Automation Engineer IV
Novo Nordisk
- 天津市
- 长期
- 全职
Accept ClosePress Tab to Move to Skip to Content LinkSearch by KeywordSearch by LocationLoading...Category×Select how often (in days) to receive an alert:×Select how often (in days) to receive an alert:Automation Engineer IVCategory: Digital & ITLocation:Tianjin, Tianjin, CNAre you motivated by driving innovation for the life-changing benefit of patients? Are you ready to help transform the treatment paradigm for a broad range of chronic diseases that currently rely on injection-based therapies? Then this is your moment. Apply now and join Novo Nordisk. Together we can create life-changing innovation. Together we can make it happen.The position
- In close collaboration with global program team, vendor and local project team, focusing on Automation system design and implementation. Ensure high-stability and leading automation technology for process intend use for continuously production after FFEx facility is live.
- Automation technical solution review, monitoring and risk control in technology point of view. Escalating the risk to stakeholder in advance, to ensure all of automation system risks mitigating to acceptance and meet the project quality and schedule.
- Effective Communication with stakeholders, including local project members, venders and headquarter. Ensure transparent of project status
- Execute validation process in project progress, take the Automation technical expert responsibility, responsible for technology support and document review and approval in complete validation lifecycle.
- Responsible for one or more areas in AP process or Facility process, fully support from project initiation to production.
- Automation tech. work: including design review, FAT, Commissioning, SAT, IOV, PfV, PV and ramp-up, responsible for recover and fix malfunction and keep improvement in whole project progress. Management for technical document and punch-list/open issue list, to ensure project assets completely and technical issue traceability
- Validation work: including document review and approval in different phase of project, handling automation relevant VDV and tests, ensure completely and effective validation to establish and maintain validated state of automation system.
- Communication work: ensure effective communication with all stakeholders.
- Continue to share technology and experience and maintain FFEx STJ automation knowledge base.
- Actively initiate continued improved automation system to meet the requirement of system stable, safe and high efficiency running; Root cause analysis and PM/CM action setting up by Lean thinking and tools, create and maintain automation related operational procedure documentation, such as OPL, SOP.
- Technical support of different engineering disciplines in project upgrade and have right competence in external vendors, minor projects management, validation process competence and GMP audit/inspection readiness
- A bachelor/master's degree in Automation /Computer Science and technology/ Information Technology/Electrical Engineering/AI or other relevant engineering majors
- GMP background: 3+ years manufacturing experience in pharmaceutical automation systems of cGMP/GAMP regulated pharmaceutical industry or in life science industry preferable
- Automation experience: 5+ years experience in automation Designing, commissioning, validation, Process Improvement and operation, especially in Formulation/Filling/Wash & Sanitation/Inspection/Clean Utility/BMS/FMS relevant process.
- Proven experience with the operation, maintenance and optimization of IT/PLC/PCS systems. Additionally, we hope that you can have most of following: knowledge of PLC systems, SCACA system, servo system, MES, industrial communications, SQL, VB/C/java program language, Specific knowledge about Siemens PLC/SCADA solutions.