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過去24時間の求人情報

Regulatory Affairsの求人-東京 - 8 Job Positions Available

8 / 1 - 8 求人
Thermo Fisher Scientific 求人

Job Description Job Responsibilities: Develop and execute strategies that align with the global business units’ strategy. Focus business areas products include ImmunoDiagnostics and Molecular Diagnostics. and other areas may be added as appropriate. Identify and evaluate

Thermo Fisher Scientific  16時間前
Cargill 求人

Job Purpose and Impact The Industrial Chemical Regulatory Specialist II will ensure compliance with government chemical regulations or standards in the areas of product compliance, hazard communication, customer documentation and other regulatory functions. In this role, you will

Cargill  6時間前
Thermo Fisher Scientific 求人

Job Description When you’re part of the team at Thermo Fisher Scientific, you’ll do important work. Surrounded by collaborative colleagues, you’ll have the support and opportunities that only a global leader can give you. Our respected,

Thermo Fisher Scientific  16時間前
Thermo Fisher Scientific 求人

Job Description Job Summary: To ensure that clinical supplies are stored and distributed in accordance with Fisher Clinical Services (FCS) approved procedures and policies, cGMP, cGDP, and regulatory requirements. Maintain the FCS Japan Quality System in compliance

Thermo Fisher Scientific  16時間前
Mastercard 求人

Job purpose: Responsible for implementing the Medical Affairs Plan of specified Team strategies, driving a consistent approach to carrying out scientific engagement activities internally and in the field; ensuring compliance with all relevant regulations and GSK policy/code

Mastercard  7時間前
Mastercard 求人

Job purpose Medical Science Liaison (MSL) is a field-based role in the new Medical and Development organization, reporting to MSL Head. In order to build a trust with External Experts (EE) and scientific community through, MSL

Mastercard  7時間前
Michael Page 求人

* At the front line of communication with stakeholders at hospital sites / clinics, youll manage clinical aspects of full-service global trial projects. Your responsibilities will include ensuring timelines, targets, and standards are met for clinical

Michael Page  1時間前
Michael Page 求人

Take lead in diverse range of RA projects to support clients in obtaining regulatory approval. Provide expertise in RA strategy/development. Client Details * One of the largest global CROs in the industry * Partnering with small to

Michael Page  1時間前

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regulatory affairs 求人 全国 東京

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Japanese

Clinical Trials

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