Biopharma Equipment Project Lead: GMP/CQV, 12m Contract

Hyper Recruitment Solutions Ltd; Waterford; In loco; EUR 65.000 - 90.000; Tempo pieno

Descrizione del lavoro

Hyper Recruitment Solutions Ltd is seeking an Equipment Project Engineer (Production Equipment) to lead and deliver key equipment and facility projects within a highly regulated biopharmaceutical environment in Co Waterford. The role focuses on production upgrades, CQV activities, and GMP-compliant operations to ensure smooth manufacturing processes.

The role is a 12-month contract with potential extension, requiring a degree in engineering and experience in GMP environments.

Competenze

• Degree or higher in Process, Mechanical, Chemical, Industrial, or related Engineering discipline.
• Experience leading engineering projects in pharmaceutical or biotech GMP environments; ~2–3 years post graduation.

Mansioni

• 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 for audit readiness and regulatory compliance.

Conoscenze

Project management

Biopharma GMP

CQV

Regulatory compliance

Formazione

Process/Mechanical/Chemical/Industrial Engineering degree or higher

Descrizione del lavoro

Hyper Recruitment Solutions Ltd is seeking an Equipment Project Engineer (Production Equipment) to lead and deliver key equipment and facility projects within a highly regulated biopharmaceutical environment in Co Waterford. The role focuses on production upgrades, CQV activities, and GMP-compliant operations to ensure smooth manufacturing processes.

The role is a 12-month contract with potential extension, requiring a degree in engineering and experience in GMP environments.