At EY, you’ll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture and technology to become the best version of you. And we’re counting on your
Date Posted: 2024-05-15 Country: Japan Location: Shiroyama Tower (PW Japan HQ/UTIO HQ): Shiroyama Trust Tower 30F 4-3-1 Toranomon, Minato-Ku, Tokyo, 105-6030 JAPAN Position Role Type: Unspecified Pratt & Whitney is working to once again transform the
The Role This position will provide administrative support to the Group. Job Responsibilities Administrative role at Asset Management Division Support of Asset Management Division regarding payment request to trust banks and accounting firms. Preparation of payment
Job Requisition ID # 24WD78669 Position Overview Autodesk is seeking an experienced contract professional who will be responsible for drafting, negotiation, interpretation, and/or administration of contractual documents with some of Autodesks most significant APAC customers. This
職種 正社員 職務明細 Christian Dior G.K. is looking for Store Planning Manager due to business expansion. This position will report to Store Planning Director. This positions key missions are as follows: Responsible of the entire process of
Are you an experienced Procurement Manager with a passion for renewable energy? We are continuing our international expansion and searching for experienced supply chain and procurement professionals to work on projects in Japan, the wider APAC
Job Description Purpose Enhance customer satisfaction levels while attaining DOS(Days of Supply: clitical metrics to measure how long the inventory on hand), Net inventory, and cash flow targets. • Supply to business growth as shared services
Description Key responsibilities 1. Directly manage a medium sized team responsible for effective execution of Dr. Ci:Labo programs in alignment with category strategies driven efficiently through the most efficient technologies using aligned work processes. 2. Stakeholder
As a clinical trial manager, you oversee the planning, execution, and monitoring of clinical trials, ensuring adherence to protocols, timelines, and regulatory requirements while collaborating closely with cross-functional teams to drive successful trial completion and contribute
Take lead in medical writing activities in authoring clinical/regulatory documents as well as submission requirements to obtain product approval. Align with global business strategies for local requirements Client Details * One of the top global biopharmaceutical companies
Our client is a global leader in health technology, focused on improving peoples lives through meaningful innovation. With a diverse portfolio spanning healthcare, lighting, and consumer lifestyle products, our client is dedicated to delivering cutting-edge solutions
