Regulatory Affairs Associate - Global Medical Devices company - North Yorkshire with hybrid working - £competitive basic salary, bonus, pension, healthcare, 25 days holiday + BHThe CompanyA market leading, global medical devices company focusing on multiple therapy areas. Their highlights include;Global medical devices companyDistribute a range of devices from Class I-III across multiple therapy areasAward winning companyExcellent training and development opportunitiesIdyllic location with plenty of onsite parkingThe RoleCompleting regulatory dossiers for global submissions, including 510(k) applicationsMaintain existing products, managing variations and renewalsEnsure all products remain compliantAssist with both internal and external audits from a regulatory perspectiveYou2 years+ experience in Regulatory Affairs specifically within medical devicesGood knowledge of MDRKnowledge of ISO 13485Ideally experience with 510(k) applicationsDue to their location, you will need to have a driving licence and access to a vehicle on office daysWhat should you do next?This Regulatory Affairs Associate role is one not to be missed; it encompasses the opportunity to work with a global medical devices company. To discuss this role further or to find out about other roles I'm currently working on, please get in touch or hit apply to submit your current CV.Unless otherwise stated, if applying for a job within the UK or European Union, you must ensure that you are to work there.Carrot Recruitment acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, colour, sex, age, national origin, religion, sexual orientation, gender identity and/or expression.If there are any arrangements or adjustments we can make to assist you at interview then please let us know and we'll be more than happy to assist.
