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apply with randstad.
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we'll give you a call.
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getting you registered.
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compliance check.
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reference and background check.
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the perfect job for you.
Our expert team will either arrange an interview for the role you’ve applied for, or if they believe there’s a better opportunity, they’ll suggest alternative options too.
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the interview.
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start your new job.
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¥16,000,000 - ¥19,000,000 per year, 年収1,600 ~ 1,900万円
社名社名非公開職種安全性管理、品質保証、品質管理業務内容Job Description:This position is the main Quality contact in Japan and will have strong experience in GxP’s, GQP and Quality Management Systems (QMS) and will have worked in an global Quality environment. This role will lead the implementation and execution of the local and Enterprise Quality System (SOP’s and Technology) and support compliance to current regulations, procedures and standards across the business.They will be a k
社名社名非公開職種安全性管理、品質保証、品質管理業務内容Job Description:This position is the main Quality contact in Japan and will have strong experience in GxP’s, GQP and Quality Management Systems (QMS) and will have worked in an global Quality environment. This role will lead the implementation and execution of the local and Enterprise Quality System (SOP’s and Technology) and support compliance to current regulations, procedures and standards across the business.They will be a k
¥10,000,000 - ¥15,000,000 per year, 年収1,000 ~ 1,500万円
社名社名非公開職種薬事、メディカルライティング業務内容オンコロジーに強み持つ日本立ち上げ段階の企業の募集です多くのパイプラインを有しており、今後が期待される企業です少数精鋭の組織のため経験者を歓迎しております求められる経験• BA/BS Degree in sceintific disciplines, MS/PhD preferred• 3+ years of related pharmaceutical or pharmaceutical industry regulatory CMC experience with proven record of experience in global submissions for clinical trial/market applications and subsequent response to HA queries.• Experiences to prepare CTD M2.3 and M1.2 (Application Form).• Exper
社名社名非公開職種薬事、メディカルライティング業務内容オンコロジーに強み持つ日本立ち上げ段階の企業の募集です多くのパイプラインを有しており、今後が期待される企業です少数精鋭の組織のため経験者を歓迎しております求められる経験• BA/BS Degree in sceintific disciplines, MS/PhD preferred• 3+ years of related pharmaceutical or pharmaceutical industry regulatory CMC experience with proven record of experience in global submissions for clinical trial/market applications and subsequent response to HA queries.• Experiences to prepare CTD M2.3 and M1.2 (Application Form).• Exper
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