Remote Equipment Project Lead - Pharma GMP Upgrades

Hyper Recruitment Solutions; Waterford; On-site; EUR 65,000 - 95,000; Full time

Job summary

Hyper Recruitment Solutions is seeking an Equipment Project Engineer (Production Equipment) to lead key equipment and facility projects in Co Waterford. You will manage initiatives from initiation to completion in a highly regulated biopharma setting, supporting production upgrades, CQV activities and GMP-compliant operations to ensure smooth manufacturing processes.

Based remotely with a focus on project delivery, you will oversee project governance, risk management, and documentation control

Qualifications

• Degree or higher in Process, Mechanical, Chemical, Industrial, or related Engineering.
• 5+ years leading engineering projects in pharmaceutical or biotech GMP environments.
• Strong knowledge of GMP/GDP, validation lifecycle, cleanroom standards, and aseptic processing.
• Experience with production equipment upgrades, facility projects, and CQV processes.

Responsibilities

• Manage end-to-end project delivery including scope, schedule, cost, safety, quality, and compliance.
• Lead design reviews, ensuring alignment with URS, GMP/GDP, and regulatory standards.
• Coordinate with contractors, OEMs, and internal stakeholders to ensure accurate and timely delivery.
• Oversee procurement processes, equipment acceptance, documentation, and change control.
• Support CQV activities including FATs, protocol reviews, and qualification documentation.
• Maintain project governance, reporting, and documentation control to support audit readiness and regulatory compliance.

Skills

Project management

GMP knowledge

CQV

Regulatory compliance

Facility upgrades

Education

Engineering degree (Process/Mechanical/Chemical/Industrial)

Job description

Hyper Recruitment Solutions is seeking an Equipment Project Engineer (Production Equipment) to lead key equipment and facility projects in Co Waterford. You will manage initiatives from initiation to completion in a highly regulated biopharma setting, supporting production upgrades, CQV activities and GMP-compliant operations to ensure smooth manufacturing processes.

Based remotely with a focus on project delivery, you will oversee project governance, risk management, and documentation control