募集職種

管理者・施設長  

雇用形態

正社員

仕事内容

This position is responsible for the management of his/her team, and has the following principal accountabilities as an area supervision/technical resource/technical Subject Matter Expert (SME). ・Manage the quality system of analysis for semi-finished products and final products. ・Build the quality system based on the Global Audit, Site Quality plan, and GQS/LQS requirements. ・Extend Japanese high quality level to the other sites by effective communication. ・Manage team staff and support to get the opportunities to increase the advanced skill and the GMP knowledge. ・Certify team members to perform each role. ・Review and approve site QC testing/inspection results, deviations, changes, Analytical Investigation report for invalidated OOS/OOT per procedure. ・Review and approve site QC technical documents as appropriate. Safety, Quality, Compliance & Service ・Always pay attention to and proactively participate the Health, Safety and Environment (HSE) related activities in order to achieve zero serious incident and fatality. ・Provide guidance and consultation to others for HSE improvement. ・Manage and control overall system of analytical test for semi-finished products and final products. ・Understand the GMP/QMS and the Pharmaceutical Affairs Law, and educate the subordinates to handle in an appropriate manner. ・Gain sufficient technical/transferable skill, provide solutions for technical problems and operational support to team members. Process & Operational Excellence ・Serve as QC Process Team Leader to ensure safety, quality, capacity and execution excellence. ・Communicate with global/local counterparts to solve problems and enhance Operational Excellence. ・Lead projects for compliance, efficiency, operational excellence and/or optimization. (e.g., lean, global/local projects, lab equipment recapitalization, new products launch preparation) ・Make sure all required activities are planned and executed, such as equipment periodic maintenance or stability program. ・Maintain the validated state of analytical method and equipment following method transfer and/or equipment qualification. ・Identify and implement process improvements to continually enhance the quality of the operations, workflow, and procedures. People, Organization & Others ・Communicate with team members periodically to work properly, and provide appropriate supports and opportunities for team members' development and career planning. （One-on-One / Performance Management /Development plan etc.） ・Develop staffs that have the technical/transferable skill and confirm the training records. ・Reexamine and adjust human resource/equipment capacity periodically to build more systematic and more highly qualified team. ・As site QC Lead Team member, develop and implement strategic plan, manage and control team expense and resource.

給与

正社員：年収 10,000,000円〜

給与の備考

年収　　1000万円～　経験により応相談

待遇・福利厚生

通勤手当：有 寮・社宅：有 住宅手当：有 宅援助制度、借上社宅制度、グループ補償制度（医療費・歯科医療費補助制度等）カフェテリアプラン制度

試用期間

6ヶ月

勤務時間

通常（実質労働時間との連動） 就業時間：00:00 ～ 00:00 交代制 3 交代制勤務 (1)7:00-15:45 (休憩 12:00-13:00) (2)14:00-22:45(休憩 19:30-20:30) (3)22:30-07:15 (休憩 2:30-3:30)

休日

年間休日数：125 完全週休2日制 年間有給休暇：入社月の区分に従い入社の翌月1日に付与　10日 ～ 20日 法定休暇：年次有給休暇 特別休暇：夏季休暇、年末年始休暇 その他休暇：慶弔

応募要件

・Bachelor’s degree in a scientific area or health care field ・Knowledge/Experience of analytical testing (Chemical and/or Micro-biological and/or Biological testing), analytical method transfer, and lab equipment ・Strong oral and written communication skills in Japanese and English ・Strong ability of people management, operation management, project management, problem solving, influence others and stakeholders without direct positional authority

最終更新日：2026/4/14

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