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医薬品製造・品質管理に関する事務業務を担当します。 · 文章管理業務(作成、保管、管理) · 製品出荷に伴う記録書照査業務 · 製品品質照査業務 · ...

ブランクOK経験のある方は即戦力としてご活躍いただけます · 医薬品の品質試験 · ・機器を使用しての理化学試験 · ・試験に際しての前処理、後片付け · ・報告書の作成 · ...

ブランクOK経験のある方は即戦力としてご活躍いただけます · ・調達グループにおける事務業務 · ・伝票の入力作業、電話応対等 · ・庶務雑務8時30分~17時00分(実働7.75時間) · 休憩45分 · 残業月10時間程度 ...

ブランクOK経験のある方は即戦力としてご活躍いただけます工場検査部での一般事務・荷受業務(荷物の受取と伝票処理) · ・検査用図面の管理(検査用図面の整理と必要な図面を抽出し検査担当に回付) · ・検査成績書の作成及び必要な証明書の管理 · ・庶務雑務 · ...

ブランクOK経験のある方は即戦力としてご活躍いただけます · 設計部署での一般事務 · ・資料作成、データ入力 · ・庶務事務全般 · ・電話応対 · ...

We unite caring with discovery to make life better for people around the world. We are looking for people who are determined to make life better for people around the world. · ...

At Lilly, we unite caring with discovery to make life better for people around the world. · ...

We are looking for a Product Quality Assurance Associate to join our team at Lilly's Kobe Headquarter office. The successful candidate will be responsible for ensuring the quality of products and processes in accordance with regulatory requirements and company standards. · ...

We are looking for people who are determined to make life better for people around the world. · Risk-Learning Program (up to 2 years) · ...

p>At Lilly we unite caring with discovery to make life better for people around the world. We are looking for people who are determined to make life better for people around the world.Living allowance · Transportation fees etc. · ...

Quality assurance-related work will be performed. Data completeness confirmation for manufacturing instructions records and test records data storage status change middle product material achievement input warehouse manufacturing area problem solving electronic system activity pl ...

We are looking for people who are determined to make life better for people around the world. Support clinical trials by performing various tasks. · Work with internal departments such as medical affairs and external partners like CROs. · Cultivate scientific knowledge related to ...

This position is responsible for performing quality assurance tasks. The job involves verifying data completeness of manufacturing instructions and test records, changing the status of intermediate products and materials, inputting achievements, solving problems in warehouses and ...

+Job summary · The job involves creating and revising procedures for Lilly's Japanese GMP/QMS regulations and global quality standards. The specialist will also be responsible for training systems, managing them, and improving them. · +ResponsibilitiesCreate and revise procedure ...

Perform quality assurance tasks. Verify the completeness of manufacturing instruction records and test record data, change the status of intermediate products and materials, input achievements, resolve problems in warehouses and manufacturing areas, create activity planning recor ...

We unite caring with discovery to make life better for people around the world. · FUME Engineer responsible for maintaining troubleshooting operating facilities equipment including air conditioning compressors water supply systems electrical systems wastewater treatment systems e ...

The Safety Information Department at Lilly Japan is seeking a new team member to join their ranks as part of our graduate program. This role will involve working closely with other teams to ensure patient safety throughout all stages of drug development. · Collecting safety data ...

This job requires native level Japanese proficiency in writing reading and speaking. · ...

게이카 · 과 1야의 · 2026맑 13했어, · 쳴소러합록. · dental receptionist job · ...

We are looking for people who are determined to make life better for people around the world. · West Japan Manufacturing Site (Operations) · ...