Biotech Project Engineer - Onsite GMP Start-Up Lead

PE Global

Leinster

On-site

EUR 60,000 - 80,000

Full time

8 days ago

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Job summary

PE Global is recruiting a Project Engineer for a leading multinational Biotech client based in Dundalk, Ireland. This is an initial 12-month contract position, full-time onsite, supporting commissioning and qualification of a drug substance and drug product manufacturing facility.

The role focuses on delivering project deliverables, coordinating stakeholders, and ensuring equipment systems pass OQ/PQ/PPQ milestones within GMP operations.

Qualifications

  • Minimum qualification B.Sc. or M.Sc./M.Eng Degree in Engineering (Preferably Chemical Engineering).
  • Process Engineering demonstrated experience.
  • 5 years post academic engineering experience in GMP processing design and start-up environment.
  • Demonstrated ability to be a Project Lead
  • Demonstrated ability to be a team player
  • Excellent communication/presentation/organizational skills.

Responsibilities

  • Prepare project deliverables such as schedules, work plans, equipment cost tracking.
  • Coordinate project activities between stakeholders.
  • Manage installation/start-up/testing of key equipment systems through OQ completion.
  • Interface with cross-functional team to ensure post-OQ readiness (PQ, PPQ).
  • Monitor costs and progress of milestones and report status to stakeholders.
  • Support cross-functional teams to reflect inputs in design deliverables.
  • Liaise with stakeholders, vendors, and SMEs across sites to support the project.

Skills

Process Engineering
Project Leadership
Teamwork
Communication

Education

BSc or MSc Engineering

Job description

PE Global is recruiting a Project Engineer for a leading multinational Biotech client based in Dundalk, Ireland. This is an initial 12-month contract position, full-time onsite, supporting commissioning and qualification of a drug substance and drug product manufacturing facility.

The role focuses on delivering project deliverables, coordinating stakeholders, and ensuring equipment systems pass OQ/PQ/PPQ milestones within GMP operations.

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