Biopharma Project Engineer - Process Equipment & Validation

Regeneron

Limerick

On-site

EUR 46,000 - 88,000

Full time

7 days ago
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Job summary

Regeneron is seeking a Project Engineer to join our Project Engineering team in Raheen, Limerick. You will design and specify cGMP process equipment, manage small projects, and assist in design reviews, installations, and validations.

Ideal candidates hold a BS/BEng or higher in Chemical/Process/Mechanical engineering with 2+ years of related experience, with direct biopharmaceutical equipment exposure preferred. On-site role offering growth in a fast-paced, regulated environment.

Qualifications

  • BS/BEng or higher in Chemical/Process/Mechanical engineering with 2+ years of related experience.
  • Direct experience with biopharmaceutical process equipment is preferred.
  • May substitute relevant experience for education.

Responsibilities

  • Designing and specifying cGMP process equipment, piping, and/or controls.
  • Managing small projects related to process equipment and manufacturing.
  • Assisting in the design review, site acceptance and installation of equipment.
  • Preparing process and instrument drawings and other related drawings.
  • Developing Process Flow Diagrams for manufacturing processes.
  • Supporting the validation department by preparing design documents and assisting in protocol execution.
  • Assisting in investigations of process equipment and control system anomalies.
  • Implementing corrective/preventative actions for existing equipment and manufacturing processes.
  • Preparing engineering evaluations for and executes modification change control documentation.
  • Supervising mechanical, electrical, and automation contractors.

Education

BS/BEng or higher in Chemical/Process/Mechanical engineering
2+ years of related experience

Job description

Regeneron is seeking a Project Engineer to join our Project Engineering team in Raheen, Limerick. You will design and specify cGMP process equipment, manage small projects, and assist in design reviews, installations, and validations.

Ideal candidates hold a BS/BEng or higher in Chemical/Process/Mechanical engineering with 2+ years of related experience, with direct biopharmaceutical equipment exposure preferred. On-site role offering growth in a fast-paced, regulated environment.

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