible for design, performance, and interpretation of experiments in support of Oxford Immunotec / Revvity's product development. This position will support both development of automated solutions and broader development objectives. Overall Responsibilities: Working closely with the automation and development scientists and engineers, senior development scientists, responsible for experiments that are designed and conducted in line with overall product development strategy within the company. Specific deliverables for the role are: With direction from their supervisor, taking responsibility for the design and conduct of experiments supporting lab automation and product development goals. When required operate as a scientist in support of running of the ODL, ensuring that the Quality Management System, including, ISO 13485:2016, and ISO 17025:2005, is adhered to at all times and in all aspects of the job Ensuring that work is completed to agreed timelines. Ensuring that any likely delays or issues with a given project are communicated to their supervisor in a timely manner. With significant input from their supervisor, prioritising workload to ensure key objectives agreed with supervisor are met on time. Support organisation, execution, and analysis of clinical trials, in collaboration with Clinical Affairs team, when required (preparation of paperwork/shipping of reagents/lab training/data collation). Represent OI at clinical sites outside of UK for extended periods of time (minimum of 1 month). Performing duties in other departments, on an occasional basis to meet critical Company objectives as required. Ensuring that projects are carried out in accordance with the Company Quality System and to the required Regulatory standards. Ensuring that conclusions in written reports reflect the data presented and reports are of the highest quality. Role Requirements: Desirable Technical skills and abilities: An understanding of the diagnostic and pharmaceutical industries Familiarity with Quality System concepts and requirements including GMP and ISO systems. Previous experience in protocol/report writing/handling of data with minimal supervision. Essential Technical skills and abilities: Knowledge of Windows and Office bases applications; Word, Excel, PowerPoint. Degree or Equivalent Ability to organise and prioritise work loads Previous work experience What we offer: Purposeful work environment Dynamic culture in which customers are at the forefront Being part of a highly qualified team that is committed to excellence Access to cutting-edge expertise through which you can make positive impact in the world around us Benefits package including private healthcare, life insurance, company pension and more