+注射製剤試験スタッフ+ · ++ 実施(ADC原薬、ADC製剤、一般無菌製剤、特薬無菌製剤、異物分析等の調査対応) · ...

注射剤製造設備の維持・管理、空調設備の維持・管理、機械設備の知識、経験、電気設備の知識、経験、製薬用水設備の知識、空調設備の知識、経験、製薬会社でエンジニアリングの経験がある方、IT、DX技術を活用した生産効率改善の経験 · 機械設備の知識、経験 · 電気設備の知識、経験 · 製薬用水設備の知識 · 空調設備の知識、経験 · 製薬会社でエンジニアリングの経験 · IT、DX技術を活用した生産効率改善の経験 · 注射剤製造設備の維持・管理 · 空調設備の維持・管理 · 機械設備の知識 · 電気設備の知識 · 製薬用水設備の知識 · 空調設備の知識 · エン ...

微生物試験スタッフの仕事は、製薬用水のサンプリング、水質試験、製造現場の環境検出菌の同定業務の実施、医薬品の無菌試験、バイオバーデン、原料の生菌数試験業務の実施、滅菌器の滅菌バリデーションや培地性能試験の実務業務の実施です。 ...

+注射剤製造スタッフ · ・注射剤製造オペレーション · +・製造指図・記録作成(製造実行システム使用) · + ...

製薬用水のサンプリング、水質試験及び製造現場等の環境検出菌の同定業務の実施・医薬品の無菌試験及びバイオバーデン、原料の生菌数試験業務と滅菌器と培地性能試験を担当します。 · 5~10年以上経過した微生物试验业务經驗 · ...

Clinical Research Associate monitors patient data and research-related information at clinical research sites and clinical trials. Investigator provides input to data validation plans in accordance with research protocols, regulatory requirements, and good clinical practices. Pro ...

Monitor patient data and research-related information for clinical research sites and clinical trials. Provide input to data validation plans and offer investigation-related information as needed from source documents, research records, and site visits. Monitor the selection of i ...

Principal Safety Evaluation is responsible for ensuring the safety of products and patients throughout the product lifecycle. This includes conducting cross-functional activities to support the development of GSK Japan's projects, designing and implementing safety plans for clini ...

+Job summary · The role involves achieving sales targets in designated areas. · +ResponsibilitiesDemonstrate clinical scientific knowledge about disease mechanisms of targeted products. · Provide business plans reflecting market principles affecting product sales. · ...

You will be responsible for achieving sales targets in your designated area. You will also need to have expertise in product adaptation diseases mechanisms of action which you must demonstrate through clinical scientific knowledge. · You will need to have an MR qualification hold ...

FP&A and Reporting Manager job opening at a biotech company in Tokyo. The company is developing innovative treatments for cancer and is looking for a skilled FP&A professional to lead the annual budgeting, quarterly forecasting, and long-term financial planning processes. · Lead ...

This is a Manager, Medical Customer Care GMT Business Unit position at Alexion Japan. The job involves working with medical professionals and being the primary point of contact for Alexion. The role requires building good relationships with medical professionals, providing custom ...

Internal Audit Manager to lead audit activities in Japan, focusing on US-SOX compliance. Develop and execute annual audit plans, including US-SOX compliance audits. Design and improve audit methodologies aligned with J-SOX where applicable. Evaluate and document internal controls ...

Internal Audit Manager is responsible for leading internal audit activities in Japan, focusing on US-SOX compliance. The role involves developing and improving the internal audit and control system, designing and improving audit methodologies, and evaluating and documenting inter ...

The CAI Japan team is looking for individuals with a variety of experience in Commissioning Qualification Validation (CQV) production facilities equipment pharmaceutical medical device biotechnology industry. · Lead project team site execute Commissioning qualification validation ...

We are looking for a Senior CQV Project Manager to join our CAI Japan team. The ideal candidate will have experience in commissioning, qualification, and validation (CQV) of production facilities and equipment in the pharmaceutical/medical device/biotechnology industry. ...

We may use artificial intelligence (AI) tools to support parts of the hiring process. · This Senior CQV Engineer role at CAI involves commissioning , qualification and validation documentation. · The candidate should have 5-12 years experience performing commissioning activities ...

CAI is looking for an individual with a range of experience in the areas of commissioning, qualification, and validation to join our team in Japan. Experience in the pharmaceutical, medical device or biotechnology industries is required. · Commissioning, qualification, and valida ...

The primary role of the Customer Service Engineer will focus on installs, repairs, maintenance, validation and qualifications of multi-vendor equipment at customer site. The engineer will provide scheduled and unscheduled corrective maintenance for customers including warranty se ...

Se busca FP&A e informes gerenciales en una empresa biofarmacéutica internacional con sede en Japón. · ...

Somos una empresa biotecnológica internacional en proceso de IPO. Estamos buscando un gerente de auditoria interna para apoyar nuestro crecimiento. · ...