求人・転職情報
2件中の1〜2件を表示
グラクソ・スミスクライン株式会社
仕事内容
■Job Purpose
Provide leadership, technical expertise and support for the new products introduction at site through product trasfers from sister sites, 3rd party contract manufacturer or developed branded generics to ensure that new products are manufactured site on time and in full. Work closely with Global MSAT team, engaging appropriate Subject Matter Experts (SME) support as required to rapidly resolve technical problems and improve products and processes.
■Key Responsibilities
1. Strategic Planning
Own core technical business processes for site: Product Lifecycle Management (Technical Risk Assessment, Product Control Strategy, Continued Process Verification, Process Robustness Assessment), New Product Introduction and Technical Transfer to/from other sites/ 3rd party contract manufacturer / developed branded generics, Change Control and Risk Management.
Contribute to strategic planning, based on those above and business continuity initiatives to support long-term site development.
Support technology transfer and automation efforts while preparing engineering teams for effective planning and execution.
2. Operational Business
Support product control strategy translation to shop floor (batch instruction, standard work etc), utilizing the principles of GPS with matrix leadership across Engineering, VS, Quality and Logistics.
Ensure product life cycle management, including NPI processes - technical risk assessment activities to ensure critical to quality attributes in the processes are identified and managed, product performance – solving technical issues through DMAIC and CAPA implementation, and risk management – monitoring technical standards and identifying risks.
Delivery key process improvement/optimization projects that contribute to site KPIs: cost of goods, process robustness, cost of poor quality, yield and waste to continue to improve site competitiveness.
3. Compliance and Procedural Implementations
Ensure MSAT owned processes and ways of working are up to dated to provide efficient, effective and compliant technical support to values streams.
Accountable and responsible for continues process verification, process transfer, process validation / PPQ, cleaning validation, trouble shooting / RCA, process mapping, change control, process improvements, statistics, technical standards and process science.
Support site quality / EHS and business plans, drive continuous EHS and quality improvements, monitor performance metrics, and ensure alignment with global GSK policies and guidelines.
4. People Management & Development
Ensure effective staff selection, training, and development to maximize potential and meet business goals, while empowering FLL and SMEs to make informed decisions.
Lead by example through strong leadership behaviors and utilize performance development plans to drive team growth and performance.
Provide leadership, technical expertise and support for the new products introduction at site through product trasfers from sister sites, 3rd party contract manufacturer or developed branded generics to ensure that new products are manufactured site on time and in full. Work closely with Global MSAT team, engaging appropriate Subject Matter Experts (SME) support as required to rapidly resolve technical problems and improve products and processes.
■Key Responsibilities
1. Strategic Planning
Own core technical business processes for site: Product Lifecycle Management (Technical Risk Assessment, Product Control Strategy, Continued Process Verification, Process Robustness Assessment), New Product Introduction and Technical Transfer to/from other sites/ 3rd party contract manufacturer / developed branded generics, Change Control and Risk Management.
Contribute to strategic planning, based on those above and business continuity initiatives to support long-term site development.
Support technology transfer and automation efforts while preparing engineering teams for effective planning and execution.
2. Operational Business
Support product control strategy translation to shop floor (batch instruction, standard work etc), utilizing the principles of GPS with matrix leadership across Engineering, VS, Quality and Logistics.
Ensure product life cycle management, including NPI processes - technical risk assessment activities to ensure critical to quality attributes in the processes are identified and managed, product performance – solving technical issues through DMAIC and CAPA implementation, and risk management – monitoring technical standards and identifying risks.
Delivery key process improvement/optimization projects that contribute to site KPIs: cost of goods, process robustness, cost of poor quality, yield and waste to continue to improve site competitiveness.
3. Compliance and Procedural Implementations
Ensure MSAT owned processes and ways of working are up to dated to provide efficient, effective and compliant technical support to values streams.
Accountable and responsible for continues process verification, process transfer, process validation / PPQ, cleaning validation, trouble shooting / RCA, process mapping, change control, process improvements, statistics, technical standards and process science.
Support site quality / EHS and business plans, drive continuous EHS and quality improvements, monitor performance metrics, and ensure alignment with global GSK policies and guidelines.
4. People Management & Development
Ensure effective staff selection, training, and development to maximize potential and meet business goals, while empowering FLL and SMEs to make informed decisions.
Lead by example through strong leadership behaviors and utilize performance development plans to drive team growth and performance.
求める経験 / スキル
■Basic Qualification
>Skill
・Pharmaceutical Operation Knowledge / Presentation & Communication / Computer Skills / Report Writing / Problem Solving
・Overall Pharmaceutical Experience of 7+ years
・Management experience of workforce with direct and functional affiliations to execute operations
・Well acquainted with EHS and GMP Standards and their implementation
・Understanding of budgeting and expenditure processes
・Detailed knowledge of relevant dosage form including unit operation understanding, functionality, and criticality of formulation materials and their transofmration (e.g. powder technology, colloid science, isolation, drying and particle size reduction), plant equipment and analytical testing.
