デスタ · 私 · HPLC · GC · analysis machine）！ · （ HPLC · ...

（self-service） · ％ ＇ ６ · ...

研究職、医薬品(製剤)、原薬の理化学試験、製薬用水試験、手順書の作成、分析装置の維持管理 · 医薬品(製剤)及び原薬の品質試験・安定性試験経験がある方歓迎 · ...

品質管理業務 · *検査部品の検査業務 · *パソコン業務 · *お客様・協力会社の対応 · *事務処理 · *外注先との打ち合わせ · ...

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静岡で高い着工数を誇る木造戸建住宅の施工管理全般です。 · 1棟1棟異なる、デザイン性の高い住まいを最高の品質に仕上げるお仕事です。 · ...

+当社のソフトウェア開発における品質管理や品質向上に関わる業務をしていただくメンバーを募集します。ニコン共に様々な製品開発を進めていくことで社会に貢献する一端を担うことができます。 · +平均所定労働時間(1か月当たり):170時間 · +ソフトウェア開発経験(設計、プログラミング、テスト)3年以上 · ...

We are seeking a Quality Assurance/Control Specialist to join our team at Boehringer Ingelheim Corporate. As a key member of our quality assurance team, you will play a crucial role in ensuring high-quality products reach customers safely and effectively. · You will be responsibl ...

We're looking for a Principal Specialist to join our QARA team in Tokyo. As a General Marketing Supervisor under the PMD Act, you'll ensure compliance with all applicable QMS and GVP requirements. · ...

The company is seeking a Quality Assurance Technical Service Specialist to handle the following responsibilities: Product-related collaboration with manufacturing contractors · Technical transfer and maintenance management of products · This role requires experience in CMC-relate ...

The main responsibilities of this role include ensuring compliance with GQP Ordinance regulations by creating SOPs for drug products. · ...

This is a summary of the job. · Supervise document control defined in GQP Ordinance (SOP, Quality Standard Codes)Release products to market ensuring manufacturing control and quality control are appropriately assessed Investigate and analyze quality problems of products before s ...

Perform GXP activities according to GQP/GMP Ministerial Ordinance and GDP guideline. · SUPVISE DOCUMENT CONTROL DEFINED IN GQP ORDINANCE · ...

+Job summary · The GXP Quality Assurance Specialist will oversee all aspects of quality assurance in accordance with regulatory requirements. · +ResponsibilitiesSUPervise document control defined in GQP Ordinance (SOP Quality Standard Codes) · ...

The Quality Manager will support the international roll-out of our approved prostate cancer imaging agent and help advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases. · ...

Telix Pharmaceuticals seeks Quality Manager to oversee manufacturing quality control management at its Japanese facilities. This role ensures compliance with Japanese regulatory requirements (PMDA Ministry of Health Labour Welfare JNMT) The main responsibilities include: GMP(適正製造 ...

Takeda is a global values-based, R&D-driven biopharmaceutical leader. We are guided by our values of Takeda-ism, which has been passed down since the company's founding. Takeda-ism incorporates Integrity, Fairness, Honesty, and Perseverance. · ...

Takeda is looking for a Manager to join their Pharmaceutical Sciences team in Fujisawa. · We aim to create a diverse and inclusive organization where people can thrive, grow and realize their own potential while enabling our purpose. · We're seeking like-minded professionals to j ...

By clicking the "Apply" button I understand that my employment application process with Takeda will commence. Below are key points about this role: · We're looking for like-minded professionals to join us. · Takeda is a global values-based R&D-driven biopharmaceutical leader. · ...

+調剤薬局での受付事務全般:レセコン入力、レセプト作業および付随する業務・調剤補助業務を担当します。+ · +レセコン入力、レセプト作業および付随する業務・調剤補助業務を担当します。 · ...

The Quality Assurance Assistant will be responsible for translating and proofreading documents, as well as conducting customer service tasks by phone or email. The ideal candidate should have basic computer skills, experience with translation software and AI tools, and the abilit ...