Process Engineer

Manpower - Ireland

Waterford

On-site

EUR 65,000 - 90,000

Full time

9 days ago

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Job summary

Manpower - Ireland in Waterford seeks a Process Development Engineer (Shift) to lead process optimisation and support manufacturing operations at a GMP-regulated pharmaceutical site. The role involves driving improvement initiatives, troubleshooting complex challenges, and supporting technology transfers and new product introductions.

The ideal candidate has a degree in chemical/industrial/pharmaceutical engineering with proven pharma manufacturing experience and strong problem-solving skills.

Qualifications

  • Degree in Chemical Engineering, Industrial Engineering, Pharmaceutical Engineering, or a related discipline.
  • Proven experience within pharmaceutical manufacturing, process development, process engineering, or technical operations.
  • Strong troubleshooting, root cause analysis, and structured problem-solving skills.
  • Experience leading improvement projects in a regulated manufacturing environment.
  • Advanced degree in Pharmaceutics, Pharmacy, or a related scientific discipline (Desirable).
  • Experience with aseptic manufacturing and lyophilisation (Desirable).
  • Knowledge of DoE, statistical analysis, and pharmaceutical product development (Desirable).
  • Project management experience and stakeholder engagement skills (Desirable).

Responsibilities

  • Lead process optimisation and continuous improvement initiatives across manufacturing operations.
  • Provide technical leadership and support to operations teams.
  • Drive root cause investigations, problem-solving activities, and CAPA implementation.
  • Identify and implement opportunities to improve efficiency, quality, and cycle times.
  • Support capital projects, process development programmes, and plant trials.
  • Act as a Subject Matter Expert for manufacturing processes, product quality attributes, and critical process parameters.
  • Support new product introductions, clinical supply projects, product enhancements, and technology transfers.
  • Develop and monitor key performance metrics.
  • Collaborate with internal and external stakeholders to improve manufacturing and development operations.
  • Ensure all activities comply with GMP requirements.

Skills

Troubleshooting
Root cause analysis
Problem solving
Technical leadership
Process development

Education

Bachelors in Chemical/Industrial/Pharmaceutical Engineering
Advanced degree in Pharmaceutics/Pharmacy

Job description

Process Development Engineer (Shift)

Location: Waterford, Ireland
Shift Pattern: 24/7 Continental Shift (2 Days, 2 Nights, 4 Days Off)


The Opportunity

We are looking for experienced Process Development Engineers to join our clients Waterford manufacturing site. This role is ideal for candidates with a strong background in pharmaceutical manufacturing, process development, technical operations, or engineering support who are looking to take ownership of key improvement initiatives and drive operational excellence.

As a technical leader, you will support manufacturing operations, lead process optimisation projects, troubleshoot complex manufacturing challenges, and play a critical role in new product introductions, technology transfers, and continuous improvement programmes.

Key Responsibilities
  • Lead process optimisation and continuous improvement initiatives across manufacturing operations.

  • Provide technical leadership and support to operations teams.

  • Drive root cause investigations, problem-solving activities, and CAPA implementation.

  • Identify and implement opportunities to improve efficiency, quality, and cycle times.

  • Support capital projects, process development programmes, and plant trials.

  • Act as a Subject Matter Expert for manufacturing processes, product quality attributes, and critical process parameters.

  • Support new product introductions, clinical supply projects, product enhancements, and technology transfers.

  • Develop and monitor key performance metrics.

  • Collaborate with internal and external stakeholders to improve manufacturing and development operations.

  • Ensure all activities comply with GMP requirements.

About You
Essential
  • Degree in Chemical Engineering, Industrial Engineering, Pharmaceutical Engineering, or a related discipline.

  • Proven experience within pharmaceutical manufacturing, process development, process engineering, or technical operations.

  • Strong troubleshooting, root cause analysis, and structured problem-solving skills.

  • Experience leading improvement projects in a regulated manufacturing environment.

Desirable
  • Advanced degree in Pharmaceutics, Pharmacy, or a related scientific discipline.

  • Experience with aseptic manufacturing and lyophilisation.

  • Knowledge of Design of Experiments (DoE), statistical analysis, and pharmaceutical product development.

  • Project management experience and strong stakeholder engagement skills.

Why Apply?
  • Join a leading pharmaceutical manufacturing site.

  • Work on high-impact process improvement and development projects.

  • Influence manufacturing performance, product quality, and operational excellence.

  • Competitive salary plus shift premium.

  • Excellent opportunities for career growth and development.

We're particularly interested in hearing from experienced pharmaceutical engineers and technical specialists who have a proven track record of delivering process improvements and supporting manufacturing excellence in GMP-regulated environments.

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