タロ 、 社 ： · ～HPLC.GC GMP ２GMP, · ３GMP４JAPAN JIS K 0104:2013 , · ...

· 品質管理部門にて、HPLCやGC、UVなどの分析機器を用いた理化学試験をお任せします。 · ・医薬品原薬の試験・検査、および記録確認(日本薬局方準拠) · ・薬学や化学分野のバックグラウンドをお持ちの方 · ...

+品質管理部における分析機器を使用した原薬の試験検査等の品質管理業務~日本薬局方にしたがった試験が主となります。 · +OOS、逸脱管理及び変更管理などの品質システムへの対応 · 新規原薬承認のための規格・試験法の設定や分析バリデーションの実施 · 将来的には部内のマネジメント・人的管理を担う~これらに付随する業務全般 · + ...

This position is located in Nagareyama City, Chiba Prefecture.We are looking for an Area Manager who will utilize their experience and skills to seek areas for improvement and lead various projects. · ...

We are looking for a Quality Assurance Engineer to join our team and contribute to the realization of high reliability and high quality through product assurance (PA) activities throughout the entire lifecycle of space systems. · ...

Takeda is a global values-based R&D-driven biopharmaceutical leader. We continue to innovate and drive changes that will transform the lives of patients. We're looking for like-minded professionals to join us. · ...

Takeda is looking for like-minded professionals to join us. We aim to create a diverse and inclusive organization where people can thrive, grow and realize their own potential while enabling our purpose. · ...

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 are a leading Global CRO Company providing drug discovery development lifecycle management and laboratory services. · We provide tailored solutions to ensure safety efficacy of clients' needs focused on compliance with strict regulations. · Clinical Trial Monitoring for Phase ...

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

We are seeking a Quality Control Inspector to join our team. As a Quality Control Inspector, you will be responsible for inspection and verification activities to ensure that products, components, and processes conform to applicable drawings, specifications, and quality requireme ...

+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) · ...

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

Astellas Pharma Co., Ltd. is looking for an Associate Manager SCM to contribute to the realization of its Vision by creating value from product creation to customer delivery through end-to-end supply chain management. · ...

We are looking for Area Managers who can lead projects and manage people with advanced technology and a "People First" mindset. · We are committed to trying things first. · We learn with curiosity. · ...

We are seeking Area Managers to lead projects and manage people with advanced technology and a “People First” mindset. · This is a position where you can advance your career even if you have no experience in logistics. Many people who have worked in completely different industrie ...

+ Job summary · As a Customer Quality Specialist at Johnson & Johnson, you will be responsible for ensuring the quality of our products and services. You will work closely with internal departments and external stakeholders to resolve customer complaints and improve product quali ...

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 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 ...

Are you ready to accelerate your potential and make a real difference within life sciences, · diagnostics and biotechnology? · ...