\Appeal points/ · ◆A global company with over 220 years of history · ◆A company with a US headquarters · ◆A company with a fusion of both foreign and Japanese companies, so you can use your English · ◆A hybrid work system makes it easy to maintain a work-life balance · ◆Productio ...

JOB PURPOSE · The Manger, Regulatory Affairs, Japan shall manage regulatory activities assigned in GW Pharma order to obtain new drug application(NDA) approval, partial change application(PCA) approval, to submit appropriate minor change notification(MCN) and to execute other ne ...

Are you experienced in CMC regulatory affairs or in generating high-quality documentation related to drug manufacturing and marketing approval/maintenance? Do you have a strong understanding of CMC requirements in Japan? We are seeking a CMC Expert to join our team and contribute ...

The position · The CMC Expert is in charge of obtaining approval and maintaining marketing authorization by generating high-quality documentation aligned with Regulatory/CMC requirements in Japan and NN standards. Additionally, the CMC Expert is tasked in developing CMC associat ...

En DuPont, trabajamos en cosas que importan, ya sea en proporcionar agua limpia a más de mil millones de personas en el planeta, producir materiales esenciales en los dispositivos tecnológicos cotidianos (desde smartphones hasta vehículos eléctricos) o proteger a los trabajadores ...

Are you an experienced medical professional and passionate about Medical Affairs? Are you a dynamic leader with a passion for driving MSL team? If so, we have an exciting opportunity for you to join our team as a Medical Scientific Liaison (MSL) Manager at Novo Nordisk. Apply tod ...

The position · Ensure personal and professional development of the MSL team; and ensure coordination and cooperation between the MSL team, the MSL Supervising Group Manager (SVM), and other relevant stakeholders. Represents the MSL team internally within the affiliate and in ext ...

Description · The role is responsible for developing and executing medical strategies/tactics to maximize patients' access to our innovative therapies. The role holds a critical responsibility to provide the team with latest scientific & technical knowledge for in-line and pipel ...

The position · As a HEOR Specialist, you will have the opportunity to implement Health Economic Outcomes Research (HEOR) projects in line with value proposition, market access, and scientific exchange strategies for assigned products and therapeutic areas. You will also support ...

The position · The CMM will facilitate execution of clinical trials related to New Therapy Areas including CKD (Chronic Kidney Disease), CVD (Cardiovascular Disease), Liver Disease, inflammation and Alzheimer's disease (AD), by providing medical/scientific expertise and advice b ...

The position · This Senior Manager/Director for Brand Marketing will create strong, impactful, measurable, and globally aligned marketing strategies and execution tactics to deliver the Insulin business and total Diabetes business, ensuring both short and long-term success in th ...

Are you interested in improving the lives of millions of people, contributing to a company that works with innovation and is a pioneer in addressing the unmet medical needs? Do you have an innovative mindset to drive change in a future-ready environment? If yes, this position of ...

Are you passionate about implementing Health Economic Outcomes Research (HEOR) projects? Do you want to make a meaningful impact on patient lives? We are looking for a HEOR Specialist to join our Market Access team at Novo Nordisk. If you are ready for a life-changing career, rea ...

The position · As a Non-Clinical expert, you will ensure the high-quality preparation of J-CTD (M.2.4. and 2.6) in collaboration with HQ. While most modules are Japanese translations of HQ's CTD, you must thoroughly understand each module's content and verify its accuracy. Modul ...

The position · As our Legal, Ethics & Compliance Counsel, you are expected to utilize expertise on legal and ethics & compliance, enable business in Japan to achieve growth initiatives while defending the company from major legal, compliance, and reputational risks.The role resp ...

Description · Lead preparation and submission of registration dossiers and obtain regulatory approval for the import of genetically modified crop seeds. · Partner with global regulatory team to align the regulatory direction with Corteva strategy. · Follow Japanese regulatory tr ...

Working with Us · Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production li ...

Do you have a strong background in non-clinical activities? We are looking for a Non-Clinical Expert to join our team at Novo Nordisk. If you are ready to contribute to the development, submission, and approval of new drugs/devices, and have a passion for maintaining existing pro ...

Are you ready to make a difference in the healthcare industry? Do you have a passion for marketing and driving business success? We are looking for a Senior Manager/Director for Brand Marketing to join our Insulin Marketing Group at Novo Nordisk. If you are a strategic thinker wi ...

Working with Us · Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production li ...