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  • 29 Mar 2019

    リライアビリティ マネージャー/Reliability Manager

    Japan

    Permanent Position
    MSD - グローバルヘルスケアリーダーMerck & Co., Inc., Kenilworth, N.J., U.S.A.の一員として、日本の皆さまに医療用医薬品やワクチンをお届けし、革新的なヘルスケア・ソリューションを提供しています。強固なパイプラインと世界140カ国以上で事業を展開するグローバルなネットワークを活かし、未だ満たされていない日本の医療ニーズに積極的に応えていきます。

    Job Description

    【役割と責任】
    The Menuma 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.

    Expires on 28 Apr 2019

    Posted By

    PSJ HC (少しでも、ご興味お持ちの方はお気軽にご連絡ください。 事前に職務経歴書(英語版、日本語版でも可)を 表記のメールアドレスまでご送付いただけますとスムーズです。)

    Tel: 080-1118-4497

    psj_hc@pplesearch.com

    Requirements

    【必要とする資質】
    Technical related Bachelor's degree or equivalent knowledge
    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. 


    給与:前職考慮のうえ決定します。

    勤務地:妻沼工場(埼玉県熊谷市)

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