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Morgan McKinley

Project Engineer

Morgan McKinley

Tralee, County Kerry, Ireland · अनुबंध

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2 पहले
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नौकरी का विवरण

Job Overview

Become a key contributor within a prominent global pharmaceutical manufacturer committed to sustainability and societal welfare. In this role, reporting to the Engineering Projects & Systems Lead, you will be responsible for managing CAPEX and non-CAPEX engineering projects from conception through to final delivery. This position offers the chance to take full ownership of project timelines, budgets, and leading cross-functional teams within a forward-thinking and collaborative environment.

Key Responsibilities

  • Manage engineering projects comprehensively, including conducting feasibility assessments, defining objectives, scheduling, and allocating resources.
  • Oversee financial aspects, maintaining accountability for project budget and cash flow control.
  • Provide leadership by inspiring and directing both internal teams and external contractors or vendors.
  • Lead cGMP validation activities and prepare lifecycle documentation such as URS, FDS, FAT, SAT, IQ/OQ, and conduct Risk Assessments.
  • Support systems management by maintaining MES-managed documentation including System Configuration and Descriptions.
  • Ensure proper handover to business units under controlled conditions and perform post-project reviews to facilitate continuous improvements.

Candidate Profile

Essential qualifications and experience:

  • Experience in project engineering, management, or validation within pharmaceutical manufacturing settings.
  • Proven success in delivering engineering projects and equipment installations on schedule and within budget.
  • Strong financial understanding related to engineering project execution.
  • Comprehensive knowledge of project lifecycles from initial concept through to qualification phases.
  • Excellent communication, analytical, problem-solving, and time management abilities, capable of managing priorities in dynamic environments.

Preferred attributes:

  • Hands-on experience with drug manufacturing processes.
  • Exposure to cGMP start-up environments is advantageous.

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