Pharma Automation Project Engineer – GMP Upgrades

Hyper Recruitment Solutions Ltd

Waterford

On-site

EUR 65,000 - 90,000

Full time

14 days+

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Job summary

Hyper Recruitment Solutions Ltd in Waterford is seeking an Equipment Project Engineer - Automation to lead multi-phase automation upgrade projects in a GMP pharma setting, covering Lyophilisation, CIP, PMS, Autoclave and related control systems. You will coordinate with OEMs and internal teams to deliver compliant, on-time solutions.

The role requires a degree in engineering and a track record of 5+ years delivering complex pharma automation projects, CQV activities, and successful validation,

Qualifications

  • Degree or higher in engineering or a related technical field.
  • 5+ years delivering automation projects in pharma/biotech GMP environments.
  • Strong experience with OEM coordination, CQV activities, and server/control upgrades.

Responsibilities

  • Lead end-to-end automation upgrade projects, ensuring timely execution and quality standards are met.
  • Manage server, control system, and equipment deployments from initiation to completion.
  • Oversee FAT and SAT, along with documentation and change control processes.
  • Coordinate with OEMs and internal stakeholders to ensure GMP, GDP, safety, and regulatory standards.
  • Oversee project scheduling, budgeting, and multi-stakeholder communication.

Skills

Automation
Project management
GMP compliance
Regulatory compliance
CQV
OEM coordination
Validation
Team coordination
Budgeting

Education

Bachelor's degree in engineering

Tools

Siemens
DeltaV
PCS7
S7
TIAPortal
PLC
SCADA

Job description

Hyper Recruitment Solutions Ltd in Waterford is seeking an Equipment Project Engineer - Automation to lead multi-phase automation upgrade projects in a GMP pharma setting, covering Lyophilisation, CIP, PMS, Autoclave and related control systems. You will coordinate with OEMs and internal teams to deliver compliant, on-time solutions.

The role requires a degree in engineering and a track record of 5+ years delivering complex pharma automation projects, CQV activities, and successful validation,

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