ジョブNo.780892 Site Quality Lead, Senior Director Quality

  • 正社員
  • 外資系企業
  • 従業員1000名以上
  • 年間休日120日以上
  • フレックスタイム

非公開

• 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.

ワークライフバランスの良さや、社内(国内外)での豊富なキャリアパスが用意されている点が特徴のグローバル企業です。

コンサルタント 成田 卓

募集要項

職種 メディカル系/医薬品質保証(QA)(製造所)
年収 1600万円~2400万円
勤務地 滋賀県
応募資格 • Experience working within cross functional and global teams
• Track record of working with regulatory health authorities/ stakeholders/ government bodies / industry associations
• Has managed significant risk, and has experience in applying robust judgement in high profile and high-pressure situations
• Has experience in change, budget and project management
• Proven track record of attracting and developing talent, building capability and driving performance in direct and matrixed leadership roles
• Extensive work experience and deep understanding of culture(s) in Japan market
• Familiarity with the regulations in Japan

薬剤師
学歴 大卒以上(理系学部)
雇用形態 正社員(期間の定めなし)
勤務時間 09:00-17:15
[実働時間] 7時間15分
内勤:フレックスタイム制有
休日・休暇土、日、祝日
年間休日 125日
夏季休暇、年末年始休暇、育児休暇、介護休暇、慶弔休暇
慶弔、赴任、リフレッシュ他
待遇・福利厚生社宅、従業員持株制度、財形貯蓄、その他待遇・福利厚生
【諸制度】社宅制度、厚生年金基金、退職年金、財形貯蓄、融資制度、持株会制度、慶弔見舞金、マルティプル・エンプロイメントシステム、AZストックボーナス、ほか 【その他】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
健康保険、厚生年金、労災、雇用保険
通勤交通費(全額)、営業手当、住宅手当
受動喫煙防止措置敷地内禁煙

企業情報

企業名非公開
業種・資本 メーカー系(医薬品(メーカー))
ヘッドオフィス:海外

Site Quality Lead, Senior Director Quality

  • メディカル系/医薬品質保証(QA)(製造所)
  • 1600万円~2400万円
  • 滋賀県