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新着求人 生産技術  (MF-134)
募集職種 外資系製薬企業の Reliability Manager
その他のGMP生産管理・技術の求人はこちら
勤務地 埼玉
会社概要 非公開
求人要件 【職務内容】
【役割と責任】
The Manufacturing Division consists of 2 manufacturing departments, IPT-1(solid dosage mainly) & IPT-2(vaccine & sterile mainly). Reliability Engineering(RE) department belongs to IPT-1, but accountable to support both 2 IPTs and Logistics team in order to drive stability for product supply to customers/patients by providing professional maintenance & daily trouble shooting. The RE department covers all manufacturing process (Formulation, Inspection, Packaging, Warehousing) and accountable for new manufacturing process installation in some cases.
The position requires passion, energy and strong leadership as well as technical Manufacturing expertise & management process. And expectations to be;
Set clear Vision & Strategy for RE team aligning with IPT’s/Site’s and drive results
Drive GEMBA Centric Culture with daily KAIZEN/interactions collaborating with all operations/support functions
Drive operational excellence, identify and support Operational improvement activities and mindset with healthy unsatisfactory in status quo
Drive personal operational ownership and accountability for all operators and Teach and Coach operators to improve their skillset for timely & proper trouble shooting
Manage & Develop Reliability Engineering staffs & develop high performance team
The position has 9 direct reports including 1 senior engineer. Travel could be 10% or less.
【代表的な業務】
Provide technical/professional support on daily trouble shooting & improvement to all Manufacturing operations and implement professional maintenance for the site manufacturing process.
Ensure Manufacturing Efficiency without compromising Compliance & Safety.
Prioritize Maintenance related risks, and develop and assist with implementing corrective and preventive action plans. Monitor and communicate overall status of plans to IPT-1 Lead/Site Management.
Proactively identify improvement opportunities and collaborate with Operations/ Logistics/ Engineering/and Quality/EHS personnel to leverage best practices and drive continuous improvement efforts.
Ensures that maintenance programs are in place to maintain 100% GMP compliance.
Provide technical support for new projects and modifications to ensure proper design review, as well as routine /maintenance evaluation after process / equipment installed / implemented.
Conduct periodical Professional maintenance with venders.
Manage budget for RE expense related to Maintenance and Head Count in the team.
応募資格 【必要とする資質】
Technical related Bachelor's degree
Previous experience in leading project teams with and/or without managerial responsibility is advantageous
Clear and recognizable understanding of the processes, equipment and methods
Proven ability to develop sustainable cooperative professional relationships on all levels of the organization
Excellent communication, interpersonal, and organizational skills
High ethical standards, being a role model of business compliance and integrity
Proven ability to prioritize, focus on and obtain business results
Demonstrated analytical and logical problem solving abilities
Flexibility to perform multiple, complex tasks simultaneously to efficiently support the business
Fluency in written and spoken in both Japanese and English
【望ましい資質】
Business Acumen
Relevant professional certification(s) in Manufacturing, Safety or Quality
Lean/Six Sigma experience desirable
Robust skills interpreting and applying regulatory frameworks such as EU OSHA, OHSAS 18000, EPA, ISO, NFPA, ICH/GMP related etc.
Pharmaceutical company experience is not mandatory if there is Manufacturing, Engineering or Maintenance program experience, and may fit with FMCG or automobile company experience. Lean Six Sigma or KAIZEN activity lead experience is strongly preferred.
募集背景  
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