Senior Automation Engineer

Sligo | Contract | www.cv-library.ie |
Senior Automation Engineer

Team Horizon is seeking a Senior Automation Engineer for a leading pharmaceutical company in Sligo.

Why you should apply:
 •  This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
 •  There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
 •  Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.

What you will be doing:
 •  Manage Automation projects throughout the project lifecycle.
 •  Provide technical support to all control system related issues. Tasks include, daily trouble shooting, optimisation, and documentation control.
 •  Leadership of control system validation activities during project start-up.
 •  Life cycle management of the on site control systems, to GAMP-4 requirements.
 •  Project management of control system elements of continuous improvement projects. Work closely with process engineers/ technical support chemists and other departments to deliver these continuous improvement projects.
 •  Project management and technical development of future integrations of the control systems, with planned MIS and ERP systems.
 •  Departmental budgeting as delegated by the Automation & IT Manager.
 •  Adheres to and supports all EHS & E standards, procedures and policies.
 •  To administer and support all Automation & IT Processes in Pharmaceutical Manufacturing environment.
 •  Implement, qualify, commission and maintain manufacturing Automation & IT systems (MES, SCADA) and associate IT infrastructure that delivers operational efficiency and agility.
 •  Identify, evaluate and implement opportunities for continuous Automation & IT process improvement.
 •  Define requirements on capital projects and interact with internal & external stakeholders, vendors and contractors.
 •  Work with Production/Engineering and Quality to troubleshoot and optimise output, minimise contamination and minimise costs.
 •  Generate & Maintain documentation (SOP’s & Technical Documentation) for full cGMP validation and operation, including documentation of changes made.
 •  Maintain Data Integrity Program, including remediation of legacy systems to ensure robust procedure and systems are in place covering data integrity, security and recovery.
 •  Actively Contribute to the Automation Business Strategy.
 •  Any other duties as assigned.

What you need to apply:
 •  Relevant 3rd level degree in Mechatronics, Electronics or Computer Technology.
 •  5-10 years’ experience in process automation, with relevant experience of batch processing and DCS platforms in a GMP environment in the pharmaceutical industry.
 •  3 years’ experience of the 21 CFR Part 11 requirements for automated systems in the pharmaceutical industry.
 •  3 years plus of Experience of plant start-ups and/or new product introductions to pharmaceutical facilities. Must be able to lead these activities in a start-up environment.
 •  Experience with PLC (Siemens), SCADA and process equipment. SCADA experience (iFix, WinCC).
Knowledge of Shop floor Network & Control Architecture with Electronic Batch Record Implementation. Instrumentation/Automation & Control knowledge with BMS / SCADA / DCS / PLC
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