リファイン すべてリセット
距離:
ソート
雇用主/採用担当者
掲載日
職種
雇用主/採用担当者
経験
すべてのフィルタ

Regulatory Submissionsの求人-taitō - 60 Job Positions Available

60 / 1 - 20 求人
Amgen 求人

Career CategoryRegulatory Job Description Group Purpose The Compliance Group is responsible for MAH business license, Three-supervisors’ committee (Sanyaku-kaigi), Foreign Manufacturer Accreditation/ Foreign Manufacturer Registration (FMA/FMR), periodic GMP inspection, and other activities to ensure compliance the Act

Amgen  16日前
Johnson & Johnson 求人

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our

Johnson & Johnson  15日前
HSBC 求人

HSBC Asset Management (“AM”) Product Group is responsible for the strategic and commercial development of AM Product manufacturing capabilities including Development, Management, Governance, Support and Mandate delivery across all Global Markets. The product function is expected

HSBC  9日前
HSBC Group 求人

HSBC Asset Management (“AM”) Product Group is responsible for the strategic and commercial development of AM Product manufacturing capabilities including Development, Management, Governance, Support and Mandate delivery across all Global Markets. The product function is expected

HSBC Group  9日前
CooperCompanies 求人

CooperVision Japan (CVJ) is the largest operating business in the APAC region, based in Tokyo and is the second largest single country businesses in worldwide. Japan RA Senior Specialist (hereinafter referred as the RA Senior Specialist)

CooperCompanies  8日前
Lundbeck 求人

Overall Purpose of the role Regulatory Affairs in Japan is responsible for the local regulatory affairs function, ensuring compliance with Japanese regulatory requirements, and aligning strategies with global objectives. This role leads regulatory strategy in Japan for specific portfolio projects,

Lundbeck  8日前
Abbvie 求人

企業概要 About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples

Abbvie  6日前
Western Union 求人

Analyst, Regulatory Compliance Operations, Tokyo, Japan Role Responsibilities This position is responsible for supporting Western Union Japan KKs (WUJKK) regulatory compliance framework and ensuring adherence to applicable regulatory requirements, licensing obligations, and reporting requirements established by the Japan Financial

Western Union  6日前
Abbvie 求人

企業概要 About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples

Abbvie  1日前
Ramboll 求人

Job Description Senior Consultant Health Science (Product Stewardship/Regulatory Affairs) Plant Protection Team, Tokyo, Japan Inviting bright minds Do you want to push the boundaries of your profession and develop your excellence in an open, collaborative and empowering

Ramboll  17時間前
CooperCompanies 求人

CooperVision Japan (CVJ) is the largest operating business in the APAC region, based in Tokyo and is the second largest single country businesses in worldwide. Japan RA Specialist (hereinafter referred as the RA Specialist) shall be

CooperCompanies  1日前
Sanofi 求人

Job title: Manager, Regulatory Affairs Location: Tokyo About the job Role & Responsibilities The R&D Regulatory Affairs has responsibility for managing products under development and/or marketed products with new indications. Develop regulatory strategy for new drug developments, Health Authority

Sanofi  5時間前
Sanofi 求人

Title: Senior Quality Specialist Location: Japan HQ - About the job As Senior Quality Specialist (Expert Japan) within our Vaccine R&D Quality Operations team, youll lead all quality-related activities for Vaccine R&D in Japan, ensuring compliance

Sanofi  29日前
ICON plc 求人

Manager, FSA - Tokyo Osaka - Office Hybrid/Home ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity,

ICON Plc  29日前
IBM 求人

Introduction A career in IBM Consulting is built on long-term client relationships and close collaboration worldwide. You’ll work with leading companies across industries, helping them shape their hybrid cloud and AI journeys. With support from our

IBM  24日前
Boehringer Ingelheim 求人

Basic Purpose of the Job Key contact partner in cultivating the power of data through: Data collection/curation, data review and data delivery Data standardization Process definition, testing and training Responsibilities include: Translating scientific requirements into technical

Boehringer Ingelheim  24日前
Pfizer 求人

Job Description 1. Objectives Responsible for clinical development of the assigned project in Japan under the supervision of the Japan Development Leader (JDL), who assumes responsibility for development of all projects in Japan in the respective

Pfizer  22日前
GSK 求人

Job Purpose The Clinical Development Lead (CDL) in Japan is the single point of accountability for all clinical development activities for assigned asset(s). The CDL provides scientific and medical leadership to define and deliver Japan clinical

GSK  22日前
Abbvie 求人

企業概要 About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples

Abbvie  21日前
PSI CRO 求人

Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring

PSI CRO  20日前

新しい機会を逃さないで!

確認メールの送信先

メールを確認し、リンクをクリックして求人情報の受信を開始します。

最新の求人情報を受け取ることができます。

regulatory submissions 求人 全国 taitō

次も興味があるかもしれません:

Japanese

Regulatory Requirements

Clinical Development

Regulatory Affairs

Clinical Trials

Pharmaceutical Industry

Efficacy

Clinical Research

Oncology

Governance

確認メールの送信先

メールを確認し、リンクをクリックして求人情報の受信を開始します。

すべてのフィルタ 申請する
ソート
雇用主/採用担当者