Process Engineer

Perrigouk; Braunton; On-site; GBP 45,000 - 62,000; Full time

Job summary

Perrigouk in Braunton, UK, seeks a Process Engineer to join our Process Engineering Team at the Braunton manufacturing site. You will design, implement and optimize processes used in the production of oral solid dose products, ensuring efficiency, safety, cost-effectiveness and regulatory compliance.

Reporting to the Process & Project Engineering Manager, the role requires a degree in engineering and 3+ years in process engineering within manufacturing; pharma experience with cGMP is preferred.

Qualifications

• Degree in engineering or related field.
• 3+ years in a Process Engineering role in manufacturing.
• Experience in oral solid dose/pharmaceutical manufacturing is preferred.
• Experience with process optimisation is required.
• Experience writing technical reports is preferred.

Responsibilities

• Design, implement and optimise manufacturing processes.
• Oversee process changes and change management.
• Ensure compliance with EHS, Quality and regulatory requirements.
• Support production with troubleshooting and improvements.
• Contribute to SOPs, validation protocols and reports.

Skills

Process optimisation

Lean Six Sigma

Regulatory compliance

Technical writing

Cross-functional collaboration

Education

Bachelor's degree in engineering

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 prioritised
• 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