エージェント取り扱い求人

Automation Electrical Engineer, Japan New Plasma Facility Project

募集中
  • 勤務地
    大阪府
  • 職種
    その他製剤化/製造・生産関連職
  • 業種
    医薬品メーカー(先発医薬品)

募集要項

業務内容 OBJECTIVES/PURPOSE
Responsible for designing, developing, and maintaining electrical and automation systems. The successful candidate will work closely with cross-functional teams to ensure that all electrical and automation systems are in compliance with regulatory requirements and industry standards.

Project engineering for the Strategic Automation Pillars in the areas of:

Automation Security & Integrity Engineering
Automation & Control Systems Data Integrity
Automation Cybersecurity
Automation Solutions & Systems Engineering
Functional setups & architectures of systems & components
Supervisory Control Structures & Data Mgt.
Automation Data Engineering
Standard Automation Integration Layer (Shopfloor Systems & Data Integration)
Data Channels, HMI, displays & Visuals
Historization
Automation Data Governance Engineering
Data Structures & Contextualization
Use Case Owner Liaison Mgt, Technical2Business (and vice versa) translation
ACCOUNTABILITIES
As a member of the Engineering workstream of the project, provides guidance and leadership to all automation-related activities in accordance with the Global Automation Strategy. In detail, He/she will:
Report to the engineering manager.
Develop and maintain automation guidelines and standards based on project approved budget and schedule, and ensure compliance
Ensure that all automation systems meet regulatory requirements, client specifications, and industry standards and define the user requirements.
Ensure compliance with Automation Standard Requirement Specification, Automation Engineering Guideline, compliance, and cybersecurity in the project.
Collaborate with other project disciplines to ensure integrated design solutions.
Guide and coordinate with external design company the procurement strategy packages definition related to its discipline.
Review and approve automation documents and concepts.
Conduct gate keeping reviews.
Review and approve contractor submittals.
雇用形態 正社員
応募資格 Bachelor`s or Master’s degree in Automation Engineering (process, data, equipment, facility automation), or Electromechanical/Chemical/Electronics/Electrical Engineering with the main subject of Automation Engineering (process, data, equipment, facility automation).
Chief electrical engineer certification (電気主任技術者) – Type 3 – ECEE
Minimum of 5 years of experience in engineering in a pharmaceutical, biotech or similar manufacturing environment.
Experience in projects with different integrated processes.
Design and develop electrical and automation systems.
Ensure that all electrical and automation systems are in compliance with regulatory requirements and industry standards.
Troubleshoot and resolve electrical and automation issues in a timely manner.
Develop and maintain automation and electrical documentation, including schematics and wiring diagrams.
Collaborate with cross-functional teams to ensure that all electrical and automation systems are integrated with other manufacturing systems.
Participate in the installation, commissioning, and validation of electrical and automation systems.
Provide technical support to manufacturing and maintenance teams.
A proven track-record in electrical and automation systems and data integration.
Strong knowledge of proven industrial electrical and automation technologies and experience in emerging (Industry 4.0) technologies & how to apply these in pharmaceutical concepts.
Strong cybersecurity knowhow & industrial networking experience.
Strong knowledge of electrical systems and equipment, including PLCs, HMIs, and motor controls.
General knowledge in Digital/Data Science and its enabling concepts.
Data Integrity Trouble Shooting & GxP knowledge, good pharmaceutical and/or integrated manufacturing processes experience and knowledge.
High Project management skills & Strong Financial acumen.
Result-driven
Business fluent proficiency in English and Japanese (written and oral).
Strong skills to work in matrix organization with excellent interpersonal, communication, influencing, and negotiation skills required.
Solid industry knowledge, project proficiency, and autonomy expected.
Demonstrate strong communication skills to effectively communicate with all levels of professionals, both internal and external.
Ensure and be accountable for all deliverables, including schedule milestones, financial performance, and quality of scope according to the assigned projects.
Manage contractors and external vendors to deliver robust technical solutions.
Manage and forecast capital and expense budgets.
英語力 問わない
年収 500万 〜 800万円
給与詳細 500万円-800万円
勤務地 大阪府
備考 ”Better Health for People, Brighter Future for the World” is the purpose of a company.We aim to create a diverse and inclusiveorganization where people can thrive, grow and realize their own potential while enabling our purpose. We continue to innovate and drive changes that will transformthe lives of patients. We’re looking for like-minded professionals to join us.
global values-based, R&D-driven biopharmaceutical leader. We are guided by our values of ism, whichhas been passed down since the company’s founding. ismincorporatesIntegrity, Fairness, Honesty, and Perseverance, with Integrity at the core. They are brought to life through actions based on Patient-Trust-Reputation-Business, in this order.

