At Roche we focus on developing medicines and diagnostics that will help patients live longer, better lives.We strive to address unmet medical needs through excellence in science – from early detection and prevention of diseases to diagnosis, treatment and treatment monitoring. Job facts In your role as Regulatory Affairs Executive, you will report to Regulatory Affairs Manager and your main responsibilities will be: Prepare the registration dossier to comply with local regulation Check and request additional document to Head Quarter Submit the registration dossier and follow up with officers, experts to get the results in timely manner for assigned products Coordinate with medical team to update PI for assigned products Coordinate with person in charge of local content to get approval of drug label for assigned products and do checking labelling compliance Coordinate with Supply Chain Manager to declare the registration price for assigned products Prepare and apply the application and necessary formalities to get the registration samples for assigned products Who you are Who you are You’re someone who wants to influence your own development. You’re looking for a company where you have the opportunity to pursue your interests across functions and geographies. Where a job title is not considered the final definition of who you are, but the starting point. You have Pharmaceutical/Medical Degree. Further knowledge, skills and competencies are: At least 2 years working in pharmaceutical company Understanding of the pharmaceutical industry Communication skills Teamwork, good adaption Performance achievement Fluent English & Vietnamese communication Location Vietnam, Ha Noi Function Regulatory Affairs Subfunction Drug Regulatory Affairs Schedule Full-time Job level Individual Contributor Job type Regular Employee Division Roche Pharmaceuticals Posted since 2017/11/16 Job-ID 3428464510 Nguồn:www.roche.com