・Able to assess/interpret statistical data; e.g. process capability, control charts, DoE, MSA.
・Knowldege of Japan market regulatory environment.
・Interaction with other community (outside of Imaichi) and also with other engineering leads
>Experience
・8-12 years minimum experience in manufacturing processes / pharmaceutical industry, with a minimum 5 years managerial experience
・Education/certification/Language
・Bachelors degree in Pharmacy or Chemical Engineering or equivalent in an appropriate business / technical area( Scientific, Technical, Engineering )
・English skill : Business level
>Preferred Qualification
・Education/certification/Language
・Post graduate degree ( Scientific, Technical, Engineering )
*Future scope of job and working location will be determined
>Skill
・Pharmaceutical Operation Knowledge / Presentation & Communication / Computer Skills / Report Writing / Problem Solving
・Overall Pharmaceutical Experience of 7+ years
・Management experience of workforce with direct and functional affiliations to execute operations
・Well acquainted with EHS and GMP Standards and their implementation
・Understanding of budgeting and expenditure processes
・Detailed knowledge of relevant dosage form including unit operation understanding, functionality, and criticality of formulation materials and their transofmration (e.g. powder technology, colloid science, isolation, drying and particle size reduction), plant equipment and analytical testing.
・Able to assess/interpret statistical data; e.g. process capability, control charts, DoE, MSA.
・Knowldege of Japan market regulatory environment.
・Interaction with other community (outside of Imaichi) and also with other engineering leads
>Experience
・8-12 years minimum experience in manufacturing processes / pharmaceutical industry, with a minimum 5 years managerial experience
・Education/certification/Language
・Bachelors degree in Pharmacy or Chemical Engineering or equivalent in an appropriate business / technical area( Scientific, Technical, Engineering )
・English skill : Business level
>Preferred Qualification
・Education/certification/Language
・Post graduate degree ( Scientific, Technical, Engineering )
*Future scope of job and working location will be determined
従業員数
2,500名
(2025年1月時点)
勤務地
栃木県
想定年収
1,200 万円 ~ 2,000 万円
従業員数
2,500名
(2025年1月時点)
株式会社足利銀行
仕事内容
・ビジネス戦略を考慮した全行的なセキュリティ方針・戦略の策定・管理、ロードマップの作成・リスク評価
・セキュリティ対策基準の策定、セキュリティシステムの計画策定、対策状況の分析・見直し
・技術的なセキュリティ対策の動向調査
・セキュリティインシデント(事件事故)管理
・セキュリティに関する経営層への報告
・行員向けセキュリティ教育・意識向上の推進
・取引先へのセキュリティ高度化コンサルティング
■特徴・魅力
・銀行業務において、システムは不可欠であり、そのリスク管理は非常に重要な役割を担っています。システムを安定的に導入・運用することで地域のお客さまの利便性に貢献でき、ご自身のスキルとノウハウを如何なく発揮できるやりがいのある業務です。
・サイバー攻撃からお客さまの資産や情報を守ることで、お客さまの安心・安全な生活の維持に寄与することができます。
・セキュリティ対策基準の策定、セキュリティシステムの計画策定、対策状況の分析・見直し
・技術的なセキュリティ対策の動向調査
・セキュリティインシデント(事件事故)管理
・セキュリティに関する経営層への報告
・行員向けセキュリティ教育・意識向上の推進
・取引先へのセキュリティ高度化コンサルティング
■特徴・魅力
・銀行業務において、システムは不可欠であり、そのリスク管理は非常に重要な役割を担っています。システムを安定的に導入・運用することで地域のお客さまの利便性に貢献でき、ご自身のスキルとノウハウを如何なく発揮できるやりがいのある業務です。
・サイバー攻撃からお客さまの資産や情報を守ることで、お客さまの安心・安全な生活の維持に寄与することができます。
求める経験 / スキル
■以下のご経験をお持ちの方を歓迎します。
・金融機関を対象としたサイバーセキュリティに関するコンサルティング業務や全社的な計画立案・管理業務の知見・経験のある方。
・セキュリティ対策に当たっては、「ビジネス戦略」「ユーザー利便性」と「費用」と「リスク」のバランスを取り、関係部署と意見を調整したうえで対策の立案ができる方。
■必要資格・スキル
・情報処理安全確保支援士
■あれば望ましい資格・スキル
・システム監査技術者
・金融機関を対象としたサイバーセキュリティに関するコンサルティング業務や全社的な計画立案・管理業務の知見・経験のある方。
・セキュリティ対策に当たっては、「ビジネス戦略」「ユーザー利便性」と「費用」と「リスク」のバランスを取り、関係部署と意見を調整したうえで対策の立案ができる方。
■必要資格・スキル
・情報処理安全確保支援士
■あれば望ましい資格・スキル
・システム監査技術者
勤務地
栃木県
想定年収
1,000 万円 ~ 2,000 万円
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職種から求人を探す
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業種から求人を探す
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勤務地から求人を探す
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年収から求人を探す
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