薬事

ロバート・ウォルターズは1985年に英国ロンドンで設立されたスペシャリスト人材紹介会社です。世界中の主要都市にオフィスを構え、日本においては2000年に東京オフィス、2007年に大阪オフィスを設立。主に外資系/日系グローバル企業におけるバイリンガル・スペシャリストの転職において優れた信頼と実績を築いてきました。日本では正社員、派遣/契約社員のキャリアアップをサポートしております。

検索結果

Product Regulatory Specialist/プロダクトレギュラトリペシャリスト

給与: ¥8000000 - ¥10000000 per annum

勤務地: Kanagawa

掲載日: 2016/11/24

A global chemical company is currently recruiting a Product Regulatory Specialist, a dynamic role suitable for a certified pharmacist with strong project management skills. This position will see you supporting pharma and nutrition product work including FMA and API registration and GMP certificate application and maintenance.
Regulatory Affairs Specialist/レギュラトリアフェアーズスペシャリスト

給与: ¥8000000 - ¥15000000 per annum

勤務地: Tokyo

掲載日: 2016/11/14

A global pharmaceutical company is in search of an individual with a degree in pharmacy, biology, or chemistry plus several years’ experience in R&D to join its team as Regulatory Affairs Specialist. This is a highly multifaceted role suitable for an experienced professional who will evaluate candidate products, interface with regulatory authorities, and work closely with global RA.
Senior RA Specialist/シニアRAスペシャリスト

給与: ¥6000000 - ¥8000000 per annum

勤務地: Tokyo

掲載日: 2016/11/11

A global pharmaceutical company is recruiting for the position of Senior RA Specialist. The candidate selected for this role will be educated to bachelor degree level and possess at least 5 years’ experience in R&D or regulatory affairs at a pharmaceutical company. This dynamic role will see you working closely with global RA and interfacing with regulatory authorities.
Regulatory Affairs Manager/薬事マネージャー

給与: ¥8000000 - ¥12000000 per annum

勤務地: Tokyo

掲載日: 2016/11/10

A global pharmaceutical company is recruiting for the senior role of Regulatory Affairs Manager. Primary responsibilities include providing regulatory development and registration strategy, facilitating negotiations, and contributing to global regulatory activities. An individual with a science degree/background and new drug approval experience would be an ideal match for this position.
Regulatory Submissions Manager/レギュラトリサブミションズマネージャー

給与: ¥8000000 - ¥12000000 per annum

勤務地: Tokyo

掲載日: 2016/11/10

A leading drug development services company is searching for an individual with experience in the pharmaceutical industry and deep regulatory knowledge to join them as the Regulatory Submissions Manager. This is an exciting opportunity to use your talents as a member of a global institution.
Clinical Documentation/クリニカルドキュメンテーション

給与: ¥5000000 - ¥7000000 per annum

勤務地: Tokyo

掲載日: 2016/11/10

外資系医薬品メーカーにて医薬品の承認申請業務を担当いただきます。理系の博士号をお持ちの方で、承認申請関連業務に携わったご経験をお持ちの方、是非この機会に奮ってご応募ください。このポジションのお問合せやご相談がありましたら、担当コンサルタントまでお気軽にメールまたはお電話にてご連絡ください。
RA Specialist/RAスペシャリスト

給与: ¥6000000 - ¥9000000 per annum

勤務地: Tokyo

掲載日: 2016/10/17

ヘルスケア商品で世界的に有名な企業にて、医療機器の薬事申請業務を担当いただきます。3年以上の同様の経験必須となりますが、薬事以外でも臨床、品質保証、安全管理などをご経験された方は考慮させていただきます。世界的な大企業にて経験を伸ばすチャンスです。ふるってご応募ください。