Senior Regulatory Affairs Specialist

Excellence in Witney for the development and manufacture of electrodes and biosensors used by patients and healthcare professionals for the day-to-day management of diabetes.The site has been instrumental in the research, development and manufacture of the FreeStyle Libre Flash Glucose Monitoring System as well as exciting developments in the Libre family including FreeStyle Libre 2, FreeStyle Libre 3 and the Libre Sense system. We are passionate about doing work that improves the quality of people's lives.We're hiring a Senior Specialist Regulatory Affairs to join the EMEAP regulatory affairs team, which is growing to meet the demands of the business and to support a strong product pipeline.Primary Job FunctionYou will be responsible for a portfolio of cutting-edge medical devices & IVDs, leading regulatory activities for new product introductions and significant on-market changes for the Europe, Middle East, Africa and Pakistan (EMEAP) region. You will work as part of a global team,
to develop, lead and implement strategies that will ensure the timely introduction of new products onto the international market in a fast-paced environment.You will coordinate and oversee preparation of complete and scientifically sound regulatory submissions and lead interactions with the Notified Body and country regulatory contacts to facilitate the regulatory submission review process to ensure a timely approval process. Core Job ResponsibilitiesFormulate, develop and lead business critical regulatory strategies for the EMEAP region.Act as the regulatory subject matter expert in design control projects, assessing changes and managing roll out programs for existing products and new launches.Become a technical expert in ADC devices and support interactions with EU Notified Body/UK Approved Body, as well as competent authorities, as requiredManage the creation and development of EU & UK Technical files in accordance with MDR 2017/745, IVDR 2017/746 and other application

regulations.Provide coaching and mentoring to more junior team membersIdentify and implement process improvements and efficiencies per the global regulatory affairs strategy.EducationBachelor's degree or equivalent preferably in a Scientific discipline e.g. Chemistry, life Sciences, Biology.Minimum Experience RequiredKnowledge of MDR 2017/745 Regulations and ISO13485 is essential, additionally, knowledge of IVDR 2017/746 is preferredExperience within a medical device or healthcare manufacturing industry in a regulatory or quality role.Experience of Technical File creation and maintenance, as well as post market changesExperience of working with Notified Bodies and/ or other regulatory bodiesYou need to have excellent written and oral communication skills necessary to be able to produce succinct reports and documentation and to effectively communicate with other departments, managers and external regulatory organizations.In addition to a competitive salary,
Abbott offers a highly attractive benefits package which includes a defined-contribution pension scheme, a share ownership scheme, private healthcare, life assurance, and a flexible benefits scheme which you can tailor to your own requirements.The base pay for this position is N/AIn specific locations, the pay range may vary from the range posted.JOB FAMILY:Regulatory OperationsDIVISION:ADC Diabetes CareLOCATION:United Kingdom > Witney : Production FacilityADDITIONAL LOCATIONS:WORK SHIFT:StandardTRAVEL:Yes, 5 % of the TimeMEDICAL SURVEILLANCE:Not ApplicableSIGNIFICANT WORK ACTIVITIES:Not Applicable