募集要項
- 募集背景
- 増員
- 仕事内容
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●Interface with site operation owners to collect and analyze key data related to various site performance indicators
●Establish and provide consistent timely analysis and publication of key quality metrics. Perform trend analysis in collaboration with site operation owners to forecast preventative actions
●Schedule, facilitate and assist in the execution of the Site Quality Council meetings. Compile and authorize meeting agenda items, minutes and the Quality Council Dashboard
●Identify critical quality issues along with risk associated with supply chain, drug shortages and new product launches and escalate to the Global Governance Council
●Track the resolution deliverables with respect to identified quality performance indicators
●Prepare and deliver presentations and detailed analysis results to Global Governance Council and/or senior management, including regular status updates and reports
●Advice for improvement of quality control system and solution of analytical issue
- 応募資格
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- 必須
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【Required Knowledge/Skills and Abilities】
* Quality control experience (analysis experience) in the pharmaceutical industry or any other business field where GMP practice/knowledge is applied
* Management skill
【Preferred/Required Experience】
* Pharmacist Qualification
* Knowledge of manufacturing process in the pharmaceutical industry
* Good communication, understanding, decision-making skills
* Ability to work efficiently, cooperate well and broad view point
【Language】
* Business Level English
【Education】
* Minimum of a Bachelor's degree (Pharmacy or Chemistry)
- 歓迎
- -
- 募集年齢(年齢制限理由)
- 25歳～40歳 （特定年齢層の特定職種の労働者が相当程度少ないため）
- フィットする人物像
- -
- 雇用形態
- 正社員
- 勤務地
- 埼玉県川越市
- 勤務時間
- 8：45～17：15
- 年収・給与
- 経験・能力を考慮
- 待遇・福利厚生
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社会保険完備、退職金制度（確定給付＋確定拠出）
育児・介護休職制度、福利厚生「ベネフィット・ステーション」加入
- 休日休暇
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土・日（完全週休2日制）、祝日
年末年始（7日）、夏期休暇（3日）、年次有給休暇（初年度4～11日、次年度11日、最高20日）、
病気休暇（初年度1～5日、次年度以降6日）
年間休日126日（2011年）
- 選考プロセス
- ※新しい情報を掲載しておりますが、万が一募集を締め切っている場合もございますので予めご了承下さい。
