
【米原工場】Site Quality Lead, Senior Director Quality
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求人No. 182582
募集要項
業務内容 |
• Leads Quality function in a manner that maximises its contribution to the achievement of business objectives, profitability and return on investment. May have direct contribution to achievement of objectives across AstraZeneca more broadly. • Ensure that roles, responsibilities and reporting lines are clearly defined throughout the organisation, to assure a functionally independent quality unit. • Ensure sufficiently trained resources with adequate product and process knowledge for execution of GMP/GDP obligations and on-going professional development to maintain proficiency. • Ensure continuing suitability and effectiveness of the quality management system, product quality and GMP/GDP compliance through management reviews and through advocating continuous improvement. • Is responsible for ensuring that the requirements and implications of all applicable external regulations and the AstraZeneca Quality Management System and Code of Ethics are understood and effective implementation processes are put in place in all parts of the business area for that is responsible for. • Has technical oversight and responsibility for the quality and GMP/GDP compliance approaches and outcomes into the operations business area. • Is responsible for ensuring the professional development of the organisation in order to provide sufficient qualified resources and strong succession pipeline for site quality function and wider network. • Is responsible for ensuring that AstraZeneca is involved with and influential in key external organisations and events that interact with the government agencies that oversee and regulate the pharmaceutical development, manufacture and quality systems for medicines within Japan. • Is responsible for the Management review process and outputs for the site and for ensuring appropriate management focus on quality and compliance topics affecting Japan Operations business. • Leads the Quality elements of change programmes and projects in their site, working with the business to prioritise delivery of the Global Quality strategy. • Optimises key relationships with organisations (e.g. external regulatory bodies and Quality networks) to take full advantage of efficiencies and meet compliance obligations. • Works in partnership with the business and specialist Quality colleagues to ensure that an environment of continued professional development is created and individual and team performance is managed effectively. |
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語学力 |
要 |
年収 |
1300万~1951万 |
給与 |
月給制 ※ご本人の経験・能力・前給等を考慮し、規定により優遇します。 |
雇用形態 |
正社員 |
勤務地 |
滋賀県 |
休日 |
年間休日125日 ■完全週休2日制 (土日) ■祝日休み ■年末年始休暇 ■慶弔休暇 ■有給休暇 ■産前・産後休暇 (取得実績あり) ■育児休暇 (取得実績あり) ■介護休暇 (取得実績あり) ■リフレッシュ休暇 ほか |
福利厚生 |
各種社会保険完備 ■社会保険完備(雇用・労災・健康・厚生年金) ■社宅制度(適応の場合) ■財形貯蓄制度 ■融資制度 ■持株会制度 ■慶弔見舞金 ■健康診断 ■福利厚生倶楽部 ■リスクベネフィット(特別弔慰金、入院見舞金及び治療給付金、災害補償) ■退職金制度 ほか <諸手当> ■通勤手当 ■住宅手当 ■単身赴任手当 ■休日手当 ■営業日当 など <研修制度> ■入社時導入研修 ■MR認定試験対策研修 ■製品研修 ■MRセリングスキルUP研修 ■管理者研修(コーチング、ビジネスマネジメント、ピープルマネジメント、リーダーシップほか) ■部門別スキルアップ研修 ■通信教育 ■英会話研修 ほか |
企業情報
事業内容 |
医療用医薬品の開発、製造及び販売 |
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業種分類 |
メディカル/医薬品メーカー |
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