Project Engineer, Manufacturing & Validation

Abbott Laboratories

Killybegs

On-site

EUR 70,000 - 100,000

Full time

3 days ago
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Job summary

Abbott Ireland Diabetes Care Division Donegal is seeking a qualified professional to develop and conduct project plans and validations to meet site goals. You will support manufacturing performance through expertise in equipment, processes and materials.

The role involves leading validation protocols, data analysis and reporting, and contributing to CAPA investigations. A science/engineering degree and 4+ years of relevant experience are required, with a focus on GMP and continuous improvement

Qualifications

  • Third level qualification in Science or Engineering.
  • 4+ years relevant experience preferred.

Responsibilities

  • Create, identify, plan and conduct medium to large-size projects with risk-managed execution.
  • Generate and execute validation protocols, trials and reports for equipment, test methods, processes and materials.
  • Ensure validation reports are generated, executed and reviewed for related activities.
  • Lead analytical process development through design and execution of experiments.
  • Perform data analysis, evaluate results, and contribute to improvements.
  • Support investigations and CAPAs in quality and process areas.
  • Manage data, trends (including SPC) and reporting of product performance.
  • Complete documentation timely according to business standards.
  • Understand and comply with EHS policies and GMP requirements.
  • Identify opportunities for new technology and drive continuous improvement.
  • Perform other duties as assigned.

Skills

Project management
Validation execution
Data analysis
Documentation
Quality systems (GMP)

Education

Bachelor's degree in Science or Engineering

Tools

SPC (Statistical Process Control)

Job description

Abbott Ireland Diabetes Care Division Donegal is seeking a qualified professional to develop and conduct project plans and validations to meet site goals. You will support manufacturing performance through expertise in equipment, processes and materials.

The role involves leading validation protocols, data analysis and reporting, and contributing to CAPA investigations. A science/engineering degree and 4+ years of relevant experience are required, with a focus on GMP and continuous improvement

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