Job DescriptionAgilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek -- so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com.Are you an individual with knowledge in IVD or Medical Devices, looking for a new challenge in your career? A job where your actions will have an impact on improving quality of life. Then we are looking for you!Come and join a highly collaborative environment where you will be part of our Global Regulatory Affairs team with the opportunity to be exposed to innovative IVD products across different regulatory classifications including hardware, software, and immunochemistry technologies.We are searching for an experienced Regulatory Affairs Specialist to play a key role in coordinating and tracking international submissions mainly in the EMEA (non-EU) for new products along with renewals and changes to existing registrations.Your main task will be: Create, manage, and ensure closure of daily Regulatory blocksBecome an expert with the GTS tool handling Regulatory release of IVD productsCreate, train, and implement tools for accurate tracking of product changesCollaborate with Global Regulatory Affairs ensuring regulatory assessments of changes is sought, obtained, and documentedOversight of Channel Partner business licenses and renewalsOversight of IVD registrations and renewalsCollaborate with Global Regulatory Affairs ensuring timely registration of IVD products and their renewalsQualificationsA university degree in a relevant field such as Life-Science/Engineer/Law etc.Significant regulatory experience with a solid understanding of IVD/medical device regulations and registration requirements.Ability to interpret regulations and standards in relation to specific products.Excellent interpersonal and communication skills in EnglishIn order to succeed the successful candidate will have proven capability in analytical and critical thinking, collaborating across global teams, strong organization skills, ability to run multiple ongoing responsibilities, and driving tasks through to completion.We offer:An independent job in collaboration with good colleagues, in a growth-orientated organizationA true commitment to work/life balanceAn opportunity to learn and grow in the field of Regulatory AffairsAgilent Result Bonus, Stock Purchase Plan, Life Insurance, Pension, Healthcare, Employee Assistance Program, Holiday, Company activities.Pay range:45.296,00 - 70.775,00 EUR per annumThe position is classified at Levels 2 or 1 under the CCNL Terziario, distribuzione e servizi – Cod. H011, which defines minimum salary levels, pay progression, and working conditionsAdditional DetailsThis job has a full time weekly schedule. It includes the option to work remotely.Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locationsAgilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.Travel Required: OccasionalShift: DayDuration: No End DateJob Function: Quality/RegulatorySummaryLocation: Italy-Remote Location-MilanType: Tempo pieno

📌 Sr. International Regulatory Affairs Specialist - EMEA (Milano)
🏢 Agilent Technologies
📍 Milano