Senior Manufacturing Engineer: GMP, Lean & Process Optimization

Biopharma Careers

Limerick

Hybrid

EUR 52,000 - 83,000

Full time

8 days ago

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Benefits offered by this job

Annual bonus
Vacation days
Parental leave
Bereavement leave
Well-being reimbursement
Insurance plans

Job summary

Johnson & Johnson in Limerick, Ireland, is seeking a Senior Manufacturing Engineer to support manufacturing operations in a regulated environment. You will monitor processes, resolve issues, and drive improvements with cross-functional teams while ensuring safety and compliance.

The role emphasizes validation, change control, and documentation aligned with site quality requirements. 2+ years of engineering experience and a relevant engineering degree are required.

Qualifications

  • Bachelor's degree in an engineering discipline related to manufacturing.
  • At least 2 years of post-qualification engineering experience.
  • Strong problem-solving and independent working abilities.
  • Clear communication and teamwork across functions.

Responsibilities

  • Monitor process performance and resolve equipment or process issues.
  • Support process improvements to safety, quality, yield and efficiency.
  • Collaborate with operations, quality and maintenance to implement solutions.
  • Participate in troubleshooting, root cause analysis and corrective actions.
  • Support validation, change control, and documentation per site quality.
  • Contribute to continuous improvement projects and new equipment introductions.

Skills

Problem solving
Communication
Teamwork
Documentation

Education

Bachelor's degree in Manufacturing/Mechanical/Industrial/Process/Automation Engineering

Tools

GMP
Lean manufacturing
MSAT
Project scheduling tools

Job description

Johnson & Johnson in Limerick, Ireland, is seeking a Senior Manufacturing Engineer to support manufacturing operations in a regulated environment. You will monitor processes, resolve issues, and drive improvements with cross-functional teams while ensuring safety and compliance.

The role emphasizes validation, change control, and documentation aligned with site quality requirements. 2+ years of engineering experience and a relevant engineering degree are required.

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