Capital Projects Engineer – Pharma/MedTech

Powerflow Electronics Ltd.; Connacht; Presencial; EUR 65.000 - 90.000; Jornada completa

Descripción de la vacante

The Power Group Ltd. is seeking a Project Engineer for a County Mayo-based role within its Capital Projects Team.

You will deliver a diverse portfolio of engineering projects including equipment upgrades, process improvements, and facility enhancements in a regulated manufacturing environment. You will lead multidisciplinary teams, manage documentation, and coordinate internal resources and external vendors to ensure projects meet safety, quality and GMP standards while staying on schedule and

Formación

• Third level qualification in an Engineering or equivalent discipline/experience.
• Experience of working in Biologics, Pharmaceuticals or Medical device industry. For a minimum of 3 years experience.
• Project Engineering experience for a minimum of 2 years.
• Proven track record of delivery of projects in a Multinational Organisation.
• Must uphold GMP standards and safety on site.

Responsabilidades

• Develop and maintain project plans including resource requirements, cost phasing, schedules and production forecasts.
• Lead multidisciplinary engineering teams to ensure on-time, within-budget project delivery and quality.
• Coordinate Change Controls, Risk Assessments, Validation Protocols and Validation Reports.
• Manage external vendors and contractors to meet project requirements and timelines.
• Monitor risks and dependencies, implement mitigation plans and report progress to stakeholders.
• Prepare tender packages and evaluate vendors based on capability and cost.
• Track project expenditure and create phased costing plans.

Conocimientos

Project management

Leadership

Communication

Teamwork

Initiative

Educación

Third level engineering qualification

Descripción del empleo

The Power Group Ltd. is seeking a Project Engineer for a County Mayo-based role within its Capital Projects Team.

You will deliver a diverse portfolio of engineering projects including equipment upgrades, process improvements, and facility enhancements in a regulated manufacturing environment. You will lead multidisciplinary teams, manage documentation, and coordinate internal resources and external vendors to ensure projects meet safety, quality and GMP standards while staying on schedule and