Pharma Process Engineer: Lean, GMP & Optimization

Perrigouk

Braunton

On-site

GBP 55,000 - 80,000

Full time

10 days ago

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Job summary

Perrigouk in Braunton is seeking a Process Engineer to join the Process Engineering Team at our manufacturing site. The role focuses on designing, implementing and optimising production processes for oral solid dose products, ensuring operations are efficient, safe, cost-effective and compliant with regulatory standards.

We require a Degree in engineering and 3+ years in a process engineering role within manufacturing, with preference for pharma and cGMP experience.

Qualifications

  • Degree in engineering (required).
  • 3+ years in a Process Engineering role within manufacturing (required).
  • Experience in oral solid dose pharmaceutical manufacturing (preferred).
  • Experience with process optimisation (required).
  • Experience writing technical reports (required).
  • Experience in a highly regulated industry (preferred).
  • Experience with industrial building services (preferred).
  • Experience with cGMP environment (preferred).

Responsibilities

  • Identify opportunities for process optimisation.
  • Design process changes and realise opportunities.
  • Conduct engineering change management activities.
  • Contribute to preliminary financial analyses of improvements.
  • Evaluate improvements and oversee implementation.
  • Ensure processes meet regulatory requirements (EHS, Quality).
  • Provide production support with maintenance, production, quality teams.
  • Apply Lean Six Sigma to reduce waste and improve efficiency.
  • Contribute to SOPs, validation protocols and technical reports.

Skills

Process engineering
Lean Six Sigma
Regulatory compliance
Technical reporting

Education

Degree in engineering

Job description

Perrigouk in Braunton is seeking a Process Engineer to join the Process Engineering Team at our manufacturing site. The role focuses on designing, implementing and optimising production processes for oral solid dose products, ensuring operations are efficient, safe, cost-effective and compliant with regulatory standards.

We require a Degree in engineering and 3+ years in a process engineering role within manufacturing, with preference for pharma and cGMP experience.

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