PACIV, a global leader in industrial automation solutions with offices in Ireland, the United States, and Puerto Rico, serving the Life Science, F&B, and Utilities industries, is looking for a 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:
o Requirements Specifications
o Requirements Traceability Matrix
o Functional Specification
o Design Specification
o Code Review
o Test specification/test script
o 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 desirable.
* 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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