(Innovative Medicine) 生産物流本部 富士工場 製造部 ビジネスユニット3 マネージャー （富士工場）

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https : / / www.jnj.com Job Function : Supply Chain Manufacturing Job Sub Function : Manufacturing Product & Packaging Operations Job Category : People Leader All Job Posting Locations : Shizuoka, Japan Job Description : 主な職務及び主な責任 Major Job Duties and Responsibilities :

• In order to achieve goals of the entire Production department, they will work with director of the  department and also Head of Factory to secure necessary  resources to achieve the goals and to work / collaborate with other departments.
• KPIとの関連性を全員に周知する。 Be familiar with overall operations in each business unit and ensure that everyone in their team is aware of the relationship between goal setting and the KPIs.
• KPIを達成するため、グループ内のシニアスーパーバイザー及びスーパーバイザーと定期的にレビューを行いながら、安全で安定した品質の製品をスケジュール通りに生産することの全般を担う。 Hold periodical reviews with Senior Supervisors and Supervisors internally to achieve KPI  for his / her BU and take ownerships of producing products with safe / stable quality as scheduled.
• OEE（Overall Equipment Effectiveness）改善目標達成のための必要なサポートを行う。 Do exemplary actions in the Kaizen-proposal activity for inspection / packaging and for safety operations, and be a good role model for the performance and also support the actions to achieve the Target OEE for entire team.
• Share the team’straining plan with the Supervisors and handle issues and whole action plans.
• GMP / CGTP遵守のため、各種決められたトレーニングを各ビジネスユニット全員が期日通りに完了できるようにプラン、サポートする。 Develop a plan and give support for the teammembers completing any training by due date to follow the GMP / CGTP requirements.
• Actively connect with all BU members, support their career development, and proceed with the operations considering Work-Life Balance.
• Make sure giving  support to the supervisors regarding root cause investigation and action plan development when any deviation or quality issues occur.  Being responsible for the outcome of the correction / preventive actions.
• Deliver strong value of  Safety, Quality, Reliability, and Cost in the Plant. 法規制の順守に関する責任 Regulatory Compliance Responsibilities :
• GMP / CGTPおよび全ての会社 / サイトのポリシー / 手順を遵守すること。 Production Manager should follow GMP / CGTP, and all company / site policies / procedure.
• Must concern compliance as high priority. 教育 / 経験Education and Experiences :
• University / Bachelor’s Degree or equivalent.
• Process Excellence or Project Management experience. 知識、資格、及び技能 （必須）Knowledge / Certification / Skills (Must) :
• Business Level of English (Once / week tele conference regarding system error or new production implementation process etc)
• 5-10年の類似の業務経験 Generally requires 5-10 years relates experience.
• Min 2 years or more experience either at frontline position in Production or Quality or Demand / Supply Planning.
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