製造マネージャー（横浜）

Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation.  At our core, we exist to create products that seek to improve the quality of life for people living with cancer and rare diseases.  You will be supporting the international roll-out of our approved prostate cancer imaging agent and helping us to advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases.

Telixでのあなたの未来を見てください

GMP（適正製造基準）、放射線安全規制、および企業の品質基準への準拠を確保する役割を担います。この職務には、生産スケジュールの管理、製造プロセスの最適化、規制遵守の確保、効率的かつ安全な業務の維持に向けたチームの指導が含まれます。

GMP、PMDA（医薬品医療機器総合機構）規制、放射線安全ガイドラインに準拠することを確保

CAPA）、継続的改善活動の管理

QA）および品質管理（QC）部門と連携し、製品の迅速な出荷を実現

GMP、放射線安全、業務手順に関する適切なトレーニングを実施

PMDA、ICH、PIC / S）への準拠を確保

SOP）、製造記録、逸脱報告などの正確かつ迅速な文書管理

GMP規制環境下での医薬品または放射性医薬品の製造における5年以上の経験

GMPまたは無菌操作に関する認証またはトレーニング

At Telix, we believe everyone counts , we strive to be extraordinary , and we pursue our goals with determination and integrity . You will be part of an engaged and supportive group of colleagues who all have a shared purpose : to help people with cancer and rare diseases live longer, better quality lives. Being a Telix employee means being a part of a unique, global, interdisciplinary team working to deliver what's next in precision medicine. We have hybrid and remote employees located all around the world. We offer competitive salaries, annual performance-based bonuses, an equity-based incentive program, generous vacation, paid wellness days and support for learning and development.

Telix Pharmaceuticals is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.

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