PLC/SCADA Engineer
Waterford | Contract | www.cv-library.ie |
We’re recruiting for a PLC/SCADA Engineer to work on an initial 12 month contract based in Ireland.
ROLES AND RESPONSIBILITIES
• Contribute to the completion of projects, manage your own time to meet agreed targets and develop plans for short-term work activities on your own projects.
• Developing automated system life cycle documents to meet cGMP requirements (i.e. SOPs, Configuration Specifications, Functional Design Specifications).
• Supporting department audit/inspection readiness and participate in audits and regulatory inspections as required.
• Ensure that work performed is accurate, timely, efficient and compliant with corporate policies, Good Manufacturing Practices regulations, and Regulatory Agency requirements.
• Must be solutions orientated, delivery focused with a strong technical background.
• Implementing code/systems changes on the automation systems under change management/change control as part of sustaining and Capital projects as required.
• Working on production systems continuous improvement initiatives.
• Maintaining the validated state of the automation systems.
• Any other activities as directed by the Area Lead.
SKILLS AND EDUCATION
• Third level qualification in Electrical, Electronic, Systems Engineering, Computer Science or Equivalent
• 3+ years’ experience working with automated control systems preferably in the Life Sciences/ Pharma or Medical Device sectors
• Excellent communication skills
• PLC/SCADA/HMI experience with preference for following technologies: Siemens PLC/HMI
• Knowledge of GAMP software development lifecycle, S88/S95 industry standards and 21 CFR Part 11
HOW TO APPLY
If you're interested in this role, click 'Apply Now' to forward an updated copy of your CV
ROLES AND RESPONSIBILITIES
• Contribute to the completion of projects, manage your own time to meet agreed targets and develop plans for short-term work activities on your own projects.
• Developing automated system life cycle documents to meet cGMP requirements (i.e. SOPs, Configuration Specifications, Functional Design Specifications).
• Supporting department audit/inspection readiness and participate in audits and regulatory inspections as required.
• Ensure that work performed is accurate, timely, efficient and compliant with corporate policies, Good Manufacturing Practices regulations, and Regulatory Agency requirements.
• Must be solutions orientated, delivery focused with a strong technical background.
• Implementing code/systems changes on the automation systems under change management/change control as part of sustaining and Capital projects as required.
• Working on production systems continuous improvement initiatives.
• Maintaining the validated state of the automation systems.
• Any other activities as directed by the Area Lead.
SKILLS AND EDUCATION
• Third level qualification in Electrical, Electronic, Systems Engineering, Computer Science or Equivalent
• 3+ years’ experience working with automated control systems preferably in the Life Sciences/ Pharma or Medical Device sectors
• Excellent communication skills
• PLC/SCADA/HMI experience with preference for following technologies: Siemens PLC/HMI
• Knowledge of GAMP software development lifecycle, S88/S95 industry standards and 21 CFR Part 11
HOW TO APPLY
If you're interested in this role, click 'Apply Now' to forward an updated copy of your CV
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