Siemens PLC Engineer
صاحب العمل نشط
حالة تأهب وظيفة
سيتم تحديثك بأحدث تنبيهات الوظائف عبر البريد الإلكتروني
شارك هذه الوظيفة
حالة تأهب وظيفة
سيتم تحديثك بأحدث تنبيهات الوظائف عبر البريد الإلكتروني
الوصف الوظيفي
The ideal candidate must have knowledge of Design implementation and commissioning of S7 based Control Systems and/or Siemens TIA related software engineering activities for a variety of industrial control system
applications predominately in the Life Science industry. The candidate should have proven experience on PLC/SCADA/DCS systems ideally supported by Siemens certification and training.
Responsibilities:
Development of control system design and options for customer requirements.
Generate S88 based batch code.
Generate and execute test documentation & protocols as part of a cross discipline team.
Involvement throughout whole software/systems lifecycle from design through coding to testing
Installation and configuration and documentation. (Working throughout the full QA procedures)
S7 programming of control system from given designs and troubleshoot (PLC/DCS) software problems.
Raise and process change requests for hardware/software changes.
Qualifications:
B.S. degree in Engineering (Instrumentation/Electronics/Electrical/ Mechanical) or Applied Physics or similar.
Advanced knowledge & experience in Siemens Automation System Simatic S7 shall be preferable.
Minimum of 3 years SCADA Systems experience on Simatic S7 TIA & WinCC engineering testing and commissioning expertise is preferable.
Experience in Batch process (ISA S88 standard) Simatic Batch engineering testing and commissioning expertise is preferable.
Knowledge of GMP GAMP safety and environmental regulatory requirements
Good understanding of the production & utility processes (in particular Cleaning In Place)
Providing independent quality review and approval of system lifecycle documentation, such as plans, requirements, risk assessments, protocols and reports for new and modified systems. Providing independent quality review and approval of system changes. Supporting and approving computerised systems investigations and test deviations. Ensuring consistent approach to qualification, change and deviation management across systems being implemented on the project. Providing timely and pro-active QA IT support and guidance to facilitate project timelines, including close collaboration with the technical and business units. Where required, engaging with QA IT teams from other sites and capital projects to standardise and align approach to computerised systems compliance. Experience: Min. 5 years of experience in QA IT/CSV, CSV and/or a similar role in the pharmaceutical industry. Working knowledge of relevant regulations and industry standards. Proven ability to meet timelines, prioritise tasks and engage with stakeholders. Excellent communication skills. Project management experience will be an advantage. DeltaV
نوع التوظيف
دوام كامل
