DeltaV Lead Automation Engineer

Job title:

DeltaV Lead Automation Engineer

Company

Life Science Consultants

Job description

LSC have a great contract opportunity for a DeltaV Lead to join a top 10 Pharmaceutical company based in Tipperary. The site supports the complete pharmaceutical small molecule process for Phase III clinical to product release and market support. On site processes include API manufacture, formulation, OSD tableting, packaging and global logistics & distribution. The facility takes in raw chemicals and ships finished medicines to end users. This site has grown from an API site to a strategically important campus that supports critical stages of the company’s drug lifecycle.
If you have 5 years of experience working in a similar role in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you!ABOUT THE PROJECT – KEY RESPONSIBILITIES:

• As the DeltaV Lead 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.
• Develop and/or review SDLC deliverables, compliant with site 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. OEM automation systems, MES 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 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 functionsABOUT YOU – ARE YOUR SKILLS A MATCH?

• Minimum of 5 years’ experience in a similar role in the pharmaceutical industry
• Strong experience in the following systems: Emerson DeltaV incl. core system implementation, base layer, batch layer
• Knowledge of and experience with the following systems would be advantageous; Siemens PLC/SCADA, OSISoft PI, Werum Pas-X, ABB DCS or other DCS systems
• Hybrid working option is a possibility. 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)
• Relevant Computer Science or Engineering degree or equivalent
• Previous experience of API or OSD manufacturing will be advantageous
• Previous experience of high containment manufacturing will be advantageous

Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply!
Apply via this advert or contact Paul O’Driscoll at LSC on 021 4777329 if you have any more questions about this role!

Expected salary

Location

Tipperary

Job date

Sun, 04 May 2025 02:37:46 GMT

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