Detalii job :

OEM Automation Engineer

  • AA Euro Recruitment Ireland
  • Nedeterminata
  • Medical Farmacie
  • Dublin, Irlanda
  • 4 EUR
  Cere sa fii sunat

Descriere:

OEM Automation Engineer - Dublin

Summary:
As a member of the Operations IS Automation team, the role will support complex and challenging system automation initiatives.

Responsibilities:

• Ownership and administration of equipment control systems in a GMP regulated manufacturing setting.
• Support Drug Product manufacturing within the Formulation, Vial/Syringe Filling, Lyophilisation, Component Preparation and Packaging areas.
• Lead and support system improvements, development of detailed specification, engineering documents, and standard operating procedures.
• Lead technical root cause analysis, incident investigations and troubleshooting issues related to electrical, instrumentation and equipment control systems.
• Support new product introductions or new technology introductions by performing engineering assessments, implementing automation system configuration changes and supporting engineering runs.
• Solving complex problems, project management, lifecycle management and operational excellence.
• Develop and manage change control requests per established SOPs and processes.
• Support a safe working environment by complying with all pertinent environmental health/safety practice, rules and regulations.
• Travel at various times may be required to support execution of projects.

To apply please send your CV on jordan.anghel@aaeurorecruitment.com

Cerinte:

Qualifications:
• Bachelors in Electrical Engineering or Computer Science, Chemical Engineering, Biotech Engineering or related life science engineering.
• 5+ years’ experience in operations/manufacturing environment
• Manufacturing automation experience in biopharmaceutical Formulation/Fill/Finish or Active Pharmaceutical Ingredient (API) facilities.
• Have an awareness of process software modelling tools.
• Excellent control systems automation background focused specifically in design, installation, programming, validation and lifecycle maintenance of automated equipment specifically in the areas of Formulation, Vial/Syringe Filling, Lyophilisation and Packaging.
• Experience with Rockwell Automation PLC/SCADA/Batch, Siemens PLC/HMI, iFix, Wonderware, Elau/Kinetix Motion Control, ControlNet, DeviceNet, Profibus.
• Knowledge of GAMP software development lifecycle & 21 CFR Part 11.
• Experience in change control, non-conformance, corrective and preventative actions, and validation practices.
• Ability to influence the development of business area strategy and IT strategy where appropriate.
• Development and presentation of project plans to senior management.
• Able to multi-task in project environments and skilled in communication and collaboration Team player.
• Prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making.