技術系（機械設計・製造技術） - 設備保全・メンテナンス・施設環境・安全衛生
技術系（機械設計・製造技術） - プラントエンジニア（電気）
技術系（機械設計・製造技術） - プラントエンジニア（機械）
技術系（機械設計・製造技術） - プロセスエンジニア（プラント）

■Job Description Summary
Site Engineering Lead RLT is responsible for developing strategies and implementing Engineering activities in line with Sasayama Site and Novartis Manufacturing & Supply business objectives. This is a key role for Sasayama RLT Operations LT

■Job Description
MAJOR ACCOUNTABILITIES
・Ensure all facilities, utilities and equipment are designed and operated in a safe and effective manner and are compliant with applicable standards
・Lead innovation and reliability for Sasayama RLT operations
・Support / implement Global Engineering initiatives and projects in Sasayama (ALCM, Standards, Best Practice Networks, Automation, Project Roadmap etc.).
・Work closely with RLT Project Director and Campus Engineering Head to control and deliver major projects ensuring project objectives of scope, cost and schedule are maintained.
・Develop facilities and equipment recapitalization plan for Sasayama RLT
・Ensure that all facilities and equipment are designed and implemented fit for purpose operating standards, develop early asset management strategy during the project phase
・Support / Lead cost for unit and operational efficiency initiatives for RLT Sasayama
・Be part of the site RLT Ops leadership team that leads competitiveness journey to achieve long term performance
・Ensure that process and equipment technology used in operations is consistent with product needs and people capability
・Ensure sustainable internal operations through effective asset risk control and timely recapitalization of site assets to match product needs and ‘Fit for Purpose’
・Consistently apply a standard asset maintenance strategy across Divisions, to maintain design working conditions, reduce breakdowns and increase equipment life cycle
・Develop / implement necessary organizational structure inline with global blueprints and campus dynamics
・Manage baseload capital projects after site operations
・Develop site qualification / commissioning plans and support site validation master plan

■休日：完全週休二日制, GW, 夏季休暇, 年末年始

■Requirement:
・7+ years of general engineering experience thereof +5 years’ experience in a pharmaceutical manufacturing environment specifically in the manufacturing of aseptic, radiopharmaceutical or customized medicine
・Outstanding Technical knowledge with demonstrated ability to deliver safe and fully compliant technical solutions
・Demonstrated Leadership abilities leading a team aligned around business/technology/project processes
・Well-developed communication skills, able to present com-fortably to Senior Management and to Technical experts
・Demonstrated with knowledge/understanding of key non-technical business processes, Human Relations, Finance
• Advanced HSE and GxP/QA knowledge.
・Business acumen, understanding value chain of manufacturing and applying risk based / fit for purpose solutions.
・Degree in engineering (Dipl. Ing. or M.Sc. or B.Sc.) or equivalent
・Fluent in English and Japanse essential, others helpful

■職種未経験者：不可