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Automation Project Manager - Digital Integration

Real
Posted 4 days ago, valid for a month
Salary

£60.43 - £77.69 per hour

Contract type

Full Time

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Sonic Summary

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  • Real Life Science is seeking an Automation Project Manager for a contract role in Grangecastle, Ireland, with a duration of 6-12 months and potential for extension.
  • The role involves leading multiple automation and digital integration projects in a regulated pharmaceutical environment, ensuring delivery on scope, schedule, budget, and quality.
  • Candidates must have 5+ years of project management experience within pharmaceutical or biopharma environments and a strong knowledge of automation/control systems, preferably with Yokogawa experience.
  • Key responsibilities include managing project documentation, overseeing commissioning and validation activities, and ensuring compliance with industry standards.
  • This position offers competitive contract terms and the opportunity to work on high-impact projects in a global pharma setting.


Automation Project Manager - Contract Role (Pharma)

Location: Grangecastle, Ireland (Hybrid)

Duration: 6-12 months (potential extension)

Real Life Science is currently recruiting an Automation Project Manager for a global pharma manufacturer based their Grangecastle site. The Automation Project Manager will lead multiple automation and digital integration projects within a regulated pharmaceutical environment.



Key Responsibilities

  • Manage automation and digital integration projects across the site, ensuring delivery on scope, schedule, budget, and quality.
  • Lead major initiatives including:
    • Installation of an offline DCS control system for training/validation.
    • Upgrade of Yokogawa DCS software and OT network infrastructure.
    • Replacement of legacy control systems and lifecycle upgrades.
  • Act as primary liaison with automation, IT/OT, and control system vendors.
  • Drive integration of plant automation with manufacturing OT/IT systems for data integrity and performance management.
  • Prepare and manage project documentation: URS, design specs, RFPs, risk assessments, and business cases.
  • Oversee FAT/SAT, commissioning, qualification, and validation activities.
  • Ensure compliance with GMP, 21 CFR Part 11, Annex 11, and company standards
  • Coordinate training and handover to operations and support teams.


Requirements

  • 5+ years' experience in project management within pharmaceutical or biopharma environments.
  • Strong knowledge of automation/control systems (DCS/PCS/SCADA - Yokogawa experience desirable).
  • Proven ability to manage full project lifecycle: feasibility, design, vendor selection, implementation, and handover.
  • Familiarity with OT network infrastructure, system security, and data integration concepts.
  • Excellent stakeholder management, communication, and leadership skills.


Why Join?

  • Work on high-impact automation projects in a global pharma environment.
  • Collaborate with cross-functional teams and cutting-edge technologies.
  • Competitive contract terms with potential for extension.

Please click here to find out more about our Key Information Documents. Please note that the documents provided contain generic information. If we are successful in finding you an assignment, you will receive a Key Information Document which will be specific to the vendor set-up you have chosen and your placement.

To find out more about Real, please visit (url removed)

Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 8 Bishopsgate, London, EC2N 4BQ, United Kingdom | Partnership Number | OC(phone number removed) England and Wales

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