Process Engineer

Perrigouk; Braunton; On-site; GBP 45,000 - 65,000; Full time

Job summary

Perrigouk is seeking a Process Engineer to join the Process Engineering Team at our Braunton manufacturing site. You will design, implement and optimise processes for oral solid dose products, ensuring safety, cost-effectiveness and regulatory compliance.

The role reports to the Process & Project Engineering Manager and involves collaboration across maintenance, production, quality and capital projects, applying Lean and Six Sigma to improve efficiency and reduce waste.

Qualifications

• Degree in a relevant engineering discipline.
• 3+ years of process engineering experience in a manufacturing environment.
• Experience in an oral solid dose pharmaceutical manufacturing environment preferred.
• Experience with process optimisation.
• Experience writing technical reports.
• Experience working in a highly regulated industry preferred.
• Experience with industrial building services preferred.
• Experience working in a cGMP environment preferred.

Responsibilities

• Achieve and maintain expert process and equipment knowledge within a specific area of manufacturing.
• Identify opportunities for process optimisation and implement changes.
• Conduct engineering change management to assess proposed process changes.
• Contribute to preliminary financial analysis of improvements to quantify benefit.
• Evaluate potential improvements and oversee implementation of changes.
• Ensure processes meet EHS, Quality and other regulatory requirements.
• Collaborate with Maintenance, Production, Quality and Capital Project teams to design, implement and maintain production equipment and systems.
• Write technical reports and contribute to SOPs and validation protocols.

Skills

Process Engineering

Lean Six Sigma

Regulatory Compliance

Documentation

Education

Engineering degree

Job description

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We are excited to be recruiting for a Process Engineer to join our Process Engineering Team based in our Braunton manufacturing site.

This position will suit an engineering professional who is seeking a new challenge and has the technical capability, ingenuity and drive to make a difference by identifying and implementing process improvements.

This position reports to the Process & Project Engineering Manager.

In this role you will be responsible for designing, implementing, and optimizing processes used in the production of pharmaceutical oral solid dose products. You will help ensure that manufacturing operations are efficient, safe, cost-effective and compliant with regulatory standards.

Scope of the Role

Process Subject Matter Expert:

• Achieveandmaintainexpertprocess and equipmentknowledgewithina specific area ofmanufacturing

Process Design and Optimisation:

• Identifyopportunities forprocessoptimisation
• Design process changes to realise the identified opportunities
• Conduct engineering change management activities to assess proposed process changes
• Contribute to pre-liminary financial analysis of improvements to quantify benefit
• Evaluate potential improvements to ensure the most beneficial are prioritized
• Oversee implementation of changes

Regulatory Compliance:

• Ensure processes meetEHS, Quality and other regulatory requirements
• Conduct process and equipment assessments to identify risks and implement corrective actions

Production Support:

• Work withMaintenance,Production, Quality andCapitalProject teamsto design, implementandmaintainproduction equipment and systems
• Investigate and troubleshoot production issues and implement corrective actions
• Apply Lean and Six Sigma principles to enhance efficiency and reduce waste

Documentation:

• Contribute to the EngineeringDocumentation/Drawing managementsystem
• Contribute to the development of SOPs, validation protocols and user requirement specification
• Write technical reports

Experience Required

• Degree in a relevant engineering discipline required
• 3+ years of experience in a Process Engineering related role within a manufacturing environment required
• Experience working in an oral solid dose pharmaceutical manufacturing environment preferred
• Experience with process optimisation required
• Experience writing technical reports required
• Experience working in a highly regulated industry preferred
• Experience with industrial building services preferred
• Experience working in a cGMP environment preferred