企業情報

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OBJECTIVES/PURPOSE Own Process Equipment is “fit for purpose” for the manufacture of drug substance and drug products, meeting Regulatory, Quality, Capacity and EHS requirements Main objectives (key services) Technology selection Capacity Modeling and Site Master Planning Engineering and Equipment Design Safety engineering design and management “Factory Floor” Continuous Improvement/ Troubleshooting / System ownership Own strategic preparation of sites for the future by introducing new process technologies such as robotics and delivering agile process engineering solutions Provides leadership to all engineering disciplines during the development of the project requirements, scope, design (concept, basic, and detail), timeline, and budget# The incumbent is responsible for improving existing equipment to minimize production downtime and provide leadership to all process equipment related investigations Develop and implement strategies to ensure cost and time effective designs while ensuring innovation and adhering to user requirements while managing daily operational support ACCOUNTABILITIES Technology selection Drive Cross functional stakeholder management with our Partners in Manufacturing e.g. Sciences and/or Pharmaceutical Sciences. 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Total Cost of Ownership (TCO) calculations Manage Process Equipment Vendors and Architectural/Engineering firms in the delivery of CAPEX and OPEX projects in areas of responsibility Capacity Modeling and Site Master Planning Mentoring of Process Unit Operation Capacity models and identify capacity bottlenecks / constraints in GMP manufacturing processes / production process and in the utilities delivery systems Apply knowledge of heat transfer, mass transfer, fluid dynamics, reaction kinetics to solve common process engineering problems Engineering and Equipment Design Own Front-End Engineering and Design activities in feasibility study and conceptual design phases Sponsor Project Turnover Packages for Process Equipment are delivered to site and that critical engineering knowledge such as as-built drawings, operating and maintenance manuals, equipment and instrument data sheets, spare parts lists are maintained, remain accurate and up to date Gather requirements from Stakeholders - such as from Quality, Manufacturing, Reliability, Maintainability, Automation, and EHS – to decide on Process Basis of Designs, specifications and designs for Process Equipment, Process Control Systems, Process Instrumentation and Process Safety Systems and Devices Lead Scope of Work and RFx Packages for Process Equipment Vendors, Process Engineering Consultants, Architectural / Engineering services, Commissioning services and (Sub-) Contractors Sponsor commissioning activities such as Factory Acceptance and/or Site Acceptance Testing of process equipment With Partners in Engineering Validation mentor the Qualification and Validation activities for Process Equipment SME Design Reviews of Process Equipment with Stakeholders, including Quality, Manufacturing, Utilities Operations, Maintenance, Calibration, Reliability, Automation Safety engineering design and management Conduct Process Hazard Analysis (e.g. PHA-Hazop) of hazardous manufacturing / production processes and incorporate improvements into the design of process equipment, process control, and process safety systems Perform Design Reviews of all process equipment with relation to EHS and lead for the relevant changes Own Investigations for process equipment and implement Corrective and Preventive Actions (CAPA) “Factory Floor” Continuous Improvement/ Troubleshooting / System ownership Provide leadership the Manufacturing and Maintenance departments with troubleshooting activities of Process Equipment on the factory floor Owner continuous improvement activities for Process Equipment applying continuous improvement tools such as DMAIC, FMEA, RCA, identify improvements, design and implement improvements and sponsor 3rd level troubleshooting in collaboration with “Manufacturing” &” Manufacturing sciences” Mentor Management of Change for Process Equipment in area of responsibility Responsible for internal and regulatory Audits and Inspections Engage in the Process Engineering Community of Practice (CoP) through sharing of best practices and lessons learned DIMENSIONS AND ASPECTS Technical Expertise: Lead and mentor system/equipment specifications Determine basic causes, and develop and then follow up on recommendations for corrective actions Enable capabilities to perform troubleshooting on system/equipment Lead customer service problems and recommend design improvements Leadership: Displays and drives culture of -ism, PTRB, safety, and quality into the organization Be on the floor to study and train and recommend techniques to enable the team to improve existing equipment to minimize production downtime. 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