Position:OEM Automation Engineer. Location: Munster, Ireland.
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 experienced OEM Automation Engineer. This is a site-based role (3 days at site weekly on a hybrid basis).
Role Description
- Reporting to the Digital MMD Project Manager, part of workstream specifically responsible for OEM Automation Systems delivery.
- This candidate will be required to work closely with the Digital MMD teams responsible for the full Automation and IT scope and with vendors / partners with responsibility for delivery of systems.
Role Functions
Functions include, but are not limited to, the following:
- As an OEM Automation Engineer for the project, you will work with other Automation resources, Automation vendors and partners to deliver automation systems on time and within budget.
- Subset of scope may include: CMS guidance, partake in interface design and Digital MMD rep for any CMS integration with site CMS systems and upgrades engaging with Site DMO CMS SMEs.
- Develop and/or review SDLC deliverables, compliant with MSD 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. DCS and PI Historian.
- Work closely with the DDQ and CSV functions and ensure their requirements are met in all deliverables.
- Participate in Hardware and Software FATs and SATs to ensure company 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.
Role Requirements
- Degree qualification ideally in a related Automation, Engineering, Computer or other technical discipline.
- Strong experience in the following systems: Siemens PLC, SCADA and HMIs, Siemens TIA Portal.
- Minimum of 5 years' experience in a similar role in the pharmaceutical industry.
- Knowledge of and experience with the following systems would be advantageous: Simatic Logon, Siemens PM server, OSISoft PI, RT Reports, DeltaV.
- Hybrid working option is a possibility (3 days at site is required). The successful candidate may be required to attend periodic meetings or testing at vendor premises as required.
- Excellent computer skills, proficient in the use of the following Microsoft tools: Excel, SharePoint, Word and PowerPoint.
- Strong interpersonal and communication skills (verbal and written).
- Previous experience of Oral Solid Dose manufacturing will be advantageous.
- Previous experience of high containment manufacturing will be advantageous.
- Fluent in English, written and verbal.
- Must have valid EU Work Permit and Irish Residency
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