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PACIV, a global leader in industrial automation solutions with offices in Ireland, the United States and Puerto Rico, and serving the Life Science, F&B and Utilities industries, is looking for an Projects Automation Engineer.  This is a site-based role.

Job Description

This role is a Projects Automation Engineer working within a multinational life science manufacturing environment in Dublin Ireland.

• Responsible for Automation and IT Systems delivery as part of ongoing LifeCycle Management process

• This candidate will be required to work closely with the AIT and LifeCycle Management teams responsible for the full Automation and IT scope and with vendors / partners with responsibility for delivery of systems.  

  Responsibilities of the Role

• As the Automation Engineer for the Project Team, you will work with other Automation resources, Automation vendors and partners to deliver automation systems on time and within budget.

• Develop and/or review Software Development LifeCycle deliverables, compliant with Company standards, including but not limited to:

• Requirements Specifications

• Requirements Traceability Matrix

• Functional Specification

• Design Specification

• Code Review

• Test specification/test script

• Etc.

• Work closely with vendors of Automation equipment to ensure deliverables meet project requirements, including the interfacing of new Automation equipment with existing site systems, incl. MES and PI Historian.

• Work closely with the QA-IT and Computer Systems Validation functions and ensure their requirements are met in all deliverables.

• Participate in Hardware and Software FATs and SATs to ensure MSD requirements and standards are met.

• Follow project schedules and document trackers to assist in the management and control of project deliverables.

• Participate in Automation meetings and support relevant program meetings.

• Liaise with stakeholders on the overall project to ensure clear communication between all parties.

• Ensure Automation compliance with Global Policies, Procedures and Guidelines, regulatory requirements and execute current good manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions.

• Comply with Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions.

• Work collaboratively to drive a safe and compliant culture

  Requirements

  Core Competencies (Technical):

• Strong experience in the following systems: Siemens and Rockwell PLC, SCADA and HMIs.

• Knowledge of and experience with the following systems would be advantageous; Siemens Desigo BAS, Siemens PM server, OSISoft PI, RT Reports, FTView, FactoryTalk.

• Some knowledge of Computer System Development Lifecycle is preferred

• Proficiency in Microsoft Office and job related computer applications required

• Prior experience in a similar role in the Pharmaceutical industry is desireable

• Candidates must have a valid EU Work Permit and Irish Residency

  Core Competencies (Business):

• Effective communication and interpersonal skills to interface effectively with all levels of colleagues in a team environment

• Self-motivated

• Effective time management and multi-tasking skills

• Problem solving skills

  Qualifications:

• Degree Qualification ideally in a related Automation, Engineering, Computer or other Technical discipline

  Compensation

• Regular staff position, competitive salary and employee benefits package.

• Job type: full time.

• Job location: site-based role in Dublin Ireland.

   

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